WO2003093300A2 - Peptides anti-microbiens et compositions - Google Patents

Peptides anti-microbiens et compositions Download PDF

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Publication number
WO2003093300A2
WO2003093300A2 PCT/US2003/014240 US0314240W WO03093300A2 WO 2003093300 A2 WO2003093300 A2 WO 2003093300A2 US 0314240 W US0314240 W US 0314240W WO 03093300 A2 WO03093300 A2 WO 03093300A2
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WIPO (PCT)
Prior art keywords
cyclic peptide
amino acid
peptide
amino acids
pharmaceutical composition
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PCT/US2003/014240
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English (en)
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WO2003093300A3 (fr
Inventor
M. Reza Ghadiri
Hui Sun Kim
Sara Fernandez-Lopez
Keith Wilcoxen
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The Scripps Research Institute
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Priority claimed from PCT/US2002/014329 external-priority patent/WO2002090503A2/fr
Application filed by The Scripps Research Institute filed Critical The Scripps Research Institute
Priority to AU2003228896A priority Critical patent/AU2003228896A1/en
Publication of WO2003093300A2 publication Critical patent/WO2003093300A2/fr
Publication of WO2003093300A3 publication Critical patent/WO2003093300A3/fr

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/64—Cyclic peptides containing only normal peptide links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/50—Cyclic peptides containing at least one abnormal peptide link
    • C07K7/54—Cyclic peptides containing at least one abnormal peptide link with at least one abnormal peptide link in the ring
    • C07K7/56—Cyclic peptides containing at least one abnormal peptide link with at least one abnormal peptide link in the ring the cyclisation not occurring through 2,4-diamino-butanoic acid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Definitions

  • the present invention provides cyclic peptide anti-microbials.
  • Anti- microbial peptides and compositions ofthe invention can quickly kill microbes causing an infection without causing substantial or undesired harm to mammalian cells.
  • the cyclic peptides ofthe invention may be composed of a sequence of ⁇ -amino acids that have a repeating D, L-backbone chirality, or homochiral
  • New antibiotics are often structurally related to, or structurally derived from, a previous generation of antibiotics.
  • cephalosporin is structurally related to penicillin. While these structural analogs of known antibiotics can be successful for a time, increasing reports of resistance often develop as the "new" antibiotic becomes widely used. The progression of ⁇ - lactam antibiotics illustrates this problem. Since the introduction of penicillin in the 1940's, microbes have evolved resistance to /3-lactam antibiotics, typically by acquired or enhanced catabolism of these drugs through the enzyme ⁇ - lactamase that is found in many bacterial strains.
  • valinomycin is a cyclic depsipeptide with an alternating D-D-L-L chiral motif that employs ester linkages within the ring structure.
  • the activity, selectivity, in vivo stability, toxicity and bioavailability of valinomycin and other such peptides are not optimal. Accordingly, there is a need for fast-acting, non-toxic anti-microbial agents to combat microbial infections, especially infections that are resistant to currently available antibiotics, which are easily and cheaply manufactured.
  • the present invention provides new, fast-acting anti-microbial cyclic peptides and compositions for treating and/or preventing microbial infections.
  • the present anti-microbial agents are highly effective for many microbial species, including multiply drug-resistant bacteria as well as lethal methicillin- resistant and vancomycin-resistant microbial strains.
  • Cyclic peptides are fast acting, proteolytically stable and easy to synthesize. In many embodiments, substantially no microbes can be detected within just a few hours of exposure to the cyclic peptides ofthe invention. Still others do not cause substantial undesired lysis of mammalian cells, for example, as measured by hemolysis of erythrocytes.
  • the invention provides anti-microbial cyclic peptides and pharmaceutical compositions thereof for human and veterinary applications wherein the cyclic peptides comprise a sequence of from four to about sixteen alternating D- and L- ⁇ -amino acids, and wherein the cyclic peptide has preferential cytotoxic activity against the target microbial organism and does not have substantial undesired activity against mammalian cells. Activity against mammalian cells can be measured, for example, by the ability of peptides to cause hemolysis of mammalian red blood cells.
  • Such cyclic peptides and pharmaceutical compositions can be used for treating or preventing a microbial infection in a mammal.
  • preferred cyclic peptides ofthe invention have been shown to be bactericidal, and not merely bacteriostatic at minimum inhibitory concentrations.
  • the cyclic peptides ofthe invention generally have a minimum inhibitory concentration at which substantially no cells of at least one target microbe grow in vitro that is less than one half the peptide concentration needed to cause 50% hemolysis of mammalian red blood cells.
  • the minimum inhibitory concentration can be less than one quarter to less than one fifth the peptide concentration needed to cause 50% hemolysis of mammalian red blood cells.
  • the minimum inhibitory concentration is less than at least one tenth to less than at least one twentieth the peptide concentration needed to cause 50% hemolysis of mammalian red blood cells.
  • the target microbial organism can be a bacterial strain, a yeast strain, a fungal strain, a single-cell organism, a single- cell parasite or a related organism.
  • the target microbial organisms are gram-positive bacteria or gram-negative bacteria.
  • the cyclic peptides ofthe invention are believed to self-assemble into supramolecular structures within or by association with microbial membranes.
  • Such supramolecular structures can be, for example, nanotubes, barrels or groups of associated, axially parallel nanotubes, carpets of associated nanotubes, or mixtures thereof.
  • These types of supramolecular structures can induce microbial cell membrane permeation, depolarization or disruption (e.g., lysis) selectively over mammalian cell membrane permeation, depolarization or disruption.
  • Cyclic peptides of the invention may have a plurality of amino acids having side chains with affinity for biomolecules integral to microbial cell membranes.
  • Such biomolecules can facilitate selective assembly ofthe cyclic peptides into supramolecular structures on or within microbial membranes.
  • Most mammalian cell membranes generally do not have the same biomolecular composition as most microbial membranes.
  • Cyclic peptides ofthe invention will not preferably associate with mammalian cell membrane over microbial cell membranes at desired anti-microbial concentrations.
  • the cyclic peptides can have a half- life in the bloodstream ofthe mammal of about six hours or less, at an amount that is effective against microbial infections.
  • Such an effective amount is an amount ofthe cyclic peptide that is sufficient to induce death or lysis of microbial cells in single or divided doses without inducing an undesired amount of death or lysis of mammalian cells.
  • Preferred cyclic peptides ofthe invention induce substantially no hemolysis of red blood cells at anti-microbially effective doses.
  • the cyclic peptides ofthe invention can be admimstered in a single dosage and yet are effective for treating microbial infections.
  • the cyclic peptides ofthe invention can be administered continuously or in multiple doses over a period of one to ten days.
  • Effective amounts ofthe present cyclic peptides include about 0.1 mg/kg to about 100 mg/kg of body weight, alternatively about 0.5 mg/kg to about 50 mg/kg of body weight, about 1.0 mg/kg to about 30 mg/kg of body weight, and other amounts set forth herein.
  • the cyclic peptides ofthe invention generally have about 25% to about 88% D- and/or L-polar amino acids.
  • the percentage of polar amino acids can be from about 33% or 50% to about 65% or 88% ofthe total number of D- and L-amino acids.
  • an eight residue cyclic peptide ofthe invention can have at least one, alternatively, two to seven polar D- and L-amino acids.
  • Other eight residue cyclic peptides will have three to five polar D- and L-amino acids for example.
  • six residue cyclic peptides ofthe invention can have two to five polar D- and L- amino acids.
  • Other six residue cyclic peptides may have three to four polar D- and L-amino acids. At least one of these polar D- or L-amino acids may be adjacent to at least one other polar D- or L-amino acid. Alternatively, at least one polar D- or L-amino acid may be adjacent only to nonpolar D- or L-amino acids.
  • polar amino acids are available to one of skill in the art.
  • Examples of polar D- and L- ⁇ -amino acids that can be utilized in the peptides of the invention mclude the D- or L-enantiomers of serine, threonine, asparagine, glutamine, aspartic acid, cysteine, homocysteine, glutamic acid, histidine, arginine, lysine, hydroxylysine or ornithine.
  • the cyclic peptides ofthe invention generally have about 25% to about 88% D- and/or L-ionizable amino acids.
  • the percentage of ionizable amino acids can be from about 33% or 50% to about 65% or 88% of the total number of D- and L-amino acids.
  • a six or eight residue cyclic peptide can have at least one, or alternatively two or three or more ionizable D- and/or L-amino acids.
  • the cyclic peptides of the invention can have four to six ionizable D- and/or L-amino acids.
  • Such an ionizable D- or L-amino acid can be adjacent to at least one other polar or ionizable D- or L-amino acid.
  • the cyclic peptides ofthe invention can have at least one ionizable D- or L-amino acid that is adj acent only to nonpolar D- or L-amino acids.
  • ionizable amino acids are available to one of skill in the art and the invention contemplates all such ionizable amino acids.
  • ionizable D- and/or L-amino acids include the D- or L-enantiomers of arginine, aspartic acid, glutamic acid, histidine, lysine, hydroxylysine or ornithine.
  • the cyclic peptides ofthe invention can have nonpolar D- and/or L-amino acid residues.
  • the cyclic peptides ofthe invention generally have about 12% to about 75%) D- and/or L-nonpolar amino acids.
  • the percentage of nonpolar amino acids can be from about 50% to about 67% or 75% ofthe total number of D- and/or L-amino acids.
  • an eight residue cyclic peptide ofthe invention can have at least one, alternatively, two to seven nonpolar D- and/or L-amino acids.
  • Other eight residue cyclic peptides may have three to five nonpolar D- and/or L-amino acids.
  • six residue cyclic peptides ofthe invention have two to five nonpolar D- and/or L-amino acids.
  • Other six residue cyclic peptides may have three to four nonpolar D- and/or L-amino acids. At least one of these nonpolar D- and/or L-amino acids may be adjacent to at least one other nonpolar D- and/or L-amino acid. Alternatively, at least one nonpolar D- or L-amino acid may be adjacent only to polar D- or L-amino acids.
  • nonpolar amino acids are available to one of skill in the art and the invention contemplates all such nonpolar amino acids.
  • nonpolar amino acids include the D- and L-enantiomers of alanine, valine, isoleucine, leucine, methionine, norleucine, phenylalanine, tyrosine or tryptophan.
  • amino acids found naturally in proteins may be used, as well as non-naturally occurring and synthetic amino acids.
  • the cyclic peptides ofthe invention can have an amino acid sequence having formula I:
  • m is an integer ranging from 1 to 7; each p is separately an integer ranging from 0 to 7; each X ls X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , X 8 , X 9 , and X 10 is separately a polar D- or L- ⁇ -amino acid; and each Yi, Y 2 , Y 3 , Y 4 , Y 5 , Y 6 , Y 7 , Y 8 , Y 9 , and Y ]0 is separately nonpolar D- or L- ⁇ -amino acid; and wherein the cyclic peptide has an even number of from four to about sixteen alternating D- and L-a amino acids.
  • the cyclic peptides ofthe invention can have an amino acid sequence having formula II:
  • m is an integer ranging from 1 to 7; each p is separately an integer ranging from 0 to 7; each Xi, X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , and X 8 is separately a polar D- or
  • each Yi, Y 2 , Y 3 , Y 4 , Y 5 , Y 6 , Y 7 , and Y 8 is separately nonpolar D- or L-c-amino acid; and wherein the cyclic peptide has an even number of from four to about sixteen alternating D- and L- ⁇ amino acids.
  • the cyclic peptides ofthe invention can have an amino acid sequence having formula III:
  • m is an integer ranging from 1 to 7; each p is separately an integer ranging from 0 to 7; each Xi, X 2 , X 3 , X , X 5 , X 6 , X 7 , X 8 , X 9 , and Xio is separately a polar D- or L-ce-amino acid; each Yi, Y 2 , Y 3 , Y4, Y5, N6, Y7, Ys, Y9, and Y i0 is separately nonpolar D- or L-cx-amino acid; and wherein the cyclic peptide has an even number of from four to about sixteen alternating D- and L- ⁇ amino acids.
  • the cyclic peptide has an amino acid sequence of formula INa or INb:
  • the cyclic peptide has an amino acid sequence of formula Na or Vb:
  • Va Vb wherein: q is an integer ranging from 2 to 7;
  • Xi and X 2 are separately polar amino acids
  • Yi and Y 2 are separately nonpolar amino acids.
  • sequences may or may not be excluded from the above formulae and associated compositions: cyclo-[-D-Arg-Gln-D-Arg-Ala- D-Trp-Leu- D-Trp-Trp-]; cyclo-[-D-Arg-Gh ⁇ -D-Arg-Leu-D-Trp-Leu- D-Trp-Trp-]; cyclo-[-D-Arg-Gln-D-Arg-Nal-D-Trp-Leu- D-Trp-Trp-]; cyclo-[-D-Arg-Gln-D-Arg-Phe-D-Trp-Leu- D-Trp-Trp-]; or cyclo-[-D-Arg-Gln-D-Arg-Trp-D-Trp-Leu- D-Trp-Trp-] . Cyclic peptides having any ofthe above sequences, however, including any of
  • Cyclic peptides often have, for example, about four to about sixteen D- and L- ⁇ -amino acids. In other embodiments, the cyclic peptides have about six to about ten or twelve D- and L-c-amino acids. In still other embodiments, cyclic peptides of about six or eight D- and L- ⁇ -amino acids are employed.
  • the pharmaceutical compositions of the invention can include an effective amount of at least one ofthe cyclic peptides ofthe invention, or two or more different cyclic peptides ofthe invention. These compositions also include a pharmaceutically effective carrier.
  • the cyclic peptides need not be made from D- or L-C ⁇ -amino acids and can alternatively have a sequence of from three to about ten homochiral ⁇ -amino acids.
  • Such ⁇ -amino acids are available to one of skill in the art.
  • Beta amino acids can be substituted at the - or ⁇ -carbons by one to two substituents.
  • Mono-substituted beta amino acids of either S or R chirality can be employed for the construction of cyclic ⁇ -peptides, provided that the cyclic ⁇ -peptide is homochiral.
  • Disubstituted ⁇ -amino acids employed in the homochiral ⁇ -peptides ofthe present invention have the relative R,R or S,S diastereomeric configuration, provided that the cyclic ⁇ -peptide is homochiral.
  • the ⁇ -amino acids ofthe cyclic ⁇ -peptides ofthe present invention should be homochiral, i.e., the substituents at the ⁇ and/or ⁇ backbone carbons should be all S and/or S,S, or all R and/or R,R.
  • Cyclic peptides having ⁇ -amino acids generally have at least one ⁇ -amino acid with at least one polar side chain. Preferred ⁇ -peptides cause substantially no undesirable lysis of mammalian cells.
  • the cyclic ⁇ -peptides ofthe invention can have an amino acid sequence of formula VI:
  • each p is separately an integer ranging from 0 to 7; each Z ⁇ ,Z 3 , Z 5 , Z 7 , Z 9 , Zn, Z ⁇ 3 , Z 15 , Z ⁇ 7 , and Z ⁇ 9 is separately a monosubstituted ⁇ -amino acid; each Z , Z 4 , Z 6 , Z 8 , Z 10 , Z ⁇ 2 , Z ⁇ 4 , Z ⁇ 6 , Z ⁇ 8 , and Z 2 o is separately a disubstituted ⁇ -amino acid; and wherem the cyclic ⁇ -peptide has a sequence of from three to about ten homochiral ⁇ -amino acids.
  • compositions that include an effective amount of at least one cyclic peptide, or two or more different cyclic peptides, wherein these cyclic peptide(s) have a sequence of from three to about ten homochiral ⁇ -amino acids, for example, as provided by formula NI.
  • the invention also provides a method of treating a microbial infection in humans and other animals, which comprises contacting microbial cells with a cyclic peptide comprising a sequence of from four to about sixteen amino acids, wherein the sequence has alternating D- and L- ⁇ -amino acids, in an amount sufficient to induce microbial cell death without inducing an undesirable amount of mammalian or animal cell death.
  • a cyclic peptide comprising a sequence of from four to about sixteen amino acids, wherein the sequence has alternating D- and L- ⁇ -amino acids, in an amount sufficient to induce microbial cell death without inducing an undesirable amount of mammalian or animal cell death.
  • Such cyclic peptides can alternatively have a sequence of from three to about ten homochiral ⁇ -amino acids.
  • the invention further provides a method of identifying cyclic peptides selectively cytotoxic to a target cell-type comprising screening one or more cyclic peptides for induction of cell death or inhibition of cell growth in target cells without induction of substantial or undesired cell death in a second cell type.
  • cyclic peptides may comprise, for example, an alternating D- and L- ⁇ amino acid sequence of between four and about sixteen amino acids.
  • such cyclic peptides may have a sequence of from three to about ten homochiral ⁇ -amino acids.
  • the invention also provides a method of identifying cyclic peptides selectively cytotoxic to a target cell-type comprising: (a) making a combinatorial library of cyclic peptides, wherein each cyclic peptide in the combinatorial library comprises an alternating D- and L- ⁇ amino acid sequence of between four and about sixteen amino acids; and (b) screening cyclic peptides from the combinatorial library for induction of cell death or inhibition of cell growth in target cells without induction of substantial or undesired cell death in a second cell type.
  • such cyclic peptides may have a sequence of from three to about ten homochiral ⁇ -amino acids.
  • the library can be used to generate single cyclic peptides or mixtures of cyclic peptides. Mixtures of cyclic peptides that show anti-microbial activity can then be further screened to identify one or more anti-microbially active cyclic peptides in one or more ofthe mixtures, which can then be isolated or synthesized and re-tested for induction of cell death or inhibition of cell growth in target cells without induction of substantial or undesired cell death in a second cell type.
  • the invention further provides a method of identifying cyclic peptides selectively cytotoxic to a target cell-type.
  • This method involves the step of rationally designing at least one cyclic peptide comprising an alternating D- and L- ⁇ amino acid sequence of between four and sixteen amino acids.
  • cyclic peptides may have a sequence of from three to about ten homochiral ⁇ -amino acids.
  • the method further involves screening such rationally designed cyclic peptides for induction of cell death or inhibition of cell growth in target cells without induction of substantial or undesired cell death in a second cell type.
  • Rationally designing a cyclic peptide can involve identifying at least one effective cyclic peptide from a combinatorial library that can induce cell death in target cells without inducing substantial or undesired cell death in a second cell type and exchanging at least one amino acid for a different amino acid in the alternating D- and L- ⁇ amino acid sequence ofthe effective cyclic peptide to generate a rationally designed cyclic peptide.
  • the rationally designed cyclic peptide can then be screened for induction of cell death or inhibition of cell growth in target cells without inducing substantial or undesired cell death in a second cell type.
  • such cyclic peptides may have a sequence of from three to about ten homochiral ⁇ -amino acids.
  • the target cell-type can be a microbe and the second cell type can be a mammalian cell, for example, a mammalian red blood cell.
  • Cell death ofthe second cell type can be detected by detecting hemolysis of red blood cells.
  • the above methods can further include screening a third cell type. Such screening can include determining whether a peptide induces substantial or undesired cell death in the third cell type.
  • the method can also mclude determining the minimum inhibitory dose at which a peptide can kill substantially all, or inhibit the growth, ofthe target cells.
  • Screening can be performed in vitro by separately contacting a peptide with the target cell type and with other cell types (e.g., a second or third or other cell type).
  • screening can be performed in vivo by administering at least one peptide to a test animal comprising the target cell type and another cell type or types and determining whether the peptide is toxic to the target cell type but does not have substantial or undesired toxicity to another cell type or types.
  • Such a method can also include determining whether the peptide adversely affects the health ofthe animal. Determining whether the peptide adversely affects the health ofthe animal can include examining the bodily fluids or the anatomy of the animal by pathological or histological methods.
  • the invention further provides a method of identifying cyclic peptides capable of selective association with one or more target biomolecules on a selected cell surface, comprising contacting a solution of cyclic peptides, each peptide comprising between four to about sixteen amino acids in an alternating D- and L- ⁇ amino acid sequence, or a peptide comprising from three to about ten ⁇ -amino acids, with the target biomolecule(s) and determining, for example, whether the peptides spontaneously assemble into a supramolecular structure that selectively associates with the biomolecule(s).
  • the target biomolecule can be displayed, for example, on the surface of a living cell or on the surface of a liposome.
  • the peptide can be contacted with the target biomolecule(s).
  • the method can further include determining the structure ofthe peptides that spontaneously assemble into the supramolecular structure that selectively associates with the biomolecule(s).
  • the present invention also provides methods of evaluating or confirming therapeutically effective dosages for treating a microbial infection with a cyclic peptide having an amino acid sequence of alternating D- and L- ⁇ -amino acids, or a cyclic peptide comprising from three to about ten /3-amino acids, that includes determining the minimum inhibitory concentration ofthe cyclic peptide at which substantially no bacteria grow in vitro.
  • the present invention also provides a composition comprising one or more ofthe present cyclic peptides with one or more other anti-microbial agents.
  • agents include penicillin, vancomycin, erythromycin and other therapeutic agents.
  • Mammals and birds may be treated by the methods and compositions described and claimed herein. Such mammals and birds include humans, dogs, cats, and livestock, for example, horses, cattle, sheep, goats, chickens, turkeys and the like.
  • FIGURES Figure 1 provides a schematic drawing ofthe self-assembly ofthe present cyclic peptides into nanotubules.
  • An eight-residue cyclic D, L- ⁇ -peptide with alternating D- and L-amino acids is depicted to the left, with emphasis on its flat ring-shaped conformation.
  • Side chains (R) decorate the outside surface of the cyclic peptide.
  • a series of cyclic peptides align and are believed to undergo intermolecular hydrogen bonding to form a tubular structure referred to herein as a nanotube (center).
  • Self-assembly is believed to be directed by mter-subunit backbone-backbone hydrogen bonding resulting in a ⁇ - sheet-like open-ended hollow tubular supramolecular structure. This /3-sheet like hydrogen bonding pattern is shown to the right. For clarity most side chains are omitted.
  • Figure 2 illustrates the modes of membrane permeation that are accessible to peptide supramolecular structures.
  • supramolecular structures that may be formed can interact with the membranes of cells through, for example, supramolecular assembly of (a) pores, (b) barrel stave structures, (c) carpet-like structures, or (d) alternate modes of action.
  • Cyclic peptides are depicted as ring structures. Note that in Figure 2b, the hydrophobic tails ofthe membrane lipids interact with hydrophobic portions ofthe nanotubes, whereas in Figure 2d the hydrophilic heads ofthe membrane lipids interact with hydrophilic portions ofthe nanotubes.
  • FIG. 3 graphically illustrates the rate of membrane depolarization of intact S. aureus (ATCC 25923) upon exposure to cyclic peptide SEQ ID NO:8 (open circles), cyclic peptide SEQ ID NO: 18 (open triangles), and cyclic peptide SEQ ID NO:26 (open squares).
  • Membrane depolarization was monitored by the change in the fluorescence emission intensity ofthe membrane potential- sensitive dye diSC3.
  • the excitation wavelength ( ⁇ ) was 622 nm and the emission wavelength ( ⁇ em ) was 670 nm.
  • Figure 4 provides a plot ofthe apparent proton transport (Figure 4a) and the carboxyfluoroscein release ( Figure 4b) mediated by peptide SEQ ID NO:l 1
  • Figure 5 provides an attenuated total reflectance (ATR) infrared (IR) spectra for analyzing the orientation of peptide SEQ ID NO: 11 (cyclo-[-Gln-D- Lys-(Tr ⁇ -D-Leu) 2 -Trp-D-Lys-] in DMPC multibilayers.
  • the solid trace indicates absorbance of parallel-polarized light; the dashed trace provides absorbance of perpendicular-polarized light.
  • Figure 6 provides a dose-effect curve illustrating the in vivo efficacy of three cyclic peptides as anti-microbial compounds.
  • Figure 7 provides a structural comparison of supramolecular structures composed of: (a) cyclic /3-tetrapeptides, and (b) cyclic D, L- ⁇ -octapeptides.
  • This figure illustrates that, due to the unidirectional arrangement ofthe polar backbone amide groups, cyclic /3-tetrapeptide supramolecular structures may possess a macrodipole moment reminiscent of an ⁇ -helix, while cyclic D, L- ⁇ - octapeptide supramolecular structures will, under most circumstances, not have such a net dipole moment.
  • most side chains are omitted from the nanotube structures depicted in Figure 7a and 7b.
  • Figure 8a provides a "time-killing curve" illustrating the number of surviving S. aureus (MRS A, ATCC 33591) in log cfu/ml as a function of time after exposure to one ofthe following peptides at MIC concentrations: cyclo[KHLWLW] (closed circles), cyclo[KRKWLWLW] (closed triangles) or cyclo[KQRWLWLW] (open squares), where the underlining indicates that the amino acid is a D-amino acid.
  • Figure 8b provides a "time-killing curve" illustrating the number of surviving E. coli JM109 (DE3) in log cfu/ml as a function of time after exposure to one ofthe following peptides at the MIC concentration: cyclo[KRKWLWLW] (closed triangles), cyclo[KORWLWLW] (closed circles), cyclo[KHLWLW] (closed squares) or cyclo[K LWLW] (open squares), where the underlining indicates that the amino acid is a D-amino acid.
  • Figure 9 provides a "time-killing curve" illustrating the number of surviving S. aureus (MRSA) (ATCC 33592)(log cfu/ml) as a function of time after exposure to the cyclo[KSKWLWLW] peptide at 37 °C, where the underlining indicates that the amino acid is a D-amino acid. The effects of several concentrations ofthe cyclo[KSKWLWLW] peptide on separate cultures are shown.
  • Figure 10 provides a "time-killing curve" illustrating the number of surviving S. aureus (MRS A) (ATCC 33592)(log cfu/ml) as a function of time after exposure ofthe cyclo[KSKWLWLW] peptide at room temperature, where the underlining indicates that the amino acid is a D-amino acid. The effects of several concentrations ofthe cyclo[KSKWLWLW] peptide on separate cultures are shown.
  • Figure 11 provides a "time-killing curve" illustrating the number of surviving Enterococcus faecium SP180 (cfu/ml) as a function of time after exposure to the cyclo[KSKWLWLW] peptide at 37 °C, where the underlining indicates that the amino acid is a D-amino acid.
  • E. faecium SP180 is vancomycin resistant (vanA) and multiply resistant to several FDA approved antibiotics. The effects of several concentrations ofthe cyclo[KSKWLWLW] peptide on separate cultures are shown.
  • Figure 12 provides a "time-killing curve" illustrating the number of surviving Enterococcus faecium SP180 (cfu/ml) as a function of time after exposure t the cyclo[KSKWLWLW] peptide at room temperature, where the underlining indicates that the amino acid is a D-amino acid.
  • E. faecium SP180 is vancomycin resistant (vanA) and multiply resistant to several FDA approved antibiotics. The effects of several concentrations ofthe cyclo[KSKWLWLW] peptide on separate cultures are shown.
  • Figure 13 provides a "time-killing curve" illustrating the number of surviving S. aureus (MRS A) (ATCC 33592)(cfu/ml) as a function of time after exposure to the cyclo[RRKWLWLW] peptide at 37 °C, where the underlining indicates that the amino acid is a D-amino acid. The effects of several concentrations ofthe cyclo[RRKWLWLW] peptide on separate cultures are shown.
  • Figure 14 provides a "time killing curve" illustrating the number of surviving S. aureus (MRSA) (ATCC 33592)(cfu/ml) as a function of time after exposure to the cyclo[RRKWLWLW] peptide at room temperature, where the underlining indicates that the amino acid is a D-amino acid. The effects of several concentrations ofthe cyclo[RRKWLWLW] peptide on separate cultures are shown.
  • MRSA MRSA
  • Figure 15 provides a "time-killing curve" illustrating the number of surviving Eneterococus faecium SP180 (cfu/ml) as a function of time after exposure to the cyclo[RRKWLWLW] peptide at 37 °C, where the underlining indicates that the amino acid is a D-amino acid.
  • E. faecium SP180 is vancomycin resistant (vanA) and multiply resistant to several FDA approved antibiotics. The effects of several concentrations ofthe cyclo[RR WLWLW] peptide on separate cultures are shown.
  • Figure 16 provides a "time-killing curve" illustrating the number of surviving Eneterococus faecium SP180 (cfu/ml) as a function of time after exposure to the cyclo[RRKWLWLW] peptide at room temperature, where the underlining indicates that the amino acid is a D-amino acid.
  • E. faecium SP180 is vancomycin resistant (vanA) and multiply resistant to several FDA approved antibiotics. The effects of several concentrations ofthe cyclo[RRKWLWLW] peptide on separate cultures are shown.
  • Figure 17 provides a "time-killing curve" illustrating the number of surviving S. aureus (MRS A) (ATCC 33592)(cfu/ml) as a function of time after cells were exposed to penicillin G at 37 °C. The effects of several concentrations penicillin G on separate cultures are shown.
  • MRS A S. aureus
  • Figure 18 provides a "time-killing curve” illustrating the number of surviving S. aureus (MRSA) (ATCC 33592)(cfu/ml) as a function of time after cells were exposed to penicillin G at room temperature. The effects of several concentrations of penicillin G on separate cultures are shown.
  • Figure 19 provides a "time-killing curve” illustrating the number of surviving Eneterococus faecium SP180 (cfu/ml) as a function of time after cells were exposed to penicillin G at 37 °C.
  • E. faecium SP180 is vancomycin resistant (vanA) and multiply resistant to several FDA approved antibiotics. The effects of several concentrations penicillin G on separate cultures are shown.
  • Figure 20 provides a "time-killing curve" illustrating the number of surviving Eneterococus faecium SP180 (cfu/ml) as a function of time after cells were exposed to penicillin at room temperature.
  • E. faecium SP180 is vancomycin resistant (vanA) and multiply resistant to several FDA approved antibiotics. The effects of several concentrations of penicillin on separate cultures are shown.
  • Figure 21 provides a thin section electron microscopy image of untreated S. aureus (ATCC 25923) displaying a normal intact membrane.
  • Figure 22 provides a thin section electron microscopy image of S. aureus (ATCC 25923) after exposure to 2XMIC concentration of cyclo[KSKWLWLW] for 2 h.
  • the image provides direct visualization ofthe membrane mode of action. Arrows denote abnormal membrane structures caused by the peptide action.
  • Figure 23 provides a thin section electron microscopy image of S. aureus (ATCC 25923) after exposure to 2xMIC concentration of cyclo[KSKWLWLW] for 2 h.
  • the image provides direct visualization ofthe membrane mode of action. Arrows denote abnormal membrane structures caused by the peptide action.
  • Figure 24 illustrates the protective effects ofthe present cyclic peptides on survival of mice lethally infected with S. aureus MRSA (ATCC 33591).
  • the mouse peritonitis model was used with intraperitoneal infection (right side) of bacteria in 5 % mucin and peptide injection (IP left side) 45-60 min post infection. Survival was monitored over 14 days (death as an end point); eight mice were tested per dose.
  • the mice were injected with varying concentrations of cyclo[RRKWLWLW]HCl.
  • Figure 24b the mice were injected with varying concentrations of cyclo[KQRWLWLW]HCl.
  • Figure 25 illustrates the protective effects ofthe present cyclic peptides on survival of mice infected with S. aureus MRSA (ATCC 33591).
  • the mouse peritonitis model was used with intraperitoneal infection (right side) of bacteria in 5 % mucin and peptide injection (IP left side) 45-60 min post infection. Survival was monitored over 14 days (death as an end point); eight mice were tested per dose.
  • Figure 25a the mice were injected with varying concentrations of cyclo[KSKWLWLW]HCl.
  • Figure 25b the mice were injected with varying concentrations of cyclo[KKKWLWLW]HCl.
  • Figure 26 illustrates the protective effects ofthe present cyclic peptides on survival of mice infected with S.
  • aureus MRSA ATCC 33591.
  • the mouse peritonitis model was used with intraperitoneal infection (right side) of bacteria in 5 % mucin and peptide injection (IP left side) 45-60 min post infection. Survival was monitored over 14 days (death as an end point); eight mice were tested per dose. The mice were injected with varying concentrations of cyclo[KKLWLW]HCl.
  • Figure 27 illustrates the protective effects ofthe present cyclic peptides on survival of mice infected with vancomycin resistant E. faecium (NR ⁇ F)(ATCC 51575).
  • the mouse peritonitis model was used with intraperitoneal infection (right side) of bacteria in 5 % mucin and peptide injection (IP left side) 45-60 min post infection. Survival was monitored over 14 days (death as an end point); eight mice were .tested per dose, l Figure 27a, the mice were injected with varying concentrations of cyclo[RRKWLWLW]HCl. In Figure 27b, the mice were injected with varying concentrations of cyclo[KSKWLWLW]HCl.
  • Figure 28 illustrates the protective effects ofthe present cyclic peptides on survival of mice infected with S. aureus MRSA (ATCC 33591).
  • the mouse peritonitis model was used with intraperitoneal infection (right side) of bacteria in 5 % mucin and peptide injection (IP left side) 45-60 min post infection. Survival was monitored over 14 days (death as an end point); four mice were tested per dose.
  • the mice were injected subcutaneously (upper neck compartment) with varying concentrations of cyclo[RRKWLWLW]HCl.
  • Figure 28b the mice were injected intravenously with varying concentrations of cyclo[RRKWLWLW]HCl.
  • Peptide doses indicated are for each injection. Five doses at the indicated mg/kg quantities were administered intravenously 8- 12 h apart.
  • Figure 29 illustrates the toxicity of peptides administered via intraperitoneal route.
  • the mice were injected with varying concentrations of cyclo[RRKWLWLW]HCl.
  • the mice were injected with varying concentrations of cyclo[KQRWLWLW]HCl. Mice were monitored over a period of 14 days for activity and mortality. Four mice per dose were used in each experiment.
  • Figure 30 illustrates the toxicity of peptides administered via intraperitoneal route.
  • the mice were injected with varying concentrations of cyclo[KSKWLWLW]HCl.
  • the mice were injected with varying concentrations of cyclo[KKLWLW]HCl. Mice were monitored over a period of 14 days for activity and mortality. Four mice per dose were used in each experiment.
  • the present invention provides small cyclic peptides and compositions that quickly and selectively kill microbes without substantial or undesired toxicity toward mammalian cells.
  • the present invention includes cyclic peptides, and pharmaceutical compositions comprising cyclic peptides, with either a sequence of alternating D-, and L- ⁇ -amino acids, or a sequence of ⁇ - amino acids, that can sample flat, ring-shaped conformations.
  • Such ring-shaped conformations project the amino acid side chains ofthe cyclic peptides away from the center ofthe ring and orient the amide backbone approximately perpendicular to the plane ofthe ring structure.
  • the cyclic peptides can self-assemble via intermolecular hydrogen bonding to form supramolecular structures.
  • Cyclic peptides that simply contain one or more D-amino acids do not adopt a flat ring-shaped conformation and do not have the backbone conformation needed for self-assembly ofthe cyclic peptide into supramolecular structures.
  • Target microbial organisms against which the present cyclic peptides are effective include microbes, including any single cell organism or parasite that has a cellular membrane and that can infect a mammal.
  • target microbial organisms include bacteria, fungi, helminths, protozoa, yeast strains and other single cell organisms.
  • Cyclic peptides ofthe invention have been found to be active against both gram-negative and gram-positive bacteria. Small differences in environment, for example, the difference in composition of different cellular membranes, can influence the course and nature ofthe proposed assembly process. This feature is used in the present invention both to target and to optimize the anti-microbial activity of selected cyclic peptides against particular microbial species, while providing substantially no toxicity, or no undesired toxicity, in mammalian cells at therapeutically effective doses and dose regimens.
  • Supramolecular structures are believed to respond to their immediate environment through dynamic self-assembling/disassembling processes to quickly find the most thermodynamically favored assembly. It is believed that, during assembly, peptide supramolecular structures sense and respond to the environment of a cellular membrane by sampling various topologically related assemblies. In non-target mammalian membranes at therapeutically desirable concentrations, it is believed that the preferred cyclic peptides ofthe invention do not or cannot adopt a thermodynamically favorable supramolecular structure. Thus, mammalian membranes are not substantially or undesirably affected by the presence of such cyclic peptides.
  • the present cyclic peptides are believed to form unique energetically favorable supramolecular structures that destabilize (e.g., lyse), penneabilize and/or depolarize the microbial membrane, thereby disrupting microbial transmembrane ion and electrical gradients and other vital functions, and quickly leading to microbial cell death.
  • Another feature ofthe present self-assembling peptide supramolecular structures is believed to be the potential for a given cyclic peptide to form a number of diastereomeric nanotube assemblies. This property stems from the fact that backbone-backbone hydrogen bonding are believed primarily to direct the self-assembly ofthe nanotube structure. Differently stacked subunits can give rise to topoisomeric supramolecular structures that share the same or nearly the same tubular /3-sheet-like hydrogen bonded backbone structure. The variety of supramolecular structures assembled from a single cyclic peptide minimizes the probability that microbes can develop resistance to these antibiotic agents.
  • a multitude of cyclic peptides can quickly be screened or evaluated for the ability to selectively target and assemble in microbial membranes. They can also be screened and evaluated for anti-microbial activity by testing for increased membrane permeability, depolarization, or destabilization.
  • amino acid includes the residues ofthe natural ⁇ -amino acids (e.g. Ala, Arg, Asn, Asp, Cys, Glu, Gin, Gly, His, Hyl, Hyp, He, Leu, Lys, Met, Phe, Pro, Ser, Thr, Trp, Tyr, and Nal) in D or L form, as well as /3-amino acids, synthetic and unnatural amino acids.
  • ⁇ -amino acids e.g. Ala, Arg, Asn, Asp, Cys, Glu, Gin, Gly, His, Hyl, Hyp, He, Leu, Lys, Met, Phe, Pro, Ser, Thr, Trp, Tyr, and Nal
  • amino acids that can be utilized in the cyclic peptide described herein can be found, for example, in Fasman, 1989, CRC Practical Handbook of Biochemistry and Molecular Biology, CRC Press, Inc., and the references cited therein. Another source of a wide variety of amino acid residues is provided by the website of RSP Amino Acids Analogues, Inc. (www.amino-acids.com).
  • mammal refers to an animal, in general, a warm-blooded animal, which is susceptible to or has a microbial infection. Mammals include cattle, buffalo, sheep, goats, pigs, horses, dogs, cats, rats, rabbits, mice, and humans. Also included are other livestock, domesticated animals and captive animals.
  • farm animals includes chickens, turkeys, fish, and other farmed animals.
  • a “nanotube” or “nanotubule” is a small tubule that may spontaneously form from the cyclic peptides ofthe present invention.
  • the present cyclic peptides are believed to stack to form supramolecular structures composed of nanotubes. Hydrogen bonding between cyclic peptide is believed to help drive the self-assembly ofthe supramolecular structures from the cyclic peptide.
  • Each nanotube has a pore in the center ofthe tube that is surrounded by the series of peptide backbones ofthe stacked cyclic peptides that form the nanotubes. The size ofthe pore depends upon the number of amino acids in the cyclic peptides that form the nanotube.
  • ions, sugars, and other small molecules can travel through the pores ofthe nanotubes. Larger molecules can also flow through pores formed from larger cyclic peptides and supramolecular structures formed of aggregates of nanotubes.
  • the supramolecular structure is thought to be a barrel-like structure composed of clusters of nanotubes.
  • the supramolecular structure is thought to be a "carpet” or “carpet-like” arrangement of nanotubes.
  • a “carpet” or “carpet-like” arrangement of one or more nanotubes is where the nanotube(s) adopt orientations that can be approximately or somewhat parallel to the plane of the membrane structure.
  • the nanotubes can assume other orientations relative to the plane ofthe membrane.
  • the nanotubes may be situated on the surface ofthe membrane, or may be partially or fully contained within the interior ofthe membrane.
  • the carpet-like nanotubes can be oriented with a tilt angle of up to approximately 70 ⁇ 5° from the membrane normal.
  • a hydrophilic face of a nanotube can, for example, be positioned so that it is in contact with the hydrophilic portions ofthe membrane or with the aqueous environment.
  • a hydrophobic face of a nanotube can, for example, be in contact with the hydrophobic portions ofthe membrane. See Figure 2A-D.
  • peptide as used herein includes a sequence of from four to sixteen amino acids residues in which the ⁇ -carboxyl group of one amino acid is joined by an amide bond to the main chain ( ⁇ - or ⁇ -) amino group ofthe adjacent amino acid.
  • the peptides provided herein for use in the described and claimed methods and compositions are cyclic. Peptide sequences specifically recited herein are written with the amino terminus on the left and the carboxy terminus on the right. However, where the peptides are shown in cyclic form, the first amino acid in the sequence is arbitrarily chosen. Moreover, for formulae of cyclic peptides where the sequence extends onto two lines, the sequence on the second line extends from the N-terminal side on the right to the C-terminal side on the left.
  • “supramolecular structures” are multi-subunit structures, e.g. nanotubes, barrels and carpets of nanotubules, which are believed to be formed through "noncovalent” assembly of cyclic peptides.
  • Supramolecular structures may be contrasted with molecular or polymeric systems in which the product of covalent bond formation between reactants or monomers.
  • the proposed peptide supramolecular structures are thermodynamically controlled assemblies that can undergo reversible structural assembly and disassembly. Such assembly-disassembly will depend, for example, on the environment, subunit structure, side group selection, side group interaction, and the nature and combination of noncovalent forces operating on the system.
  • compositions containing peptides that can form supramolecular structures are their ability to select amongst various cell membrane types. Such selection is driven by favorable thermodynamic forces determined by the composition ofthe cyclic peptide relative to the cell membrane environment and the molecular and/or supramolecular constituents ofthe cell membrane.
  • substantially no with reference to self-assembly, hemolysis, toxicity or cellular lysis, or the like, means that little or no self-assembly, hemolysis, toxicity, cellular lysis or the like is present at the tested or desired peptide dosage or concentration.
  • substantially no hemolysis can mean that less than about 20%, alternatively less than 15% or less than 10%>, or no detectable, hemolysis at the tested or desired peptide dosage or concentration has occurred.
  • substantially no toxicity or lysis can mean that less than about 20%, alternatively less than 15% or less than 10%, or no detectable, toxicity or lysis at the tested or desired peptide dosage or concentration has occurred.
  • terapéuticaally effective amount is that amount sufficient to control a microbial infection.
  • a therapeutically effective amount generally controls the amount of microbes and/or a disease state characterized by the presence of microbes in the infected mammal, for example, by at least about 20%, by at least about 40%, by at least about 60%, or by at least about 80% relative to untreated subjects.
  • a therapeutically effective amount controls the amount of microbes and/or a disease state characterized by the presence of microbes in the infected mammal by at least about 90% or more.
  • a “therapeutically effective amount” is that amount of cyclic peptide needed to permeabilize, depolarize or destabilize the cellular membrane ofthe target microbial organism causing the infection.
  • the tenn "therapeutically effective amount” can also be the amount needed to kill the target microbial organisms causing the infection.
  • An effective amount ofthe therapeutic agent necessary to control microbes can vary according to factors such as the type of microbes, the amount of microbes already present in the animal, the age, sex, health and weight ofthe mammal, and the ability ofthe cyclic peptides ofthe present invention to control microbial infections in the mammal.
  • Therapeutically effective amounts ofthe peptide and peptide compositions can also be used to prevent microbial infection, including preventing a recurrence of microbial infection.
  • the present invention provides cyclic peptides and compositions including cyclic peptides that have an amino acid sequence of alternating D- and L-amino acids that is between four to about sixteen, alternatively about six to about sixteen amino acids in length.
  • the cyclic peptides ofthe present invention can have between three to about ten /3-amino acids, general, the cyclic D, L- ⁇ -peptides do not include the amino acids proline and glycine.
  • ⁇ -amino acids can be substituted at the ⁇ - or ⁇ -carbons, or both.
  • Mono-substituted ⁇ -amino acids of either S or R chirality can be employed for the construction of cyclic ⁇ -peptides, provided that the cyclic beta peptide is homochiral.
  • Disubstituted ⁇ -amino acids employed in the present invention must have the relative R,R or S,S diastereomeric configuration, provided that the ⁇ -amino acid residues in a cyclic peptide structure are homochiral.
  • Cyclic peptides having ⁇ -amino acids generally have at least one ⁇ - amino acid with at least one polar side chain.
  • the cyclic peptides ofthe present invention are believed to undergo self- assembly to form supramolecular structures that, upon assembly in or on a microbial membrane, can cause depolarization and/or permeablization and/or destabilization ofthe microbial membrane.
  • the cyclic peptides cause lysis ofthe microbe, e.g. a bacterium.
  • Self-assembly into supramolecular structures is thought to occur by stacking ofthe cyclic peptides in an anti-parallel fashion or a parallel fashion with formation of /3-sheet hydrogen bonds between adjacent cyclic peptides.
  • Cyclic peptides ofthe present invention can be made from ⁇ -amino acids or /3-amino acids.
  • the amino acid sequence ofthe present cyclic peptides includes at least one polar amino acid in the case of D,L ⁇ -amino acid cyclic peptides, or at least one polar side chain in the case of cyclic ⁇ -peptides.
  • the percentage of polar amino acids can range, for example, from about 25% or 33% to about 65% or 88%. However, in some embodiments a majority ofthe amino acids are polar. For example, the percentage of polar amino acids can be from about 50% to about 88% ofthe total number of amino acids. The exact number of polar and nonpolar amino acids depends on the size and the properties sought for a given cyclic peptide.
  • the sizes for the present cyclic peptides are about six to about ten D,L ⁇ -amino acids or three to about ten ⁇ - amino acids, h other embodiments, the size for the present cyclic peptides is about six to about eight D,L ⁇ -amino acids or four to about six /3-amino acids.
  • an eight residue cyclic peptide ofthe invention can have at least one, alternatively, two to seven polar D- and/or L- ⁇ -amino acids.
  • Other eight residue cyclic peptides will have three to five polar D- and/or L- ⁇ -amino acids for example.
  • Preferred eight residue cyclic peptides have three, four or five polar amino acids.
  • six residue cyclic peptides ofthe invention can have two to five polar D- and/or L- ⁇ -amino acids.
  • Other six residue cyclic peptides may have three to four polar D- and/or L- ⁇ - amino acids. At least one of these polar D- or L- ⁇ -amino acids may be adjacent to at least one other polar D- or L- ⁇ -amino acid.
  • at least one polar D- or L- ⁇ -amino acid may be adjacent only to nonpolar D- or L- ⁇ -amino acids.
  • Beta peptides having about four to about eight /3-amino acids may have, for example, about two to twelve polar side chains, depending on the level of ⁇ and ⁇ backbone substitution.
  • the cyclic D- L- ⁇ -peptides ofthe invention generally have about 25% to about 88% ionizable amino acid residues.
  • the percentage of ionizable amino acids can be from about 33% or 50% to about 65% or 88% of the total number of D- and/or L-amino acids.
  • a six or eight residue cyclic peptide can have at least one, or alternatively two or three or more ionizable D- and/or L-amino acids, hi other embodiments, the cyclic peptides of the invention can have four to six ionizable D- and/or L-amino acids.
  • Such an ionizable D- or L-amino acid can be adjacent to at least one other polar or ionizable D- or L-amino acid.
  • the cyclic peptides ofthe invention can have at least one ionizable D- or L-amino acid that is adjacent only to nonpolar D- or L-amino acids.
  • the cyclic ⁇ -peptides ofthe invention generally have about 25% to about 88% ionizable amino acid side chains. In some embodiments, the percentage of ionizable amino acid side chains can be from about 33% or 50% to about 65% or 88% ofthe total number of amino acid side chains.
  • a four to six residue cyclic ⁇ -peptide can have at least one, or alternatively two or three or more ionizable amino acid side chains.
  • the cyclic ⁇ -peptides ofthe invention can have four to six ionizable amino acid side chains.
  • the cyclic peptides ofthe invention can have nonpolar D- and/or L-amino acid residues. The number of non-polar amino acids chosen can vary as the size ofthe peptide varies and as the selected microbial membrane environment varies.
  • the cyclic peptides ofthe invention generally have about 12% to about 75% D- and L-nonpolar amino acids.
  • the percentage of nonpolar amino acids can be from about 50% to about 67% or 75% ofthe total number of D- and L-amino acids.
  • an eight residue cyclic peptide ofthe invention can have at least one, alternatively, two to seven nonpolar D- and/or L-amino acids.
  • Other eight residue cyclic peptides may have three to five nonpolar D- and/or L-amino acids.
  • six residue cyclic peptides ofthe invention have two to five nonpolar D- and/or L-amino acids.
  • Other six residue cyclic peptides may have three to four nonpolar D- and/or L-amino acids.
  • At least one of these nonpolar D- or L- amino acids may be adjacent to at least one other nonpolar D- or L-amino acid.
  • at least one nonpolar D- or L-amino acid may be adjacent only to polar D- or L-amino acids.
  • the cyclic peptides do not include the amino acid proline or glycine, but certain cyclic peptides may have good activity even though proline or glycine is included.
  • ⁇ -amino acids can have non-polar side chains at the ⁇ - or ⁇ -carbons, or both.
  • the number of non-polar amino acid side chains chosen can vary as the size ofthe peptide varies and as the selected microbial membrane environment varies.
  • the cyclic ⁇ -peptides ofthe invention generally have about 12% to about 75% nonpolar amino acid side chains.
  • the percentage of nonpolar amino acid side chains can be from about 50%» to about 67% or 75% ofthe total number of amino acid side chains.
  • an eight residue cyclic ⁇ -peptide ofthe invention can have at least one, alternatively, two to seven nonpolar amino acid side chains.
  • Other eight residue cyclic ⁇ -peptides may have three to five nonpolar amino acid side chains.
  • six residue cyclic ⁇ -peptides ofthe invention have two to five nonpolar amino acid side chains.
  • Other six residue cyclic ⁇ -peptides may have three to four nonpolar amino acid side chains.
  • Amino acids used in the cyclic peptides can be genetically encoded amino acids, naturally occurring non-genetically encoded amino acids, or synthetic amino acids. Both L- and D-enantiomers of any ofthe above are utilized in the cyclic peptides.
  • the amino acid notations used herein for the twenty genetically encoded L-amino acids and some examples of non-encoded amino acids are provided in Table 1.
  • Certain commonly encountered amino acids that are not genetically encoded and that can be present in the cyclic peptides ofthe invention include, but are not limited to, -alanine (b-Ala) and other omega-amino acids such as 3- aminopropionic acid (Dap), 2,3-diaminopropionic acid (Dpr), 4-aminobutyric acid and so forth; ⁇ -aminoisobutyric acid (Aib); 6-aminohexanoic acid (Aha); ⁇ - aminovaleric acid (Ava); methylglycine (MeGly); ornithine (Orn); citrulline (Cit); t-butylalanine (t-BuA); t-butylglycine (t-BuG); N-methylisoleucine (Melle); phenylglycine (Phg); cyclohexylalanine (Cha); norleucine (Nle); 2- naphthylalanine (2-Nal); 4-
  • Additional amino acid analogs contemplated include phosphoserine, phosphothreonine, phosphotyrosine, hydroxyproline, ' gamma-carboxyglutamate, hippuric acid, octahydroindole-2-carboxylic acid, statine, ⁇ -methyl-alanine, para-benzoyl-phenylalanine, propargylglycine, and sarcosine.
  • Peptides that are encompassed within the scope ofthe invention can have any of foregoing amino acids in the L- or D- configuration, or any other amino acid known to one of skill in the art.
  • amino acids that are substitutable for each other generally reside within similar classes or subclasses. As known to one of skill in the art, amino acids can be placed into different classes depending primarily upon the chemical and physical properties ofthe amino acid side chain. For example, some amino acids are generally considered to be hydrophilic or polar amino acids and others are considered to be hydrophobic or nonpolar amino acids.
  • Polar amino acids include amino acids having acidic, basic or hydrophilic side chains and nonpolar amino acids include amino acids having aromatic or hydrophobic side chains.
  • Nonpolar amino acids may be further subdivided to include, among others, aliphatic amino acids.
  • the definitions ofthe classes of amino acids as used herein are as follows:
  • Nonpolar Amino Acid refers to an amino acid having a side chain that is uncharged at physiological pH, that is not polar and that is generally repelled by aqueous solution.
  • Examples of genetically encoded hydrophobic amino acids include Ala, He, Leu, Met, Trp, Tyr and Nal.
  • Examples of non-genetically encoded nonpolar amino acids include t-BuA, Cha and ⁇ le.
  • Aromatic Amino Acid refers to a nonpolar amino acid having a side chain containing at least one ring having a conjugated ⁇ -electron system (aromatic group).
  • aromatic group may be further substituted with substituent groups such as alkyl, alkenyl, alkynyl, hydroxyl, sulfonyl, nitro and amino groups, as well as others.
  • substituent groups such as alkyl, alkenyl, alkynyl, hydroxyl, sulfonyl, nitro and amino groups, as well as others. Examples of genetically encoded aromatic amino acids mclude phenylalanine, tyrosine and tryptophan.
  • Non-genetically encoded aromatic amino acids include phenylglycine, 2-naphthylalanine, /3-2-thienylalanine, 1,2,3,4- tetrahydroisoquinoline-3-carboxylic acid, 4-chlorophenylalanine, 2- fluorophenylalanine, 3-fluorophenylalanine and 4-fluorophenylalanine.
  • Aliphatic Amino Acid refers to a nonpolar amino acid having a saturated or unsaturated straight chain, branched or cyclic hydrocarbon side chain.
  • Examples of genetically encoded aliphatic amino acids include Ala, Leu, Nal and He.
  • Examples of non-encoded aliphatic amino acids include ⁇ le.
  • Polar Amino Acid refers to a hydrophilic amino acid having a side chain that is charged or uncharged at physiological pH and that has a bond in which the pair of electrons shared in common by two atoms is held more closely by one ofthe atoms.
  • Polar amino acids are generally hydrophilic, meaning that they have an amino acid having a side chain that is attracted by aqueous solution. Examples of genetically encoded polar amino acids include asparagine, cysteine, glutamine, lysine and serine. Examples of non-genetically encoded polar amino acids include citrulline, homocysteine, N-acetyl lysine and methionine sulfoxide.
  • Acidic Amino Acid refers to a hydrophilic amino acid having a side chain pK value of less than 7. Acidic amino acids typically have negatively charged side chains at physiological pH due to loss of a hydrogen ion. Examples of genetically encoded acidic amino acids include aspartic acid (aspartate) and glutamic acid (glutamate).
  • Basic Amino Acid refers to a hydrophilic amino acid having a side chain pK value of greater than 7.
  • Basic amino acids typically have positively charged side chains at physiological pH due to association with hydronium ion.
  • genetically encoded basic amino acids include arginine, lysine and histidine.
  • non-genetically encoded basic amino acids include the non-cyclic amino acids ornithine, 2,3-diaminopropionic acid, 2,4-diaminobutyric acid and homoarginine.
  • Ionizable Amino Acid refers to an amino acid that can be charged at a physiological pH.
  • Such ionizable amino acids include acidic and basic amino acids, for example, D-aspartic acid, D-glutamic acid, D-histidine, D-arginine, D- lysine, D-hydroxylysine, D-ornithine, L-aspartic acid, L-glutamic acid, L- histidine, L-arginine, L-lysine, L-hydroxylysine or L-ornithine.
  • the above classifications are not absolute.
  • Several amino acids exhibit more than one characteristic property, and can therefore be included in more than one category.
  • tyrosine has both a nonpolar aromatic ring and a polar hydroxyl group.
  • tyrosine has several characteristics that could be described as nonpolar, aromatic and polar. However, the nonpolar ring is dominant and so tyrosine is generally considered to be nonpolar. Similarly, in addition to being able to form disulfide linkages, cysteine also has nonpolar character. Thus, while not strictly classified as a hydrophobic or nonpolar amino acid, in many instances cysteine can be used to confer hydrophobicity or nonpolarity to a peptide.
  • polar amino acids contemplated by the present invention include, for example, arginine, asparagine, aspartic acid, cysteine, glutamic acid, glutamine, histidine, homocysteine, lysine, hydroxylysine, ornithine, serine, threonine, the corresponding /3-amino acids, and structurally related amino acids, hi one embodiment the polar amino is an ionizable amino acid such as arginine, aspartic acid, glutamic acid, histidine, hydroxylysine, lysine, or ornithine.
  • nonpolar or nonpolar amino acid residues examples include, for example, alanine, valine, leucine, methionine, isoleucine, phenylalanine, tryptophan, tyrosine and the like.
  • the amino acid sequence of a peptide can be modified so as to result in a peptide variant that includes the substitution of at least one amino acid residue in the peptide for another amino acid residue, including substitutions that utilize the D rather than L form.
  • One or more ofthe residues ofthe peptide can be exchanged for another, to alter, enhance or preserve the biological activity ofthe peptide.
  • Such a variant can have, for example, at least about 10% ofthe biological activity ofthe corresponding non-variant peptide.
  • Conservative amino acid substitutions are often utilized, i.e., substitutions of amino acids with similar chemical and physical properties, as described above.
  • conservative amino acids substitutions involve exchanging aspartic acid for glutamic acid; exchanging lysine for arginine or histidine; exchanging one nonpolar amino acid (alanine, isoleucine, leucine, methionine, phenylalanine, tryptophan, tyrosine, valine) for another; and exchanging one polar amino acid (aspartic acid, asparagine, glutamic acid, glutamine, glycine, serine, threonine, etc.) for another.
  • the variants are screened for biological activity.
  • the cyclic peptides ofthe invention can have an amino acid sequence having formula I:
  • m is an integer ranging from 1 to 7; each p is separately an integer ranging from 0 to 7; each Xi, X 2 , X 3 , X 4 , X 5 , X 6 , X , X 8 , Xg, and X ⁇ 0 is separately a' polar D- or L- ⁇ -amino acid; and each Yi, Y 2 , Y 3 , Y 4 , Y 5 , Y 6 , Y 7 , Y 8 , Y 9 , and Y 10 is separately nonpolar D- or L- ⁇ -amino acid; and wherein the cyclic peptide has an even number of from four to about sixteen alternating D- and L- ⁇ amino acids.
  • the cyclic peptides ofthe invention can have an amino acid sequence having formula II:
  • m is an integer ranging from 1 to 7; each p is separately an integer ranging from 0 to 7; each Xi, X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , and X 8 is separately a polar D- or
  • each Yi, Y 2 , Y 3 , Y 4 , Y 5 , Y 6 , Y 7 , and Y 8 is separately nonpolar D- or L- ⁇ -amino acid; and wherein the cyclic peptide has an even number of from four to about sixteen alternating D- and L- ⁇ amino acids.
  • the cyclic peptides ofthe invention can have an amino acid sequence having formula III:
  • m is an integer ranging from 1 to 7; each p is separately an integer ranging from 0 to 7; each Xi, X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , X 8 , X 9 , and X10 is separately a polar D- or L- ⁇ -amino acid; each Yi, Y 2 , Y_, Y 4 , Y 5 , Y 6 , Y7, Ys, Y9, and Y10 is separately nonpolar D- or L- ⁇ -amino acid; and wherein the cyclic peptide has an even number of from four to about sixteen alternating D- and L- ⁇ amino acids.
  • the cyclic peptide has an amino acid sequence of formula IVa or INb:
  • n is an integer ranging from 0 to 4;
  • m is an integer ranging from 1 to 7;
  • Xi, X 2 and X 3 are each a separate a polar amino acid; Yi, Y 2 and Y 3 are each a separate nonpolar amino acid; and wherein the cyclic peptide has an even number of from four to about sixteen alternating D- and L- ⁇ amino acids.
  • the cyclic peptide has an amino acid sequence of formula Na or Na:
  • Va Vb wherein: q is an integer ranging from 2 to 7;
  • Xi and X 2 are separately polar amino acids
  • Yi and Y 2 are separately nonpolar amino acids.
  • the claimed cyclic peptides ofthe above formulae exclude those composed entirely of nonpolar amino acids.
  • a peptide having any one ofthe following sequences may be excluded from one or more ofthe above formulae: cyclo-[-(Gln- D-Ala) -] cyclo-[-(Gln- D-Leu) 4 -] cyclo-[-(Gln- D-Val) 4 -] cyclo-[-(Phe- D-Leu) -] cyclo-[-(Phe- D-Ala) 4 -] cyclo-[-(Gln- D-Ala-Glu- D-Ala) 2 -] cyclo-[-(Gln- D-Phe-Glu- D-Phe) 2 -] cyclo-[-(Gln- D-Ala-Glu- D-Ala) 3 -] cyclo-[-(T - D
  • sequences may or may not be excluded from the above formulae and associated peptides and compositions: cyclo-[-D-Arg-Gln-D-Arg-Ala- D-Trp-Leu- D-Trp-Trp-]; cyclo-[-D-Arg-Gln-D-Arg-Leu-D-Trp-Leu- D-Trp-Trp-] ; cyclo-[-D-Arg-Gln-D-Arg-Val-D-Trp-Leu- D-Trp-Trp-]; cyclo-[-D-Arg-Gln-D-Arg-Phe-D-Trp-Leu- D-Trp-Trp-]; or cyclo-[-D-Arg-Gln-D-Arg-Trp-D-Trp-Leu- D-Trp-Trp-] .
  • Cyclic peptides having any ofthe above sequences, however, including any of the excluded sequences, may be included within or excluded from pharmaceutical compositions and peptides ofthe present invention.
  • the X amino acids in the above formulae can be D-serine, D-threonine, D-asparagine, D-glutamine, D-aspartic acid, D-cysteine, D-glutamic acid, D-histidine, D-homocysteine, D-arginine, D-lysine, D-hydroxylysine, D- ornithine, L-serine, L-threonine, L-asparagine, L-glutamine, L-aspartic acid, L- cysteine, L-glutamic acid, L-histidine, L-homocysteine, L-arginine, L-lysine, L- hydroxylysine or L-ornithine, provided that the ⁇ -cyclic peptide has a sequence of alternating D- and L- ⁇ -amino acids.
  • one or more ofthe X amino acids are ionizable amino acids.
  • ionizable amino acids include, for example, D-aspartic acid, D-glutamic acid, D-histidine, D-arginine, D-lysine, D-hydroxylysine, D-oniithine, L-aspartic acid, L-glutamic acid, L-histidine, L-arginine, L-lysine, L- hydroxylysine or L-ornithine.
  • the Y amino acids in the above formulae can be, for example, L-alanine, L- valine, L-leucine, L-methiomne, L-isoleucine, L-phenylalanine, L-tryptophan, L-tyrosine, D-alanine, D-valine, D-leucine, D-methionine, D-isoleucine, D- phenylalanine, D-tyrosine or D-tryptophan, provided that the ⁇ -cyclic peptide has a sequence of alternating D- and L- ⁇ -amino acids.
  • the Y amino acids may be L-tryptophan, D-tryptophan, L-leucine or D-leucine, provided that the cyclic peptide has a sequence of alternating D- and L-amino acids.
  • the cyclic peptides ofthe present invention include any of SEQ ID NO:5, 7-22, 26-29, 40, 41, 43-55, 57, 58, 61-67, 72-77, 79-89, 91-93, 97-102, 107, 109-112, 114-117, 119-122, 125, 126, 128, 129, 133, 139, 140 or 141.
  • the cyclic peptides employed are those with SEQ ID NO:8, 9, 12, 17, 18, 26, 29, 47-52, 61, 63, 67, 68, 72-77, 84, 85, 87-89, 91-93, 100, 102, 107, 111, 112, 119, 125 and 139.
  • Formulations or compositions containing the present cyclic peptides can include a mixture of two or more cyclic peptides.
  • the present isolated, purified peptides or variants thereof can be synthesized in vitro, e.g., by the solid phase peptide synthetic method or by enzyme catalyzed peptide synthesis or with the aid of recombinant DNA technology.
  • Solid phase peptide synthetic method is an established and widely used method, which is described in references such as the following: Stewart et al., Solid Phase Peptide Synthesis. W. H. Freeman Co., San Francisco (1969); Merrifield, J. Am. Chem. Soc. 85_ 2149 (1963); Meienhofer in "Hormonal
  • peptides can be further purified by fractionation on immunoaffinity or ion-exchange columns; ethanol precipitation; reverse phase HPLC; chromatography on silica or on an anion- exchange resin such as DEAE; chromatofocusing; SDS-PAGE; ammonium sulfate precipitation; gel filtration using, for example, Sephadex G-75; ligand affinity chromatography; or crystallization or precipitation from non-polar solvent or nonpolar/polar solvent mixtures. Purification by crystallization or precipitation is preferred.
  • libraries of peptides can be made using a one-bead-one-compound strategy provided by Lam et al. (97 Chem. Rev. 411-448 (1997) or synthesized on macrobeads by a split and pool method of Furka, et al. (37 Int. J. Pept. Prot. Res. 487-493(1991)).
  • Mass spectrometric sequence analysis techniques enable rapid identification of every peptide within a given library. See, Biemann, K. 193 Methods Enzymol. 455 (1990).
  • synthetic operations including peptide cyclization, are performed on solid support to avoid laborious and difficult to automate solution-phase operations.
  • the final product of the synthesis regimen is generally sufficiently pure for biological assays without laborious purification procedures. Peptide yields from each synthesis can be sufficient for performing 50 to 100 assays. Rapid, automatic mass-spectrometry- based peptide sequence analysis can be performed to identify peptide sequences that have high activity and to discard peptide sequences with low activity.
  • the synthetic approach employed can provide individually separable and identifiable peptide sequences to avoid the use of combinatorial library mixtures and laborious deconvolution techniques.
  • libraries of impure mixtures of peptides can also be generated for testing.
  • Impure preparations of peptides can be used for quick screening of combinations of sequences. When a mixture of peptides shows activity, the peptides in the mixture can either be individually isolated and tested or pure peptides having sequences known to be present in the impure mixture can be individually prepared and tested.
  • Salts of carboxyl groups of a peptide or peptide variant of the invention may be prepared in the usual manner by contacting the peptide with one or more equivalents of a desired base such as, for example, a metallic hydroxide base, e.g., sodium hydroxide; a metal carbonate or bicarbonate base such as, for example, sodium carbonate or sodium bicarbonate; or an amine base such as, for example, triethylamine, triethanolamine, and the like.
  • a desired base such as, for example, a metallic hydroxide base, e.g., sodium hydroxide
  • a metal carbonate or bicarbonate base such as, for example, sodium carbonate or sodium bicarbonate
  • an amine base such as, for example, triethylamine, triethanolamine, and the like.
  • N-acyl derivatives of an amino group ofthe peptide or peptide variants may be prepared by utilizing an N-acyl protected amino acid for the final condensation, or by acylating a protected or unprotected peptide.
  • O-acyl derivatives may be prepared, for example, by acylation of a free hydroxy peptide or peptide resin. Either acylation may be carried out using standard acylating reagents such as acyl halides, anhydrides, acyl imidazoles, and the like. Both N- acylation and O-acylation may be carried out together, if desired.
  • Acid addition salts ofthe peptide or variant peptide, or of amino residues ofthe peptide or variant peptide may be prepared by contacting the peptide or amine with one or more equivalents ofthe desired inorganic or organic acid, such as, for example, hydrochloric acid.
  • Esters of carboxyl groups ofthe peptides may also be prepared by any ofthe usual methods known in the art.
  • the invention also contemplates cyclic peptides composed of one or more ⁇ amino acids. Such /3-amino acids can be substituted along their peptide backbones by one to two substituents.
  • Such substituents can include cycloalkyl, cycloalkenyl, and heterocylic rings that encompass the ⁇ and ⁇ carbons ofthe ⁇ - peptide backbone. These rings can be, for example, C 3 -C 8 cycloalkyl, cycloalkenyl or heterocyclic rings having one or more nitrogen atoms as the sole heteroatom, and can be substituted or unsubstituted.
  • the substituents on the ring or on the ⁇ and ⁇ carbons ofthe /3-peptide can be, for example, hydroxy, linear or branched C ⁇ -C 6 -alkyl, alkenyl, alkynyl; hydroxy-C ⁇ -C 6 -alkyl; amino-C ⁇ -C 6 - alkyl; C ⁇ -C 6 -alkyloxy, C ⁇ -C 6 -alkoxy-alkyl; C ⁇ -C 6 - amino; mono- or di-C ⁇ -C 6 - alkylamino; carboxamido; carboxamido-C ⁇ -C 6 -alkyl; sulfonamido; sulfonamido- C ⁇ -C 6 -alkyl, urea, cyano, fluoro, thio; C_-C 6 -alkylthio; mono- or bicyclic aryl; mono- or bicyclic heteroaryl having up to 5 heteroatoms selected from N, O
  • the cyclic ⁇ -peptides ofthe invention can have an amino acid sequence of formula VI: r- (Z P -(Z 2 ) p -(Z 3 ) p -(Z 4 ) p -(Z 5 ) p -(Z 6 ) p -(Z 7 ) p -(Z 8 ) p -(Z 9 ) p -(Z 10 )p
  • each p is separately an integer ranging from 0 to 7; each Zi, Z 3 , Z 5 , Z 7 , Z 9 , Zn, Z ⁇ 3 , Z ⁇ 5 , Z ⁇ 7 , and Z ⁇ 9 is separately a monosubstituted ⁇ -amino acid; each Z 2 , Z 4 , Z 6 , Z 8 , Zio, Z J , Z ⁇ 4 , Z ⁇ 6 , Z ⁇ 8 , and Z 2 o is separately a disubstituted ⁇ -amino acid; and wherein the cyclic ⁇ -peptide has a sequence of from three to about ten homochiral ⁇ -amino acids.
  • the cyclic peptides provided herein are believed self-assemble into supramolecular structures.
  • Self-assembly means that a collection of cyclic peptides can associate to form a supramolecular structure on or within a cellular membrane without the assistance of anything other than the components ofthe cellular membrane.
  • the physical and chemical properties ofthe cellular membrane facilitate self-assembly ofthe cyclic peptides.
  • the interaction between the components of microbial cellular membranes and the cyclic peptides determines whether the cyclic peptides are selective for those cellular membranes.
  • supramolecular structures by the peptides ofthe invention is supported by high-resolution imaging using cryo-electron microscopy, electron diffraction, Fourier-transform infrared spectroscopy, and molecular modeling. Supramolecular structures have been further characterized by IR spectroscopy, low-dose electron microscopy, and the analysis of electron diffraction patterns.
  • cyclic peptide structures that are made up of an even number of alternating D- and L-amino acid residues are believed to adopt or sample a flat ring-shaped conformation in which all backbone amide functionalities lie approximately perpendicular to the plane of the ring structure.
  • cyclic peptides made up of /3-amino acids can also adopt a flat-ring structure, hi this flat-ring conformation, it is believed that the peptide subunits can stack, under favorable conditions, to furnish a contiguous hydrogen bonded hollow tubular structure that is referred to herein as a nanotube (see Figures 1 and 7).
  • a nanotube for example, controlled acidification of alkaline solutions of peptide
  • SEQ ID NO:l (cyclo[-(Gln-D-Ala-Glu D-Ala) 3 -]) yielded rod shaped crystalline materials that appeared under transmission electron microscopy as organized bundles of tightly packed tubular structures.
  • Low dose cryo microscopy according to the method of M. Adrian et al. (308 Nature 32-36 (1984)) and of R.A. Milligan et al. (13 Ultramicroscopy 1-10 (1984)) revealed longitudinal striations with spacing of approximately 25 A as expected for the center to center spacing for closely packed tubular structures.
  • Electron diffraction patterns display axial spacing of 4.80 A that is in agreement with the peptide stacking and the formation of tight network of hydrogen bonded b-sheet type structure.
  • the meridonial spacing in the electron diffraction patterns display spacing of
  • the model shows structure factors similar to the patterns observed in the electron diffraction thus supporting the proposed three- dimensional model.
  • Involvement of intermolecular hydrogen bonding network in a tube-like assembly is also supported by FT-IR spectroscopic analysis according to the method of S. Krimm et al. (Advances in Protein Chemistry; Anfinsen, C. B., Edsall, J. T.; Richards, F.
  • Nanotubes display characteristic IR features of a / 8-sheet structure signified not only by the amide /bands at 1626 cm “1 and 1674 cm “1 and an amide //band at 1526 cm “1 , but also by the observed NH stretching frequency at 3291 cm "1 supporting formation of a tight network of hydrogen bonds.
  • IR spectrum is similar to tubular structures that have been discovered in nature.
  • nanotubular structures for some ofthe present peptides can be conceptually related to the structure of crystalline linear Gramicidin A that is known to form dimeric /3-helical structures.
  • Gramicidin A has amide I bands at 1630, 1685 cm “1 , an amide //band at 1539 cm “1 , and an NH stretching frequency at 3285 cm “1 .
  • the observed frequency of NH stretching mode correlates to an average mtersubunit distance of 4.76 A that is in close agreement with the value of 4.80 A obtained independently from the electron diffraction patterns.
  • the pore size, or internal diameter, of self-assembled nanotubes can be adjusted by the ring size ofthe peptide subunit employed.
  • a twelve-residue cyclic peptide structure for example cyclo[-(Gln-D-Ala-Glu-D-Ala) -] (SEQ ID NO:l), has a diameter of about 13 A.
  • the eight residue cyclic peptide cyclo[- (Trp-D-Leu) 3 -Gln-D-Leu-] (SEQ ID NO:2) has a diameter of approximately 7.5 A in diameter.
  • a cyclic peptide having SEQ ID NO:2 in synthetic phosphatidylcholine liposomes displays an FTIR m/cfe-Zband at 1624 cm “1 and an observed N-H stretching frequency at 3272 cm “1 that support formation of a tight network of ⁇ -sheet-like hydrogen bonds with an average intersubunit distance of 4.7 A to 4.8 A.
  • the flat, ring-shaped cyclic peptides ofthe present invention are not only structurally predisposed toward intermolecular interaction, but are also energetically favored to self-assemble on selected microbial cell membranes and permeabilize cells through formation of pores or other membrane destabilizing structures.
  • Unilamellar vesicles were prepared by the reverse-phase evaporation using DPPC, OPPC, cholesterol in the ratio of 1:1:2 in a solution containing 5(6)-carboxyfluorescem (20 mM in phosphate/saline buffer: 137 mM NaCl, 2.6 mM KCI, 6.4 mM Na 2 HPO 4 , 1.4 mM KH 2 PO 4 , pH 6.5) according to the method of F. Szoka et al. in Proc. Natl. Acad. Sci. USA (1978), vol. 75, pages 4194- 4198.
  • Liposomes were then sized by multiple extrusions through Nucleopore® polycarbonate membranes (10 times, 50 psi, using 0.8 and 2x0.4 micron filter stacks) and the untrapped 5(6)-carboxyfluorescein was removed by size exclusion chromatography (Sephadex G-25 column 1x30 cm) using the same phosphate/saline buffer according to the method of F. Olson et al. in Biochim. Biophys. Acta (1979), vol. 557, pages 9-23. Vesicles formed in this way are approximately 150 nanometer in diameter as determined by electron microscopy. (R.R.C. New, Ed. Liposomes, Oxford university Press, 1990).
  • the ring structure of this peptide is N- methylated on one face. Such N-methylation does not adversely affect the ability of the peptide to interact with liposomal membranes but predisposes peptides toward a dimeric cylindrical structure that cannot span a normal liposomal membrane.
  • the peptide has been shown to partition effectively into liposomes, it does not promote proton transport activity in the above vesicle experiments. Together, these experiments support the idea that not only are the side chains displayed on cyclic peptides important for membrane interaction, but also the peptide backbone should be able to participate in extended intermolecular hydrogen bonding, for example, to facilitate membrane permeabilization.
  • the present invention is directed to methods of treating or preventing or otherwise ameliorating microbial infections in a mammal, as well as other animals, such as farm animals and birds. These methods include administering to the animal an effective amount, for example, a therapeutically effective amount of a cyclic peptide ofthe present invention.
  • Treatment of, or treating, microbial infections is intended to include the alleviation of or diminishment of at least one symptom typically associated with the infection.
  • the treatment also includes alleviation or diminishment of more than one symptom.
  • the treatment cures, e.g., substantially kills the microbes and/or eliminates the symptoms associated with the infection.
  • Microbial infections that can be treated by the present cyclic peptides include infections by any target microbial organisms that can infect a mammal or other animal.
  • target microbial organisms include essentially any single cell organism or parasite that has a cellular membrane and that can infect an animal, including mammals.
  • target microbial organisms include bacteria, fungi, yeast strains and other single cell organisms.
  • Cyclic peptides are active against both gram-negative and gram-positive bacteria. Hence, for example, infections or unwanted levels ofthe following target microbial organisms can be treated, prevented or addressed by the present cyclic peptides: Aeromonas spp.
  • Bacillus spp. including, for example, Bacillus cereus, Bacillus anthracis and Bacillus thuringiensis
  • Bacteroides spp. including, for example, B.fragilis, B. thetaiotaomicron, B. vulgatus, B. ovatus, B. distasonis, B. uniformis, B. stercoris, B. eggerthii, B. merdae, and R. caccae
  • Clostridium spp. such as the pathogenic clostridia including all types of Clostridium botulinum (including those in Groups I, II, III and IN, and including those that produce botulism A, B, C, D, E, F and G), all types of Clostridium tetani, all types of Clostridium difficile, and all types of Clostridium perfringens), Enterobacter spp.
  • Enterobacter aerogenes also sometimes referred to as Klebsiella mobilis
  • Enterobacter agglomerans also sometimes referred to as Pantoea agglomerans
  • Enterobacter amnigenus Enterobacter asburiae
  • Enterobacter cancerogenus also sometimes referred to as Enterobacter taylorae and/or Erwinia cancerogena
  • Enterobacter cloacae Enterobacter cowanii
  • Enterobacter dissolvens also sometimes referred to as Erwinia dissolvens
  • Enterobacter gergoviae Enterobacter hormaechei
  • Enterobacter intermedium Enterobacter intermedius
  • Enterobacter kobei Enterobacter nimipressuralis
  • Enterobacter sakazakii Enterobacter taylorae
  • VRE Vancomycin Resistant Enterococcus
  • ETEC enterotoxigenic
  • EPEC enteropathogenic
  • EHEC enterohemorrhagic
  • EIEC enteroinvasive
  • Helicobacter spp. including, for example, Gastrospirillum hominis (also sometimes now referred to as Helicobacter heilmannii), Helicobacter spp. (including, for example, Helicobacter pylori and Helicobacter hepaticus), Klebsiella spp. (including, for example, Klebsiella pneumoniae, Klebsiella ozaenae, Klebsiella rhinos cleromatis, Klebsiella oxytoca, Klebsiella planticola, Klebsiella terrigena, and Klebsiella ornithinolytica), Salmonella spp. (including, for example, S. typhi and S. paratypl ⁇ A, B, and C, S.
  • Shigella spp. including, for example, Shigella sonnei, Shigella boydii, Shigella flexneri, and Shigella dysenteriae
  • Staphylococcus spp. including, for example, Staphylococcus aureus, methicillin-resistant Staphylococcus aureus (MRSA), Staphylococcus saprophyticus and Staphylococcus epidermis
  • Streptococcus ssp including, for example, Shigella sonnei, Shigella boydii, Shigella flexneri, and Shigella dysenteriae
  • Staphylococcus spp. including, for example, Staphylococcus aureus, methicillin-resistant Staphylococcus aureus (MRSA), Staphylococcus saprophyticus and Staphylococcus epidermis
  • Streptococcus ssp including, for example, Staphylococcus aureus, meth
  • Streptococcus pyogenes including Groups A (one species with 40 antigenic types, Streptococcus pyogenes), B, C, D (five species (Streptococcus faecalis, Streptococcus faecium, Streptococcus durans, Streptococcus avium, and Streptococcus bovis)), F, and G, including Streptococcus pneumoniae), Pseudomonas spp.
  • Vibrio cholera Serogroup OI and Vibrio cholera Serogroup Non-Ol Vibrio par ahaemolyticus, Vibrio alginolyticus, Vibrio furnissii, Vibrio carchariae, Vibrio hollisae, Vibrio multiplinnatiensis, Vibrio metschnikovii, Vibrio damsela, Vibrio mimicus, Vibrio vulnificus, and Vibrio fluvialis
  • Yersinia spp including, for example, Vibrio cholera Serogroup OI and Vibrio cholera Serogroup Non-Ol, Vibrio par ahaemolyticus, Vibrio alginolyticus, Vibrio furnissii, Vibrio carchariae, Vibrio hollisae, Vibrio suffinnatiensis, Vibrio metschnikovii, Vibrio damsela, Vibrio mimicus, Vibri
  • Yersinia pestis including, for example, Yersinia pestis, Yersinia enterocolitica and Yersinia pseudotuberculosis
  • Neisseria including, for example, Yersinia pestis, Yersinia enterocolitica and Yersinia pseudotuberculosis
  • Neisseria Proteus, Citrobacter, Aerobacter
  • Providencia Serratia
  • Brucella Francisella tularensis
  • Bacillus tularensis Bacillus tularensis
  • Brucella tularensis also sometimes referred to as Pasteurella tularensis
  • Bacillus tularensis Bacillus tularensis
  • Brucella tularensis tularemia
  • rabbit fever deerfly fever
  • Ohara's disease Ohara's disease
  • Francis disease and the like.
  • various bacterial infections or unwanted levels of bacteria that can be treated, prevented or addressed by the present peptides include but are not limited to those associated with anthrax (Bacillus anthracis), staph infections (Staphylococcus aureus), typhus (Salmonella typhi), food poisoning (Escherichia coli, such as O157:H7), bascillary dysentery (Shigella dysenteria), pneumonia (Psuedomonas aerugenosa and 'or Pseudomonas cepacia), cholera (Vivrio cholerae), ulcers (Helicobacter pylori), Bacillus cereus, Salmonella, Clostridium perfringens, Campylobacter, Listeria monocytogenes, Vibrio par ahaemolyticus, botulism (Clostridium botulinum), smallpox (variola major), listeriosis (Listeria monocytogenes
  • E. coli serotype 0157:H7 has been implicated in the pathogenesis of diarrhea, hemorrhagic colitis, hemolytic uretnic syndrome (HUS) and thrombotic thrombocytopenic purpura (TTP).
  • the peptides ofthe invention are also active against drug-resistant and multiply-drug resistant strains of bacteria, for example, multiply-resistant strains o ⁇ Staphylococcus aureus and vancomycin-resistant strains o ⁇ Enterococcus faecium and Enterococcus faecalis.
  • Anti-microbial activity can be evaluated against these varieties of microbes using methods available to one of skill in the art.
  • Anti-microbial activity for example, is determined by identifying the minimum inhibitory concentration (MIC) of a cyclic peptide ofthe present invention that prevents growth of a particular microbial species.
  • anti-microbial activity is the amount ofthe peptide that kills 50% ofthe microbes when measured using standard dose or dose response methods.
  • the present invention also provides a method of evaluating therapeutically effective dosages for treating a microbial infection with cyclic peptides described and claimed herein that includes determining the minimum inhibitory concentration of a cyclic peptide at which substantially no microbes grow in vitro. Such a method permits calculation ofthe approximate amount of cyclic peptide needed per volume to inhibit microbial growth or to kill 50% of the microbes. Such amounts can be determined, for example, by standard microdilution methods. For example, a series of microbial culture tubes containing the same volume of medium and the substantially the same amount of microbes are prepared, and an aliquot of cyclic peptide is added. The aliquot contains differing amounts of cyclic peptide in the same volume of solution.
  • the microbes are cultured for a period of time corresponding to one to ten generations and the number of microbes in the culture medium is determined.
  • the optical density ofthe cultural medium can be used to estimate whether microbial growth has occurred - if no significant increase in optical density has occurred, then no significant microbial growth has occurred. However, if the optical density increases, then microbial growth has occurred.
  • a small aliquot of the culture medium can be removed at the time when the cyclic peptide is added (time zero) and then at regular intervals thereafter.
  • the present invention is also directed, for example, to methods of treating fungal infections in a mammal or other animal, which include administering to the mammal or other animal a therapeutically effective amount of a cyclic peptide ofthe present invention.
  • a cyclic peptide ofthe present invention it is believed that the cyclic peptide undergoes self-assembly to form a supramolecular structure that prevents or interrupts target fungal infections, or inactivates target fungi, but does not cause undesired toxicity or substantial hemolysis of non-infected mammalian or animal cells.
  • Treatment of, or treating, fungal infections is intended to include the alleviation of or diminishment of at least one symptom typically associated with the infection.
  • the treatment also includes alleviation or diminishment of more than one symptom.
  • the treatment may cure the infection, e.g., it may substantially inactivate the fungus and/or eliminate the symptoms associated with the infection.
  • Fungal infections that can be treated or prevented by the present cyclic peptides include infections by fungi that infect a mammal, including Histoplasma capsulatum, Coccidioides immitis, Cryptococcus neoformans, Candida ssp. including Candida albicans, Aspergilli ssp. including Aspergillus fumigatus, Sporothrix, Trichophyton ssp., Fusarium ssp., Tricosporon ssp., Pneumocystis carinii, and Trichophyton mentagrophytes.
  • infections or unwanted levels of target fungi can be treated, prevented or addressed by the present cyclic peptides.
  • Such fungi also include fungal pathogens that may have potential for use biological weapons, including Coccidioides immitis and Histoplasma capsulatum.
  • the cyclic peptides provided herein do not cause substantial or undesired toxicity against mammalian cells or the cells of other animals to be treated.
  • Mammalian or bird red blood cell hemolysis is one way to measure whether a cyclic peptide can cause undesired toxicity against mammalian cells or the cells of other animals to be treated. If a cyclic peptide can self-assemble by association with a mammalian or animal cell membrane, the membrane may be disrupted. Red blood cells are conveniently used to test for membrane disruption, because they undergo hemolysis, which can be detected as the release of hemoglobin from the cell. Hemolysis assays can be performed by methods available to one of skill in the art.
  • hemoglobin after exposure to test compounds, the release of hemoglobin can be observed spectrophotometrically by observing the absorbance of light at wavelengths characteristic of hemoglobin, for example, at 543 nm.
  • Control samples can be used, for example, the medium in which the cells are tested or maintained can serve as a zero blank.
  • a second control can be used to determine the absorbance value for 100% lysis or hemolysis that can be a sample that is identical to the test mammalian cell sample but which had been sonicated to completely disrupt the cells.
  • hemolytic agents such as mellitin or a variety of detergents can also be used to establish 100% hemolysis of test red blood cells.
  • Screening Assays Screening or other assays may be used to identify, confirm or evaluate cyclic peptides that can selectively interact with, rupture of kill a microbe or other cell type of interest.
  • a wide variety of assays may be used for this purpose. H general, such an assay can involve contacting a microbe or other cell type of interest with at least one cyclic peptide and observing whether the cyclic peptide interacts with a microbe or other cell type of interest and/or has deleterious effects upon that microbe or other cell type.
  • cyclic peptides ofthe invention can be labeled with a reporter molecule that permits detection ofthe peptide. After labeling, the cyclic peptides can be contacted with the cell type of interest for a time and under conditions that permit binding or association ofthe peptide to cellular membranes. The cells can be washed with physiological solutions to remove unbound or unassociated cyclic peptides, and the microbes or cells can then be observed to ascertain whether the reporter molecule is bound or associated with the microbes, cells or cellular membranes.
  • one of skill in the art can test whether the cyclic peptide(s) can selectively penetrate the membranes of particular microbes or other selected cell types. This may be done, for example, by examining whether the reporter molecule remains associated with the cellular membranes ofthe microbe or cell type of interest or whether the reporter molecule becomes associated with the interior ofthe microbe or cell type of interest.
  • Reporter molecules that can be employed include any detectable compound or molecule available to one of skill in the art that is conjugated directly or indirectly to a cyclic peptide ofthe invention.
  • the label may itself be detectable (e.g., radioisotope labels or fluorescent labels) or, in the case of an enzymatic label, may catalyze chemical alteration of a substrate compound or composition that is detectable or molecular epitopes for protein/antibody capture and detection.
  • Deleterious effects upon the microbe or cell type of interest can also be detected as an indication of an interaction between a cyclic peptide ofthe invention and the microbe or cell type of interest. Such deleterious effects may be confirmed by any evidence that the cyclic peptide has had an adverse or cytotoxic effect upon the microbe or cell type of interest. For example, one of skill in the art can test whether the cyclic peptide(s) kill the cell type, or cause membrane depolarization or penneabilization ofthe membranes ofthe microbes or cell types of interest.
  • cyclic peptides that have low toxicity for normal human or other animal cells but that have good antimicrobial properties (depolarizing or permeabilizing microbial cell membranes, lysing or otherwise killing microbes).
  • Such cyclic peptides may or may not interact with normal human or other animal cells so long as they have few toxic effects on such normal human or other animal cells.
  • a plurality of assays are performed in parallel with different cyclic peptides, which may be introduced at different concentrations to obtain a differential response to the various concentrations.
  • at least one control assay is included in the testing.
  • Such a control can be a negative control involving exposure ofthe microbes or cells of interest to a physiologic solution containing no cyclic peptide.
  • Another control can involve exposure ofthe microbe or cell type of interest to a cyclic peptide that has already been observed to adversely affect the microbe or cell type of interest, or a second cell type that is related to the microbe or cell type of interest.
  • Another control can involve exposing a microbe or cell type of interest to a known therapeutic agent that has a desired affect on the microbe or cell type of interest, for example, an anti-microbial or cytotoxic agent with known efficacy at a particular concentration or dosage.
  • a known therapeutic agent for example, an anti-microbial or cytotoxic agent with known efficacy at a particular concentration or dosage.
  • One of skill in the art can readily select control compounds and conditions that facilitate such evaluations.
  • cyclic peptides are obtained from a wide variety of sources including libraries of cyclic peptides generated as described herein. Cyclic peptides can also be individually or rationally designed and synthesized to have specific structural features selected by one of skill in the art.
  • any cell type available to one of skill in the art can be screened by these methods.
  • any microbial or mammalian or animal cell type can be screened to assess whether the cyclic peptides ofthe invention can selectively or non-selectively interact therewith.
  • Such microbial cell types include any single cell organism that is capable of autonomous replication. Examples include any bacterial, fungal and yeast cell types.
  • Mammalian or other animal cell types can also be screened to ascertain whether the peptides ofthe invention interact therewith and/or to determine or confirm whether the peptides ofthe invention do not interact, bind, lyse, kill or otherwise adversely affect the viability ofthe mammalian or other animal cell type of interest.
  • mammalian red blood cells are screened with the cyclic peptides to ascertain whether the cyclic peptides have an adverse effect on the red blood cells.
  • the membranes of red blood cells tend to be more sensitive to lysis than many other mammalian cell types.
  • red blood cells are a useful cell type for quickly screening whether a cyclic peptide would be expected to have any adverse effects on these or other mammalian cell types.
  • Methods of screening for mammalian cell lysis are available in the art. For example, using procedures described herein, red blood cells can be tested to ascertain whether hemolysis has occurred upon exposure to at least one cyclic peptide ofthe invention. When it is established that a cyclic peptide causes little or no undesired hemolysis of red blood cells, it may be tested against other mammalian cell types or used for in vivo testing in standard animal models.
  • Conditions for screening cyclic peptides include conditions that are used by one of skill in the art to grow, maintain or otherwise culture cell types of interest. Cell types of interest should be assayed under conditions where they would be healthy but for the presence ofthe cyclic peptide(s). Controls can be performed where the cell types are maintained under the selected culture conditions and not exposed to a cyclic peptide, to assess whether the culture conditions influenced the viability ofthe cells.
  • One of skill in the art can also perform the assay on cells that have been washed in simple physiological solutions, such as buffered saline, to eliminate, or test for, any interaction between the cyclic peptides or cells and the components in the culture media.
  • culture conditions for the assays generally include providing the cells with the appropriate concentration of nutrients, physiological salts, buffers and other components typically used to culture or maintain cells ofthe selected type.
  • a variety of other reagents may be included in the screening assay. These mclude reagents like salts, neutral proteins, albumin,and serum (e.g. fetal calf serum) that are used to mimic the physiologic state ofthe cell types of interest.
  • reagents like salts, neutral proteins, albumin,and serum (e.g. fetal calf serum) that are used to mimic the physiologic state ofthe cell types of interest.
  • Conditions and media for culturing, growing and maintaining mammalian cells and bacterial or other microbial cells are available to one of skill in the art.
  • the selected reagents and components are added to the assay in the order selected by one of skill in the art.
  • the cyclic peptides are added last to start the assay.
  • Assays are performed at any suitable temperature, typically between 4 °C and 40° C. Temperatures generally range from about room temperature (about 20 °C) to about 37°C. Incubation periods are selected to ascertain the optimal range of activity or to insure that the cyclic peptides do not adversely affect unwanted cell types. However, incubation times can be optimized to facilitate rapid high-throughput screening. Typically incubation times are between about 1 minute and about 24 hours, other times range from about 5 minutes to about 8 hours.
  • Cyclic peptides having the desired selectivity and activity during in vitro screening or evaluation may be tested for activity and/or lack of toxicity in vivo in an appropriate animal model.
  • animal models include mice, rats, rabbits, cats, dogs, pigs, goats, cattle or horses.
  • the mouse and the rat are convenient animal models for testing whether cyclic peptides ofthe invention have toxic effects and/or to determine whether the cyclic peptides can combat a microbial infection.
  • cyclic peptides ofthe invention can readily perform in vivo screening ofthe cyclic peptides ofthe invention.
  • a series of cyclic peptides at different test dosages can be separately administered to different animals.
  • a single dose or a series of dosages can be administered to the animal.
  • a test period is selected that permits assessment ofthe effects ofthe peptide(s) on the animal. Such a test period may run from about one day to about several weeks or months.
  • the effect of a cyclic peptide(s) on an animal can be determined by observing whether the peptide adversely affects the behavior (e.g., lethargy, hyperactivity) and physiological state ofthe animal over the course of test period.
  • the physiological state ofthe animal can be assessed by standard procedures. For example, during the test period one of skill in the art can draw blood and collect other bodily fluids to test, for example, for various enzymes, proteins, metabolites, and the like.
  • One of skill in the art can also observe whether the animal has bloating, loss of appetite, diarrhea, vomiting, blood in the urine, loss of consciousness, and a variety of other physiological problems.
  • the animal can be sacrificed and anatomical, pathological, histological and other studies can be performed on the tissues or organs ofthe animal.
  • mice or other test animals are infected with the selected microbe and a selected test dosage of one or more cyclic peptides is administered thereafter at predetermined elapsed time periods or intervals.
  • Test animals are observed over the course of several days to weeks to ascertain whether the cyclic peptide protects the animals from the microbial infection.
  • the test animals can be sacrificed and examined to ascertain whether the cyclic peptide has optimally protected the test animals from infection and/or to determine whether any adverse side effects have occurred.
  • the microbe Prior to administration, the microbe can be washed in simple physiological solutions to remove toxins or other components that may adversely affect the mice.
  • microbial cells can be grown at 37 °C with agitation for 12 hours to a stationary phase. Microbial cells can be collected by centrifugation, washed twice with saline or phosphate buffered saline (PBS) and resuspended or diluted to a convenient cell density, for example, a cell density of about of about 3-5xl0 7 cfu/ml.
  • PBS phosphate buffered saline
  • Several animals to be tested with varying amounts of each peptide five are infected with a small volume ofthe microbe (e.g. about 0.1 to about 1 ml).
  • Infection can be performed orally, intraperitoneally, intravenously or by some other route selected by one of skill in the art. After infection, the animals are allowed to rest for a short time and then each animal is treated with a different dose of peptide. The animals are monitored for several days to weeks.
  • Controls are used to establish the effects ofthe microbe when the cyclic peptide is not administered. Other controls can also be performed, for example, the safety and efficacy ofthe present cyclic peptides can be compared to that of known anti-microbial agents (e.g., penicillin, kanamycin, vancomycin, erythromycin, etc.).
  • known anti-microbial agents e.g., penicillin, kanamycin, vancomycin, erythromycin, etc.
  • the invention further provides a method of identifying or evaluating a D-, L- ⁇ -cyclic peptide or a ⁇ -peptide capable of selective association with a target biomolecule.
  • target biomolecules can include, for example, intracellular, extracellular or membrane-associated proteins, enzymes, nucleic acids, receptors, organelles and the like. This method can involve contacting a solution of cyclic peptides with the target biomolecule under hydrogen bond-promoting conditions and determining whether the peptides selectively associate with the desired biomolecules and possess biological activity of interest.
  • the target biomolecule can be displayed, for example, on the surface of a living cell, on the surface of a genetically engineered cell or on the surface of a liposome.
  • the peptide can be contacted with the target biomolecule under other desired assay conditions available to one of skill in the art.
  • Cyclic peptides having good anti-microbial properties in vitro and/or in vivo that also have substantially no undesired toxicity against unwanted cell types are particularly good candidates for the preparation of appropriate dosage forms, as described in more detail below. Dosages, Formulations and Routes of Administration for the Peptides
  • the peptides ofthe invention are administered so as to achieve a reduction in at least one symptom associated with an infection, indication or disease, or a decrease in the amount of antibody associated with the indication or disease.
  • the peptide, a variant thereof or a combination thereof may be administered as single or divided dosages, for example, of at least about 0.01 mg/kg to about 500 to 750 mg/kg, of at least about 0.01 mg/kg to about 300 to 500 mg/kg, at least about 0.1 mg/kg to about 100 to 300 mg/kg or at least about 1 mg/kg to about 50 to 100 mg/kg of body weight, although other dosages may provide beneficial results.
  • the amount admimstered will vary depending on various factors including, but not limited to, the cyclic peptide chosen, the disease, the weight, the physical condition, the health, the age ofthe mammal, whether prevention or treatment is to be achieved, and if the peptide is chemically modified. Such factors can be readily determined by the clinician employing animal models or other test systems that are available in the art.
  • Administration ofthe therapeutic agents in accordance with the present invention may be in a single dose, in multiple doses, in a continuous or intermittent manner, depending, for example, upon the recipient's physiological condition, whether the purpose ofthe administration is therapeutic or prophylactic, and other factors known to skilled practitioners.
  • the administration of the peptides of the invention may be essentially continuous over a preselected period of time or may be in a series of spaced doses. Both local and systemic administration is contemplated.
  • peptides are synthesized or otherwise obtained, purified as necessary or desired and then lyophilized and stabilized. The peptide can then be adjusted to the appropriate concentration, and optionally combined with other agents.
  • the absolute weight of a given peptide included in a unit dose can vary widely. For example, about 0.01 to about 2 g, or about 0.1 to about 500 mg, of at least one peptide ofthe invention, or a plurality of peptides specific for a particular cell type can be administered.
  • the unit dosage can vary from about 0.01 g to about 50 g, from about 0.01 g to about 35 g, from about 0.1 g to about 25 g, from about 0.5 g to about 12 g, from about 0.5 g to about 8 g, from about 0.5 g to about 4 g, or from about 0.5 g to about 2 g.
  • Daily doses ofthe cyclic peptides ofthe invention can vary as well. Such daily doses can range, for example, from about 0.1 g/day to about 50 g/day, from about 0.1 g/day to about 25 g/day, from about 0.1 g/day to about 12 g/day, from about 0.5 g/day to about 8 g/day, from about 0.5 g/day to about 4 g/day, and from about 0.5 g/day to about 2 g/day.
  • one or more suitable unit dosage forms comprising the therapeutic peptides ofthe invention can be administered by a variety of routes including oral, parenteral (including subcutaneous, intravenous, intramuscular and intraperitoneal), rectal, dermal, transdermal, intrathoracic, intrapulmonary and intranasal (respiratory) routes.
  • the therapeutic peptides may also be formulated for sustained release (for example, using microencapsulation, see WO 94/ 07529, and U.S. Patent No.4,962,091).
  • the formulations may, where appropriate, be conveniently presented in discrete unit dosage forms and may be prepared by any ofthe methods well known to the pharmaceutical arts. Such methods may include the step of mixing the therapeutic agent with liquid carriers, solid matrices, semi-solid carriers, finely divided solid carriers or combinations thereof, and then, if necessary, introducing or shaping the product into the desired delivery system.
  • the therapeutic peptides ofthe invention are prepared for oral administration, they are generally combined with a pharmaceutically acceptable carrier, diluent or excipient to form a pharmaceutical formulation, or unit dosage form.
  • a pharmaceutically acceptable carrier diluent or excipient
  • the peptides may be present as a powder, a granular formulation, a solution, a suspension, an emulsion or in a natural or synthetic polymer or resin for ingestion ofthe active ingredients from a chewing gum.
  • the active peptides may also be presented as a bolus, electuary or paste.
  • Orally administered therapeutic peptides ofthe invention can also be formulated for sustained release, e.g., the peptides can be coated, micro-encapsulated, or otherwise placed within a sustained delivery device.
  • the total active ingredients in such formulations comprise from 0.1 to 99.9% by weight ofthe formulation.
  • pharmaceutically acceptable it is meant a carrier, diluent, excipient, and/or salt that is compatible with the other ingredients ofthe formulation, and not deleterious to the recipient thereof.
  • Pharmaceutical formulations containing the therapeutic peptides ofthe invention can be prepared by procedures known in the art using well-known and readily available ingredients.
  • the peptide can be formulated with common excipients, diluents, or carriers, and formed into tablets, capsules, solutions, suspensions, powders, aerosols and the like.
  • excipients, diluents, and carriers that are suitable for such formulations include buffers, as well as fillers and extenders such as starch, cellulose, sugars, mannitol, and silicic derivatives.
  • Binding agents can also be included such as carboxymethyl cellulose, hydroxymethylcellulose, hydroxypropyl methylcellulose and other cellulose derivatives, alginates, gelatin, and polyvinyl-pyrrolidone.
  • Moisturizing agents can be included such as glycerol, disintegrating agents such as calcium carbonate and sodium bicarbonate.
  • Agents for retarding dissolution can also be included such as paraffin.
  • Resorption accelerators such as quaternary ammonium compounds can also be included.
  • Surface active agents such as cetyl alcohol and glycerol monostearate can be included.
  • Adsorptive carriers such as kaolin and bentonite can be added.
  • Lubricants such as talc, calcium and magnesium stearate, and solid polyethyl glycols can also be included. Preservatives may also be added.
  • the compositions ofthe invention can also contain thickening agents such as cellulose and/or cellulose derivatives. They may also contain gums such as xanthan, guar or carbo gum or gum arabic, or alternatively polyethylene glycols, bentones and montmorillonites, and the like.
  • tablets or caplets containing the cyclic peptides ofthe invention can include buffering agents such as calcium carbonate, magnesium oxide and magnesium carbonate.
  • Caplets and tablets can also include inactive ingredients such as cellulose, pre-gelatinized starch, silicon dioxide, hydroxy propyl methyl cellulose, magnesium stearate, microcrystalline cellulose, starch, talc, titanium dioxide, benzoic acid, citric acid, corn starch, mineral oil, polypropylene glycol, sodium phosphate, zinc stearate, and the like.
  • Hard or soft gelatin capsules containing at least one cyclic peptide ofthe invention can contain inactive ingredients such as gelatin, microcrystalline cellulose, sodium lauryl sulfate, starch, talc, and titanium dioxide, and the like, as well as liquid vehicles such as polyethylene glycols (PEGs) and vegetable oil.
  • PEGs polyethylene glycols
  • enteric-coated caplets or tablets containing one or more peptides ofthe invention are designed to resist disintegration in the stomach and dissolve in the more neutral to alkaline environment ofthe duodenum.
  • the therapeutic peptides ofthe invention can also be formulated as elixirs or solutions for convenient oral administration or as solutions appropriate for parenteral administration, for instance by intramuscular, subcutaneous, intraperitoneal or intravenous routes.
  • the pharmaceutical formulations ofthe therapeutic peptides ofthe invention can also take the form of an aqueous or anhydrous solution or dispersion, or alternatively the form of an emulsion or suspension or salve.
  • the therapeutic peptides may be formulated for parenteral administration (e.g., by injection, for example, bolus injection or continuous infusion) and may be presented in unit dose form in ampoules, pre-filled syringes, small volume infusion containers or in multi-dose containers. As noted above, preservatives can be added to help maintain the shelve life ofthe dosage form.
  • the active peptides and other ingredients may form suspensions, solutions, or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilizing and/or dispersing agents.
  • the active peptides and other ingredients may be in powder form, obtained by aseptic isolation of sterile solid or by lyophilization from solution, for constitution with a suitable vehicle, e.g., sterile, pyrogen-free water, before use.
  • a suitable vehicle e.g., sterile, pyrogen-free water
  • These formulations can contain pharmaceutically acceptable carriers, vehicles and adjuvants that are well known in the art.
  • organic solvent(s) that is/are acceptable from the physiological standpoint, chosen, in addition to water, from solvents such as acetone, ethanol, isopropyl alcohol, glycol ethers such as the products sold under the name "Dowanol,” polyglycols and polyethylene glycols, C1-C4 alkyl esters of short-chain acids, ethyl or isopropyl lactate, fatty acid triglycerides such as the products marketed under the name "Miglyol,” isopropyl myristate, animal, mineral and vegetable oils and polysiloxanes.
  • solvents such as acetone, ethanol, isopropyl alcohol, glycol ethers such as the products sold under the name "Dowanol,” polyglycols and polyethylene glycols, C1-C4 alkyl esters of short-chain acids, ethyl or isopropyl lactate, fatty acid triglycerides such as the products marketed under the name "Mi
  • an adjuvant chosen from antioxidants, surfactants, other preservatives, film-forming, keratolytic or comedolytic agents, perfumes, flavorings and colorings.
  • Antioxidants such as t-butylhydroquinone, butylated hydroxyanisole, butylated hydroxytoluene and ⁇ -tocopherol and its derivatives can be added.
  • combination products that include one or more cyclic peptides ofthe present invention and one or more other anti-microbial agents.
  • antibiotics can be included in the pharmaceutical compositions ofthe invention, such as aminoglycosides (e.g., streptomycin, gentamicin, sisomicin, tobramycin and amicacin), ansamycins (e.g. rifamycin), antimycotics (e.g. polyenes and benzofuran derivatives), ⁇ - lactams (e.g.
  • aminoglycosides e.g., streptomycin, gentamicin, sisomicin, tobramycin and amicacin
  • ansamycins e.g. rifamycin
  • antimycotics e.g. polyenes and benzofuran derivatives
  • ⁇ - lactams e.g.
  • penicillins and cephalosporins include chloramphenical (including thiamphenol and azidamphenicol), linosamides (lincomycin, clindamycin), macrolides (erythromycin, oleandomycin, spiramycin), polymyxins, bacitracins, tyrothycin, capreomycin, vancomycin, tetracychnes (including oxytetracycline, minocycline, doxycycline), phosphomycin and fusidic acid.
  • the peptides are well suited to formulation as sustained release dosage forms and the like.
  • the formulations can be so constituted that they release the active peptide, for example, in a particular part ofthe intestinal or respiratory tract, possibly over a period of time.
  • Coatings, envelopes, and protective matrices may be made, for example, from polymeric substances, such as polylactide-glycolates, liposomes, microemulsions, microparticles, nanoparticles, or waxes. These coatings, envelopes, and protective matrices are useful to coat indwelling devices, e.g., stents, catheters, peritoneal dialysis tubing, draining devices and the like.
  • the therapeutic agents may be formulated as is known in the art for direct application to a target area.
  • Forms chiefly conditioned for topical application take the form, for example, of creams, milks, gels, dispersion or microemulsions, lotions thickened to a greater or lesser extent, impregnated pads, ointments or sticks, aerosol formulations (e.g., sprays or foams), soaps, detergents, lotions or cakes of soap.
  • Other conventional forms for this purpose include wound dressings, coated bandages or other polymer coverings, ointments, creams, lotions, pastes, jellies, sprays, and aerosols.
  • the therapeutic peptides ofthe invention can be delivered via patches or bandages for dermal administration.
  • the peptide can be formulated to be part of an adhesive polymer, such as polyacrylate or acrylate/vinyl acetate copolymer.
  • an adhesive polymer such as polyacrylate or acrylate/vinyl acetate copolymer.
  • the backing layer can be any appropriate thickness that will provide the desired protective and support functions.
  • a suitable thickness will generally be from about 10 to about 200 microns.
  • Ointments and creams may, for example, be formulated with an aqueous or oily base with the addition of suitable thickening and/or gelling agents.
  • Lotions may be formulated with an aqueous or oily base and will in general also contain one or more emulsifying agents, stabilizing agents, dispersing agents, suspending agents, thickening agents, or coloring agents.
  • the active peptides can also be delivered via iontophoresis, e.g., as disclosed in U.S. Patent Nos. 4,140,122; 4,383,529; or 4,051,842.
  • the percent by weight of a therapeutic agent ofthe invention present in a topical formulation will depend on various factors, but generally will be from 0.01% to 95% ofthe total weight ofthe formulation, and typically 0.1-85% by weight.
  • Drops such as eye drops or nose drops, may be formulated with one or more ofthe therapeutic peptides in an aqueous or non-aqueous base also comprising one or more dispersing agents, solubilizing agents or suspending agents.
  • Liquid sprays are conveniently delivered from pressurized packs. Drops can be delivered via a simple eye dropper-capped bottle, or via a plastic bottle adapted to deliver liquid contents dropwise, via a specially shaped closure.
  • the therapeutic peptide may further be formulated for topical administration in the mouth or throat.
  • the active ingredients may be formulated as a lozenge further comprising a flavored base, usually sucrose and acacia or tragacanth; pastilles comprising the composition in an inert base such as gelatin and glycerin or sucrose and acacia; and mouthwashes comprising the composition ofthe present invention in a suitable liquid carrier.
  • a flavored base usually sucrose and acacia or tragacanth
  • pastilles comprising the composition in an inert base such as gelatin and glycerin or sucrose and acacia
  • mouthwashes comprising the composition ofthe present invention in a suitable liquid carrier.
  • the pharmaceutical formulations ofthe present invention may include, as optional ingredients, pharmaceutically acceptable carriers, diluents, solubilizing or emulsifying agents, and salts ofthe type that are available in the art.
  • pharmaceutically acceptable carriers such as physiologically buffered saline solutions and water.
  • diluents such as phosphate buffered saline solutions pH 7.0-8.0.
  • the peptides ofthe invention can also be administered to the respiratory tract.
  • the present invention also provides aerosol pharmaceutical formulations and dosage forms for use in the methods ofthe invention.
  • dosage forms comprise an amount of at least one ofthe agents of the invention effective to treat or prevent the clinical symptoms of a specific infection, indication or disease. Any statistically significant attenuation of one or more symptoms of an infection, indication or disease that has been treated pursuant to the method ofthe present invention is considered to be a treatment of such infection, indication or disease within the scope ofthe invention.
  • the composition may take the form of a dry powder, for example, a powder mix of the therapeutic agent and a suitable powder base such as lactose or starch.
  • the powder composition may be presented in unit dosage form in, for example, capsules or cartridges, or, e.g., gelatin or blister packs from which the powder may be administered with the aid of an inhalator, insufflator, or a metered-dose inhaler (see, for example, the pressurized metered dose inhaler (MDI) and the dry powder inhaler disclosed in Newman, S . P. in Aerosols and the Lung,
  • MDI pressurized metered dose inhaler
  • the dry powder inhaler disclosed in Newman, S . P. in Aerosols and the Lung
  • Therapeutic peptides ofthe present invention can also be administered in an aqueous solution when administered in an aerosol or inhaled form.
  • other aerosol pharmaceutical formulations may comprise, for example, a physiologically acceptable buffered saline solution containing between about 0.1 mg/ml and about 100 mg/ml of one or more ofthe peptides ofthe present invention specific for the indication or disease to be treated.
  • Dry aerosol in the form of finely divided solid peptide or nucleic acid particles that are not dissolved or suspended in a liquid are also useful in the practice ofthe present invention.
  • Peptides ofthe present invention may be formulated as dusting powders and comprise finely divided particles having an average particle size of between about 1 and 5 ⁇ m, alternatively between 2 and 3 ⁇ m.
  • Finely divided particles may be prepared by pulverization and screen filtration using techniques well known in the art.
  • the particles may be administered by inhaling a predetermined quantity ofthe finely divided material, which can be in the form of a powder.
  • the unit content of active ingredient or ingredients contained in an individual aerosol dose of each dosage form need not in itself constitute an effective amount for treating the particular infection, indication or disease since the necessary effective amount can be reached by administration of a plurality of dosage units.
  • the effective amount may be achieved using less than the dose in the dosage form, either individually, or in a series of administrations.
  • the therapeutic peptides ofthe invention are conveniently delivered from a nebulizer or a pressurized pack or other convenient means of delivering an aerosol spray.
  • Pressurized packs may comprise a suitable propellant such as dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
  • the dosage unit may be determined by providing a valve to deliver a metered amount.
  • Nebulizers include, but are not limited to, those described in U.S. Patent Nos.
  • Aerosol delivery systems ofthe type disclosed herein are available from numerous commercial sources including Fisons Corporation (Bedford, Mass.), Schering Corp. (Kenilworth, NJ) and American Pharmoseal Co., (Valencia, CA).
  • the therapeutic agent may also be administered via nose drops, a liquid spray, such as via a plastic bottle atomizer or metered-dose inhaler.
  • Typical of atomizers are the Mistometer (Wintrop) and the Medihaler (Riker).
  • the active ingredients may also be used in combination with other therapeutic agents, for example, pain relievers, anti-inflammatory agents, antihistamines, bronchodilators and the like, whether for the conditions described or some other condition.
  • other therapeutic agents for example, pain relievers, anti-inflammatory agents, antihistamines, bronchodilators and the like, whether for the conditions described or some other condition.
  • the present invention further pertains to a packaged pharmaceutical composition for controlling microbial infections such as a kit or other container.
  • a packaged pharmaceutical composition for controlling microbial infections such as a kit or other container.
  • the kit or container holds a therapeutically effective amount of a pharmaceutical composition for controlling microbial infections and instructions for using the pharmaceutical composition for control ofthe microbial infection.
  • the pharmaceutical composition includes at least one cyclic peptide ofthe present invention, in a therapeutically effective amount such that microbial infection is controlled.
  • Solvents and reagents Acetonitrile (ACN, optima grade), dichloromethane (DCM, ACS grade), N,N-dimethylformamide (DMF, sequencing grade), diethyl ether (Et O, ACS grade), N,N-diisopropylethylamine (DIEA, peptide synthesis grade) were purchased from Fisher and used without further purification.
  • ACN Acetonitrile
  • DCM dichloromethane
  • DMF N,N-dimethylformamide
  • Et O diethyl ether
  • DIEA N,N-diisopropylethylamine
  • Trifluoroacetic acid (TFA, New Jersey Halocarbon), 2-(lH- benzotriazol-l-yl)-l,l,3,3-tetramethyluronium hexafluorophosphate (HBTU, Richelieu Biotechnologies), benzotriazole-1-yl-oxy-tris-pyrrolidino- phosphonium hexafluorophosphate (PyBOP, Novabiochem) were used as obtained.
  • Commercially available amino acids and resins were used as obtained from Bachem, Novabiochem or Advanced Chemtech.
  • the side-chain protections were as follows.
  • N-terminal Fmoc group was removed by treatment with 20%) Piperidine/DMF.
  • the peptide containing resin was washed with DMF (3x20 mL), then with DCM (3x20 mL).
  • the side chain protected linear peptide was cleaved from the resin by sequential shaking with several portions (10-20) of TFA DCM mixture (1/99) collecting the solution into a flask, containing pyridine (2 mL) and MeOH (5 mL). The completion ofthe cleavage is achieved when the resin changed its color to dark red. Then the resin was washed with DCM (2x 10 mL) and MeOH (2x 10 mL) . These washings were combined with collected TFA cleavage solutions.
  • Cyclization was performed in DMF at a peptide concentration of 1-5 mM using a mixture of PyBOP (5 eq. with respect to crude peptide) and DIEA (40 eq.). The amount of DIEA was adjusted to achieve an apparent pH 9-10, which was assessed by applying a drop of reaction mixture to a wet pH paper.
  • the TFA solution was concentrated by 5 times by evaporation under vacuum (1 mm Hg), from which the peptide was precipitated by adding it to an ice-cold Et 2 O.
  • the purity of dried crude peptides was assessed by HPLC and MALDI-MS.
  • the crude peptides can be partially purified by dissolving in boiling ACN/water/HCl mixture (30/70/0.1) and cooling the turbid solution in a refrigerator. Hi case of peptide high solubility in this mixture, the precipitate can be obtained by adding acetone (3 vol. eq.) to the above solution.
  • N-Boc- ⁇ -Fmoc-glutamic acid was loaded onto methyl- benzhydrylamine (MBHA) resin through its side chain carboxylate, then the resin was split into four equimolar fractions of 0.25 mmol each for the rest ofthe synthesis.
  • MBHA methyl- benzhydrylamine
  • the specified amino acids ofthe peptide library sequences showing the greatest biological activity (lowest MIC value) were retained for the generation ofthe next set of libraries.
  • Subsequent generations of peptide libraries were synthesized in a similar fashion, with the splitting ofthe resin after the coupling ofthe specified amino acids determined from the previous generation.
  • the peptides ofthe combinatorial libraries were identified by electrospray-mass spectrometry ( ⁇ S-MS) or MALDI-TOF mass spectrometry.
  • Cyclic D, E- ⁇ -peptide combinatorial libraries were prepared using a one- bead-one-compound strategy on macrobeads by a split and pool method. See, K.S. Lam, M. Lebl, V. Krchnak, "The One-bead-one-compound' combinatorial library method," Chem. Rev. 1997, 97, 411-448. Each bead contained a single sequence and was dispersed into microtiter plates using a density of one bead per well. Cleavage ofthe peptide from a single bead provided about 70-80 ⁇ g of peptide per well. This amount of peptide could be used for approximately 100 in vitro anti-microbial assays. Mass spectrometric peptide sequencing strategies were used for rapid identification of selected peptide species within a given library.
  • Solid-phase peptide synthesis was performed on polystyrene macrobeads functionalized with a TFA-labile trityl linker, which considerably facilitated the synthesis, handling, solid-phase cyclization, and final side chain deprotection and peptide isolation.
  • the growing peptide chain was linked through the first amino acid side chain (for example lysine or histidine) to the trityl moiety allowing for selective "head-to-tail" cyclization ofthe completed peptide sequence on solid support.
  • the ⁇ -carboxyl group ofthe first N- ⁇ -Fmoc amino acid was protected as an allyl ester.
  • Resin loading and peptide chain elongation was performed under standard Fmoc solid phase peptide synthesis conditions using chlorotrityl polystyrene macrobead resin (500-560 um, Peptides International) as the solid support, with HBTU as a coupling reagent and 20% > piperidine in DMF for Fmoc deprotection. After completion ofthe final amino acid coupling, the resin was exposed to palladium tetrakis(triphenylphosphine) and N-methyl morpholine to remove the C-terminal allyl protecting group.
  • Peptide libraries obtained by the above procedure were sufficiently pure for use in anti-microbial selection assays.
  • Materials: Acetonitrile (HPLC grade), dichloromethane (optima grade), dicyclohexylamine (DCHA), diethyl ether (anhydrous), dimethylformamide (sequencing grade), diisopropylethylamine (DIPEA, peptide synthesis grade), and piperidine (anhydrous) were purchased from Fisher and used without further purification.
  • Trifluoroacetic acid (TFA, New Jersey Halocarbon), and 2-(l-H- benzotriazol-l-yl)-l,l,3,3-tetramethyluronium hexafluorophosphate ( ⁇ BTU, Novabiochem), benzotriazole 1-yl-oxy-tris-pyrrolidino-phosphonium hexafluorophosphate (PyBOP, Novabiochem) were used without further purification. Tetrakistriphenylphosphine palladium(O) was purchased from Strem Chemicals.
  • N-Fmoc amino acids for solid-phase peptide synthesis and trityl chloride PS 1%> DNB, substitution 0.5 - 1.05 mmol g "1 ) resin were used as obtained from Novabiochem or Bachem.
  • Trityl chloride macrobead resin was obtained from Peptides International.
  • Fmoc-Lysine(Boc)-0 allyl Preparation of Fmoc-Lysine(Boc)-0 allyl.
  • Fmoc-Lysine(Boc)-O Allyl was made according to the protocol of Kates, S. A.; Sole, N. A.; Johnson, C. R.; Hudson, D.; Barany, G.; Albericio, F. Tetrahedron Lett. 1993, 34, 1549-1552. r-
  • Fmoc-Lys-(Boc)-OH (5 g, 10.6 mmol) was added to allyl bromide (25 mL, 0.29 mol), followed by DIPEA (3.73 mL). This mixture was heated at 90 °C for 1 h. The reaction was allowed to cool, concentrated by rotary evaporation, and after dilution with ethyl acetate was washed with 2 x 0.1 N HCI, 2 x saturated sodium bicarbonate at pH ⁇ 9.5, followed by brine. The organic layer was filtered through a pad of silica gel and concentrated to afford a solid. This solid was washed with ether to provide a white powder that was used directly in the next step.
  • Trityl chloride resin was swollen in dry deacidified (Na 2 CO 3 ) dichloromethane for 20 min. A solution of Fmoc-Lys-OAllyl in dichloromethane was added to the resin, immediately followed by 4 eq. of DIPEA. After shaking for 2 hours the resin was washed resin with dichloromethane, then shaken with 10% MeOH: 10% DIPEA: 80% dichloromethane for 10 min. After washing with dichloromethane and drying in vacuo the resin loading was evaluated based on Fmoc released monitored by UN absorption at 290 nm.
  • Peptide Synthesis Peptides were synthesized using standard solid-phase Fmoc protocols (see Wellings, D. A.; Atherton, E. Methods Enzymol. 1997, 289, 44-67) on the Fmoc-Lys-OAllyl loaded trityl resin. Following synthesis ofthe linear peptide the resin was swollen in dry dichloromethane for 20 min. To the resin was added a degassed solution of 0.5 eq. Pd(PPh 3 ) 4 in 90%> CHC1 : 10%> 4- methylmorpholine.
  • the antimicrobial activity ofthe peptides was determined using a broth dilution assay essentially as descried in the guidelines ofthe National Committee for Clinical Laboratory Standards (NCCLS) [National Committee for Clinical Laboratory Standards. Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically. Fourth edition. Approved Standard (1997). Document M7-A4. (NCCLS, Villanova, Pennsylvania, 1997].
  • Test tubes macrodilution method
  • microtiter plates microdilution method containing two-fold serial dilution of peptides were inoculated with various bacterial cultures. Controls included non-inoculated medium (sterility), vehicle control, and various commercially available antibiotics for which minimal inhibitory concentrations against tested organisms were known.
  • VanB Gram Vancomycin resistant Enterococcus ATCC 51299 Gram Vancomycin resistant (vanB); faecalis positive resistant to vancomycin, gentamicin and streptomycin.
  • VanA Gram Vancomycin resistant
  • peptide solutions Preparation of peptide solutions.
  • Serial 2-fold dilutions were made in the above DMSO/aq. sucrose (9%) mixture with concentrations ranging approximately 400-2 ⁇ g/ml and aliquots were dispensed in test tubes (100 ⁇ l) for the macrodilution test or in microtiter plates (20 ⁇ l) for the microdilution assays.
  • Inoculum preparation Overnight cultures of different microorganisms grown in suitable media were diluted 4000 times to an approximate inoculum size of 2.5 x 10 5 cfu ml.
  • Macrodilution method Macrodilution methods were performed using procedures similar to those described in the National Committee for Clinical Laboratory Standards. Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically. Fourth edition. Approved Standard (1997).
  • Microdilution method Microdilution methods were performed using procedures similar to those described in the National Committee for Clinical Laboratory Standards. Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically. Fourth edition. Approved Standard (1997). Document M7-A4. (NCCLS, Villanova, Pennsylvania, 1997. Eighty ⁇ l aliquots ofthe above inoculum were dispensed into 96-well microtiter plates containing different peptide solutions and incubated for 18 h at 37 "C with shaking (plates were sealed with parafilm to avoid excessive evaporation of culture medium) and MIC's were recorded. Each assay was performed at least twice and errors were typically + one dilution. MBC Determination
  • MBC Minimum bactericidal concentrations
  • Red blood cells were then treated with serial dilutions of test peptides in a 96 well plate at 37 °C for 30 minutes.
  • Control samples included a saline solution and 1 % Triton X-100 as 0 and 100 % hemolysis, respectively. In some cases, mellitin was used as a further control.
  • Mellitin is a linear peptide that is hemolytic against mammalian red blood cells in vitro at a concentration of about 10 ⁇ g/ml. Plates were centrifuged at 1000 g for 10 minutes. Aliquots of the supernatant were diluted 2 times with saline solution and the absorbance was measured at 560 nm. Cytotoxicity assay
  • Toxicity of cyclic peptides to mammalian cell cultures was determined by a modified method based on procedures described in Promega Technical Bulletin No. 169 "CellTiter 96 Aqueous Non-Radioactive Cell Proliferation Assay” and in Chapter 16 "MTT Assays” from Methods in Molecular Biology, Vol 43: in vitro toxicity testing protocols.
  • Cells were seeded at appropriate density (5x10 4 cell per ml for rat hepatocyte cell line H4IIE) in a growth medium in a 96-well microtiter plate (90 ⁇ l/well) and allowed to attach and grow for 24 hours at 37°C in presence of 5% CO 2 in a humidified incubator.
  • Cyclic peptide solutions (including serially diluted solutions) and control compound solutions in 5% DMSO were added into wells containing growing cells (10 ⁇ l per well). Triplicate wells per dilution of each peptide were prepared. Cells were exposed to compounds for 24 hours at 37°C in presence of 5% CO in a humidified incubator. MTS (Promega) and PMS (Sigma) reagents were added to the wells to final concentrations of 333 ⁇ g/ml and 25 ⁇ M, respectively, after 24 hour incubation. Pre-read plates at 490 nm in a reader to obtain background ODs for each well. Plates were read again after 3 hours of incubation at 37°C in presence of 5% CO 2 . Net changes in OD 49 o for each well ofthe plates were used to calculate % inhibition of cell growth by a compound at a given concentration (as compared to a growth control using just solvent).
  • Bacteria Preparation for In Vivo Protection Testing Bacteria were prepared for in vivo using procedures similar to those as previously described. See V. Lorian, Antibiotics in Laboratory Medicine, Williams and Wilkins, Baltimore 1991. S. aureus MRS A bacteria (ATCC 33591) were grown at 37 °C in 5 mL of Antibiotic Medium-3 (AM-3, Difco Laboratories) with agitation for 12 hours to a stationary phase. Cells were collected by centrifugation, washed twice with saline solution and resuspended in about 10 mL of saline to an O.D. 65 o of 1.2.
  • mice Male Balb-C in groups of 4-8 were given via IN, IP or SQ single bolus doses of peptides and monitored for 14 days. Toxicity of sub-lethal doses was assessed based on the behavior and appearance ofthe mice after peptide administration compared to control mice receiving only vehicle. Signs of acute toxicity included lack of activity, red feet and tail, faster breathing. Death was defined as the end point for lethal doses of peptides. Pathology Studies
  • Pathology effects of peptides cyclo[RRKWLWLW]-HCl and cyclo- [KQRWLWLW]-HC1 were accessed with Balb-C (male 20-25 g). Peptides were administered IP at a lethal dose of 75 mg/kg in 9% sucrose, along with control mice that received vehicle alone. After 50-60 min (in case of cyclo[KQRWLWLW]-HCl), and on the next day (in case of cyclo[RRKWLWLW]-HCl) mice were sacrificed and analyzed (Dr. Osborn, Net. Pathologist, Department of Animal Resources, TSRI). Pathology studies included blood cell count, and histology examination of different tissues and organs.
  • mice Male CD-I, Charles River labs, 20-25 g were used for this study.
  • mice On day eleven mice were sacrificed and analyzed (Dr. Osborn, Net. Pathologist, Department of Animal Resources, TSRI). Pathology studies included blood cell count, and histology examination of different tissues and organs.
  • mice IN into the tail vein of Balb/C mice at a dose of 3.6 mg/kg. Then the blood was collected immediately from one group of mice (3 mice per group) by bleeding the tail, separately from each mouse (50-100 ⁇ L per mouse). Further collections of blood were done from other groups of mice at times 20, 40, 70, 90, 120, 180, and 260 min after injection. Plasma from each blood sample was separated immediately after collection by spinning down red blood cells over a period of 5 min at 4000 rev./min. The plasma was then diluted with an equal volume of saline and refrigerated until analysis. Storage of samples under these conditions over a period of 1 month did not change the concenfration of peptide.
  • IP injection Solutions of peptide in 9% sucrose (8.1 mg/mL) were injected IP into Balb/C mice at a dose of 100 mg/kg. Blood was collected immediately from one group of mice (3 mice per group) by bleeding the tail, separately from each mouse (50-100 ⁇ L per mouse). Further collections of blood were done from other groups of mice at times 0.5, 1, 2, 4, 6, 10, 15 h after , injection. Plasma from each blood sample was separated immediately after collection by spinning down red blood cells over a period of 5 min at 4000 rev./min. Plasma was then diluted with equal volume of saline and refrigerated until analysis. Storage of samples under these conditions over a period of 1 month did not change the concentration of peptide.
  • Detection /cyclo[RRKWLWLW]-HCl in plasma by HPLC Diluted with saline plasma (50-100 ⁇ L) was added to an eluent A (0.1 %> HCI in 99% H 2 O/l% AC ⁇ (v/v)) (150-300 ⁇ L), vortexed, and partial precipitation was removed by centrifugation.
  • the clear solution was injected into an HPLC and the peptide was detected at 280 nm, in the 8-10 min interval, using a gradient of eluent A (0.1 % HCI in 99% H 2 O/l% ACN (v/v)) and eluent B (0.07 % HCI in 10% H 2 O/90% ACN (v/v)) using a flow rate of 1.5 l/min.
  • the following gradient was used: 30 to 30 % B (5 min), followed by 30 to 37% B (5 min), followed by 37 to 40% B (12.5 min).
  • IV injection Solution of peptide in 9% sucrose (2 mg/mL) was injected IV into the tail vein of Balb/C mice at a dose of 5 mg/kg. Blood was then collected immediately from one group of mice (3 mice per group) by bleeding the tail, separately from each mouse (50-100 ⁇ L per mouse). Further collections of blood were done from other groups of mice at times 30, 60, 120, 230, and 300 min after injection. Plasma from each blood sample was separated immediately after collection by spinning down red blood cells over a period of 5 min at 4000 rev./min. Plasma was then diluted with an equal volume of saline and refrigerated until analysis. Storage of samples under these conditions over a period of 1 month did not change the concentration of peptide.
  • IP injection Solution of peptide in 9% sucrose (9.8 mg/mL) was injected IP into Balb/C mice at a dose of 100 mg/kg. Blood was then collected immediately from one group of mice (3 mice per group) by bleeding the tail, separately from each mouse (50-100 ⁇ L per mouse). Further collections of blood were done from other groups of mice at times 0.5, 1, 2, 4, 6, 10 h after injection. Plasma from each blood sample was separated immediately after collection by spinning down red blood cells over a period of 5 min at 4000 rev./min. Plasma was then diluted with an equal volume of saline and refrigerated until analysis. Storage at these conditions over a period of 1 month did not change the concentration of peptide.
  • Detection o/c(KSKWLWLW) HCI in plasma by HPLC Samples were diluted with saline plasma (50-100 ⁇ L), added to an equal volume of eluent A (0.1 % TFA in 96.5% H 2 O/0.9% ACN/2.4% MeOH (v/v)), vortexed, and partial precipitation was removed by centrifugation.
  • the clear solution was injected into HPLC and the peptide was detected at 280 nm, in the 18-20 min interval, using a gradient of eluent A (0.1 % TFA in 96.5% H 2 O/0.9% ACN/2.4% MeOH (v/v)) and eluent B (0.05 % TFA in 8% H 2 O/72% ACN/20% MeOH (v/v)) using a flow rate of 1.5 ml/min. The following gradient was used: 0 to 0 % B (5 min), followed by 0 to 100% B (25 min).
  • Exemplary detection method of cyclic peptides in serum e.g., cfRRKWLWLWJ: Serum sample extraction was accomplished as follows.
  • Blank serum was spiked with c[RRKWLWLW] to construct standard curve for quantitative purpose.
  • Serial dilutions were used to prepare the serum standards of 10, 5, 2, 1, 0.5, 0.25, and 0. lug/ml.
  • 50ul of each serum standard and any unknown sample was extracted by lOOul ice-cold Acetonitrile.
  • the supernatant was transferred to HPLC vial inserts and 60ul injected onto HPLC column.
  • Samples were analyzed by Sciex API2000 triple-quad LCMS system. MS was pre-tuned for voltages and flow parameters to assure optimum sensitivity for the compound.
  • the HPLC system consists of an Agilent 1100 series controller, binary pump, autosampler and an UV detector.
  • the column was a Waters Atlantics C18 (2.1x150mm) maintained at room temperature.
  • Mobile phase consisted of 60% A (nano-H2O with 0.1 % Formic Acid) and 40% B (Acetonitrile) using isocratic method.
  • the flow rate was 250 ⁇ L/min.
  • c[RRKWLWLW] peak eluted at 2.17 minute.
  • Equation (2) was used to determine bioavailabihty (F) of peptide injected via IP route
  • Dr and D ⁇ > are doses of peptide administered via IV and IP routes respectively, expressed in mg kg.
  • the eight-residue cyclic peptides used in the first experiments of this example had three consecutive polar residues and E-tryptophan and D-leucine repeats that form a hydrophobic surface to promote effective partitioning onto cell membranes. H addition, peptides were most often designed to include at least one basic amino acid residue in order to enhance specificity toward bacterial membranes. The utility of these design features was demonstrated by in vitro antibacterial assays employing a representative cyclic peptide with sequence Lys-D-Gln-Arg-D-Trp-Leu-D-Trp-Leu-D-Trp (SEQ ID NO:9).
  • Cyclic peptide SEQ ID NO:9 displayed potent activity against gram positive Bacillus subtilis and Staphylococcus aureus and against gram negative Streptococcus pneumonieae and vancomycin-resistant Enterococcus faecalis (Table 4).
  • a series of six- and eight-residue amphiphilic cyclic peptides were made to further probe the antibacterial activity of these peptides as antibacterial agents and to examine the relationship between surface properties, antibacterial activities, and membrane selectivity.
  • Peptides were synthesized by standard solid-phase BOC or FMOC synthetic protocols, cyclized in solution or on solid support, purified by RP-HPLC, and characterized by MALDI-TOF or ESI-mass spectrometry. The sequences of these peptides are provided in Table 5. Shorthand representation of cyclic peptide sequences using single letter codes was used to allow facile sequence comparisons. Underlining indicates that amino acid is a D-amino acid residue.
  • Cyclic peptides with SEQ ID NO:5 and 6 each bear one basic residue between two serine residues, or between a serine and a threonine residue, respectively. While peptide SEQ ID NO:5 [cyclo-(D-Ser-Lys-D-Ser-T ⁇ -D-Leu- T ⁇ -D-Leu-T ⁇ )] displays good activity against S.
  • SEQ ID NOs: 17-22 provided high activities against S. aureus MRS A.
  • Peptides with SEQ ID NO: 18 [cyclo-(D-Arg-Arg-D-Lys-T ⁇ -D-Leu-T ⁇ -D-Leu-T ⁇ )] and SEQ ID NO:21 [cyclo-(D-His-Lys-D-His-T ⁇ -D-Leu-T ⁇ -D-Leu-T ⁇ )] also exhibited moderate activities against E. coli.
  • the in vitro antibacterial activities of hexameric peptides with SEQ ID NOs:26-29 also indicate that use of basic amino acids in the cyclic peptides may increase antibacterial activity and improve selectivity for bacterial membranes.
  • Peptide SEQ HD NO:26 [cyclo-(D- Lys-Lys-D-Leu-T ⁇ -D-Leu-T ⁇ )], with two consecutive lysine residues, exhibits broad-spectrum activity and has low hemolytic properties.
  • peptide SEQ ID NO:27 [cyclo-(D-Lys-His-D-Leu-T ⁇ -D-Leu-T ⁇ )], which has a histidine instead ofthe lysine in peptide SEQ ID NO:26, retains high activity against S. aureus MRSA but is inactive against E. coli.
  • Cyclic peptides having SEQ ID NO:13, 18, 26, and 29 were assayed for proteolytic susceptibility.
  • the peptides show abiotic structure and conformational preferences, and were stable in the presence of trypsin, - cliymotrypsin, subtilisin, and blood plasma. No significant peptide degradation was observed in chromatograms obtained from RP-HPLC over a 24 h time period, whereas control linear L- ⁇ -amino acid peptides were degraded in less than 10 min under similar reaction conditions and within four hours when placed in murine blood plasma.
  • Results for further testing of gram-negative and gram-positive bacteria are shown in Tables 7 and 8 respectively, along with control assays using FDA approved antibiotics.
  • the shorthand representation of cyclic peptide sequences was utilized where single amino acid letter codes are employed to facilitate sequence comparisons. Underlining indicates that amino acid is a D-amino acid residue and brackets indicate that the peptides are circular.
  • cyclic peptides ofthe invention are further illustrated in Table 9.
  • Each cyclic peptide is described in shorthand using underlining to indicate which amino acids have D-chirality, brackets to identify cyclic peptides and a number in parentheses to indicate the SEQ ID NO: (i.e., NO:). These peptides were tested against methicillin-resistant
  • MRSA Staphylococcus aureus
  • VRE Enterococcus faecalis
  • VRE Enterococcus faecalis
  • cyclic peptides ofthe invention was tested against a larger variety of bacterial species.
  • the bacterial species tested were as follows: Vancomycin resistant Enterococcus faecalis (VRE, ATCC 51575); methicillin resistant Staphylococcus aureus (ATCC 33591, MRSA); E. coli: JM109 (DE3) Bacillus cereus (ATCC11778); and Streptococcus pneumoniae (ATCC 6301).
  • Murine red blood cells were used for the hemolysis assays as described in Example 1.
  • D-Lys-His- D-Leu-T ⁇ - D-Leu-T ⁇ (SEQ ID NO:27); D-Lys-Arg- D-Lys-T ⁇ - D-Leu-T ⁇ - D-Leu-T ⁇ (SEQ HD NO:19); D-Lys-Gln- D-Arg-T ⁇ - D-Leu-T ⁇ - D-Leu-T ⁇ (SEQ HD NO:8); D-Lys-Lys- D-Leu-T ⁇ - D-Leu-T ⁇ (SEQ ID NO:26);
  • the log ofthe number of colony forming units (cfu) per ml of culture was determined as a function of time after treatment of S. aureus (MRSA) (ATCC No. 33591) with cyclo[KHLWLW] (closed circles), cyclo [KRKWLWLW] (closed triangles), and cyclo [KQRWLWLW] (open squares) at MIC concentrations.
  • MRSA S. aureus
  • MRSA S. aureus
  • H Figure 8b the log ofthe number of E. coli colony forming units (cfu) per ml of culture is plotted versus time treated with cyclo [KRKWLWLW] (closed triangles), cyclo [KQJRWLWLW] (closed circles), cyclo[KHLWLW] (closed squares), and cyclo[KKLWLW] (open squares) at MIC concentrations.
  • cyclo [KQRWLWLW] kills effectively all the E. coli within about thirty minutes.
  • Cyclic peptide cyclo [KHLWLW] kills effectively all E. coli within about 90 minutes.
  • Figures 9 and 10 illustrate the time course for killing S. aureus (MRS A) (ATCC No. 33592) with varying concentrations of cyclo [KSKWLWLW] cyclic peptide (SEQ ID NO: 12) at room temperature and at 37° C.
  • the KSKWLWLW cyclic peptide appears to kill effectively all bacteria within about one hour. However, the bacterial population rebounds by about six hours. This may be due to growth of a few survivors after the residual cyclic peptide within the culture has been exhausted because the amount of peptide employed in that assay was below the MIC value.
  • MRSA S. aureus
  • FIGS 11 and 12 illustrate the time course for killing E. faecium SP180 with varying concentrations of KSKWLWLW (SEQ ID NO: 12), at room temperature and at 37° C. Assays were performed in Brain Heart Infusion broth. As illustrated, somewhat shorter times and/or somewhat lower concentrations of this cyclic peptide are required to kill E. faecium SP180 at 37° C than at room temperature.
  • E. faecium SP180 is vancomycin resistant (vanA) and multiply resistant to several FDA approved antibiotics. For example, at 37° C, about 2 ⁇ g/ml of KSKWLWLW can kill effectively all bacteria faster than an aliquot can be removed from the test culture for assessing the number of surviving cfu.
  • vanA vancomycin resistant
  • FIGS 13 and 14 illustrate the time course for killing S. aureus (MRS A) (ATCC No. 33592) with varying concentrations of RRKWLWLW (SEQ ID NO: 18), at room temperature and at 37° C.
  • MRSA S. aureus
  • FIGS 15 and 16 illustrate the time course for killing E. faecium SP180 with varying concentrations of RRKWLWLW (SEQ ID NO: 18) at room temperature and at 37° C.
  • E. faecium SP180 is vancomycin resistant (vanA) and multiply resistant to several FDA approved antibiotics. Assays were performed in Brain Heart Infusion broth. As illustrated, somewhat shorter times and/or somewhat lower concentrations of this cyclic peptide are required to kill E. faecium SP180 at 37° C than at room temperature. For example, at both room temperature and at 37° C, about 2 ⁇ g/ml of RRKWLWLW (SEQ ID NO: 18) can kill effectively all bacteria within one hour. Hence, the RRKWLWLW (SEQ ID NO : 18) cyclic peptide is highly effective against E. faecium SP 180 bacteria at both room temperature and at 37°C.
  • cyclic peptides may operate to kill microbes.
  • Another mechanism by which the cyclic peptides may kill microbes is through a receptor that recognizes the cyclic peptides as ligands. See Friederich et al., Antimicrob. Agents Chemother. 44, 2086-2092(2000); Amsterdam, D. in Antibiotics in Laboratory Medicine, 3rd ed. (ed. Lorian, N.) 53-105 (Baltimore, Maryland, USA, 1991).
  • a receptor/ligand-mediated mode of action for the cyclic peptides in bacterial membranes is unlikely for several reasons.
  • cyclic peptides with diverse structures are active against microbes, but most receptors discriminate between potential ligands on the basis of structure, and will only recognize ligands having defined structural features.
  • the peptides ofthe invention kill bacteria very quickly whereas a receptor/ligand-mediated binding/inhibition mechanism would typically be expected to take several hours to achieve complete bactericidal or bacteriostatic activity. This example provides biophysical data that supports a membrane depolarization mechanism of action.
  • cyclic peptides with activity is illustrated by enantiomeric peptides having SEQ ID NO: 8 (cyclo-[D-Lys-Gln-D-Arg-T ⁇ -D- Leu-T ⁇ -D-Leu-T ⁇ ]) and SEQ HD NO:9 (cyclo-[Lys-D-Gln-Arg-D-T ⁇ -Leu-D- T ⁇ -Leu-D-T ⁇ ]).
  • SEQ ID NO: 8 cyclo-[D-Lys-Gln-Arg-D-T ⁇ -Leu-D- T ⁇ -Leu-D-T ⁇ ]
  • SEQ HD NO:9 cyclo-[Lys-D-Gln-Arg-D-T ⁇ -Leu-D- T ⁇ -Leu-D-T ⁇ ]
  • Such a receptor-ligand mechanism would likely require more time to kill bacteria than the short time periods shown in Figures 8-16.
  • octameric peptides having SEQ ID NO:8 and SEQ HD NO:19, and hexameric peptides having SEQ ID NO:26 and SEQ ID NO:27 at concentrations equal to or above the MIC have complete bactericidal activity against S. aureus MRS A within 5 and 60 minutes, respectively.
  • time-killing studies are provided in the previous Example. hi this Example, cyclic peptides were tested to determine whether they would exhibit cellular depolarization activity.
  • the fluorescence ofthe cyanine membrane dye 3,3'-dipropylthiadicarbocyanide is sensitive to changes in bacterial membrane potential, and was employed in this Example to follow the effects of peptide SEQ ID NO:8, 18 and 26 on membrane depolarization of live S. aureus (ATCC 25923). See, Sims et al., Biochemistry 13, 3315-3330 (1974); Waggoner, Annu. Rev. Biophys. Bioeng. 8, 847-868 (1979); Loew, Adv. Chem. Ser. 235 (Biomembrane Electrochemistry), 151-173 (1994).
  • the biophysical analyses performed in synthetic lipid membranes also support a membrane permeation mode of action.
  • the peptide SEQ HD NO:2 (cyclof- Gln-D-Leu-(T ⁇ -D-Leu) 3 ]) facilitates only the transport of analytes that are smaller than its internal diameter across liposome membranes and according to ATR-FTIR analysis in DMPC multibilayes, assembles into a tube-like structure that is oriented pe ⁇ endicular to the membrane plane. Therefore, the single nanotube through-pore mechanism it is a likely mode of function for this peptide (see Figure 2a).
  • the homologous peptide SEQ ID NO:3 (cyclo[-Lys- D-Leu-(T ⁇ -D-Leu) 3 ]), having a polar charged side chain likely forms a different supramolecular structure with an opening that is larger than the internal tube diameter because it facilitates transport of larger molecules of up to approximately 10,000 MW across membranes.
  • the supramolecular structure formed from peptides having SEQ HD NO:3 (cyclo[-Lys-D-Leu-(T ⁇ - D-Leu) 3 ]) maintains an orientation in synthetic membranes that is pe ⁇ endicular to the membrane plane according to ATR-FTIR analysis.
  • Table 11 ATR-FTIR data and orientation of antibacterial cyclic peptide nanotubes in oriented DMPC lipid multibilayers.
  • Tilts refer to the angle ofthe molecular axis with respect to the surface normal.
  • DMPC dimyristoyl phosphatidylcholine. Data are average of two samples with errors ⁇ 2°.
  • Bacteria S. aureus, ATCC 25923 were treated with cyclic peptide cyclo[KSKWLWLW] for 120 minutes at room temperature and then prepared for thin section electron microscopy by standard procedures.
  • Figures 21-23 illustrate the membrane effects caused by cyclic peptides ofthe invention as observed using the electron microscope.
  • Figure 21 provides a thin section electron microscopy image of untreated S. aureus (ATCC 25923) displaying a normal intact membrane.
  • Figures 22 and 23 provide thin section electron microscopy images of S. aureus (ATCC 25923) after exposure to
  • Evidence thus indicates an anti-microbial activity based at least in part on membrane permeation, depolarization, and/or lysis.
  • Such evidence includes that the cyclic peptides act very quickly to kill microbes, that diverse cyclic peptide structures described here show anti-microbial activity, that the cyclic peptides can depolarize microbial membranes, that attenuated total reflectance (ATR) FT- IR spectroscopy studies are consistent with a membrane permeation mechanism of action rather than a receptor/ligand-mediated binding/inhibition mechanism, and that electron microscopy reveals an effect ofthe cyclic peptides ofthe invention on membrane structure.
  • ATR attenuated total reflectance
  • EXAMPLE 4 Anti-microbial Activity In Vivo Toxicology Studies Initial toxicology studies in mice were conducted to evaluate various routes of drug administration, maximum tolerable dose, and blood and tissue toxicity. Two mice in each dose study were injected with a bolus intravenous (TV), intraperitoneal (IP), or subcutaneous (SQ) doses of peptide SEQ ID NO:8, 18, and 26. For each study, two control animals received vehicle only and no peptide. Studies with peptide SEQ HD NO: 8 indicate that bolus IN injections of 12 mg/kg cause signs of temporary ( ⁇ 10 min in duration) discomfort. In contrast, no signs of toxicity were observed at the maximum tested dose (12 mg/kg) with the IP route of administration.
  • TV bolus intravenous
  • IP intraperitoneal
  • SQL subcutaneous
  • Peptide SEQ HD ⁇ O:26 was tolerated up to the maximum tested H? dose (50 mg/kg), with the highest dose causing signs of acute toxicity that were not observable after one hour. Signs of acute toxicity included any one ofthe following: lack of activity, red feet and tail, or faster breathing. Peptide SEQ ID NO: 18 was tested up to 17.5 mg/kg IP and SQ doses without any apparent signs of toxicity. A regimen of 17.5 mg per day of peptide SEQ HD NO: 18 for three consecutive days was administered to two mice IP and two mice SQ. Over four days, no apparent changes in the physical, social, and feeding activities were observed in these mice relative to control mice injected with vehicle without peptide.
  • mice (2-5x10? cfu/mouse).
  • peptide bolus doses of 0 (vehicle only), 10, 20, and 40 mg/kg were administered subcutaneously (SQ) in the upper neck compartment soon after MRSA injection.
  • SQ subcutaneously
  • mice 5 bolus peptide doses each 0 (vehicle only), 2.5, and 5 mg/kg were administered intravenously (IV) in 10 hour intervals with the first series of doses administered soon after MRSA injection. All mice in the control groups that received vehicle without peptide (0 mg/kg doses) died within 48 hours.
  • bolus SQ dose and 2.5 x 5 mg/kg IN dosage regimen 75% and 50% of mice survived, respectively, during the course of a fourteen-day study (Figure 28).
  • IP intraperitoneal
  • mice were infected with lethal doses of MRSA (ATCC 33591) (IP left side). Each group of mice was treated with a bolus IP (right side) dose of peptide SEQ HD NO: 8, 12, 17, 18, or 26 at 45-60 min after initial infection. The mice were observed for up to 14 days. All mice in the control group that received vehicle without peptide died within 48 hours. Hi each case, a single dose ofthe appropriate amount of peptide was sufficient to completely protect various groups of mice from MRSA infections ( Figures 6, 24, 25, and 26; Table 12).
  • mice were also infected with lethal doses of VREF (ATCC 51575) (IP left side). Each group of mice was treated with a bolus IP (right side) dose of peptide SEQ HD NO: 12, 17, or 18 at 45-60 min after initial infection. The mice were observed for 14 days. All mice in the control group that received vehicle without peptide died within 48 hours. Hi each case, a single dose ofthe appropriate amount of peptide was sufficient to completely protect various groups of mice from VFEF infections ( Figure 27, Table 12).
  • Table 12 In vivo Protection Doses (PD 5 o) and Lethal Doses (LD 5 o) of cyclic peptides
  • the effective doses were parallel to those required to kill bacteria in vitro.
  • the dosages of peptides having SEQ HD NO:18, 8, 12, 17, and 26 at which 50% of animals are protected from S. aureus MRSA infection (PD50 ) were 8 mg/kg, 7 mg/kg, 20 mg/kg, 7 mg/kg, and 15 mg/kg, respectively.
  • the dosages of peptides having SEQ ID NO.T8, 12 and 17 at which 50% of animals are protected from E. faecium VREF infection (PD 50) were 7 mg/kg, 5 mg/kg and 13 mg/kg, respectively.
  • the trend of these values is similar to the trend ofthe MIC values observed for in vitro antibacterial studies, as shown by Table 13, below.
  • V D (L/kg) 0.58 0.67 0.47
  • EXAMPLE 5 Cyclic ⁇ -Peptides Self-Assemble to Form Transmembrane Ion Channels
  • the observed conductance in 500 mM KCI with peptide concentrations of about 30 mM in the subphase is 56 pS, corresponding to the rates of channel mediated K + transport of 1.9 x 10 7 ions s "1 for both tetrapeptides.
  • Such a transport speed is more than twice that of gramicidin A under similar conditions.
  • FT-IR studies in lipid membranes were also undertaken that provided evidence of transmembrane channels formed by these peptides.
  • Peptide preparations displayed all expected peptide IR signals including amide I, amide II and N-H bands.
  • the observed amide N-H stretching bands at 3289 cm “1 and 3297 cm “1 indicate the existence of tight backbone hydrogen-bonding networks with an average inter-subunit distance of 4.8 A that are consistent with solid state IR data on cyclic D, L- ⁇ -peptides. Therefore, cyclic /3-peptides can also form transmembrane ion channels.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • General Health & Medical Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

La présente invention concerne de nouveaux agents anti-microbiens et des compositions qui incluent des peptides cycliques portant une séquence d'acides aminés faisant alterner les acides aminés L et D. Selon un autre mode de réalisation, les peptides cycliques sont faits d'acides aminés β.
PCT/US2003/014240 2002-05-06 2003-05-06 Peptides anti-microbiens et compositions WO2003093300A2 (fr)

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PCT/US2002/014329 WO2002090503A2 (fr) 2001-05-04 2002-05-06 Peptides antimicrobiens et compositions

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008116194A2 (fr) * 2007-03-22 2008-09-25 Innovative Biologics, Inc. Bloqueurs de facteurs virulents formateurs de pores et leur utilisation comme agents anti-infectieux
US7566765B2 (en) 2000-03-06 2009-07-28 Rigel Pharmaceuticals, Inc. Heterocyclic compounds containing a nine-membered carbon-nitrogen ring
WO2010051667A1 (fr) * 2008-11-10 2010-05-14 复旦大学 Compositions pharmaceutiques comprenant des nanotubes de peptide cyclique et utilisations de celles-ci
US7851457B2 (en) 2004-01-29 2010-12-14 Innovative Biologics, Inc. β-Cyclodextrin derivatives
EP2348039A3 (fr) * 2005-12-22 2011-08-24 Novabiotics Limited Peptides antimicrobiens cycliques
AU2012203804B2 (en) * 2005-12-22 2014-10-16 Novabiotics Limited Cyclic antimicrobial peptides

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995010535A1 (fr) * 1993-10-14 1995-04-20 The Scripps Research Institute Tube peptidique cyclique

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995010535A1 (fr) * 1993-10-14 1995-04-20 The Scripps Research Institute Tube peptidique cyclique

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
FERNANDEZ-LOPEZ, ET AL: 'ANTIBACTERIAL AGENTS BASED ON THE CYCLIC D,L-ALPHA-PEPTIDE ARCHITECTURE' NATURE vol. 412, no. 6845, 26 July 2001, pages 452 - 455, XP002971654 *
GHADLRI, ET AL: 'SELF-ASSEMBLING ORGANIC NANOTUBES BASED ON A CYCLIC PEPTIDE ARCHITECTURE' NATURE vol. 366, 25 November 1993, pages 324 - 327, XP002936460 *
RAPAPORT, ET AL: 'CRYSTALLINE CYCLIC PEPTIDE NANOTUBES AT INTERFACE' J. AM. CHEM. SOC. vol. 121, 1999, pages 1186 - 1191, XP002971655 *

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7566765B2 (en) 2000-03-06 2009-07-28 Rigel Pharmaceuticals, Inc. Heterocyclic compounds containing a nine-membered carbon-nitrogen ring
US7851457B2 (en) 2004-01-29 2010-12-14 Innovative Biologics, Inc. β-Cyclodextrin derivatives
EP2348039A3 (fr) * 2005-12-22 2011-08-24 Novabiotics Limited Peptides antimicrobiens cycliques
EP2357190A3 (fr) * 2005-12-22 2011-08-24 Novabiotics Limited Peptides antimicrobiens cycliques
AU2012203804B2 (en) * 2005-12-22 2014-10-16 Novabiotics Limited Cyclic antimicrobial peptides
WO2008116194A2 (fr) * 2007-03-22 2008-09-25 Innovative Biologics, Inc. Bloqueurs de facteurs virulents formateurs de pores et leur utilisation comme agents anti-infectieux
WO2008116194A3 (fr) * 2007-03-22 2009-02-26 Innovative Biolog Inc Bloqueurs de facteurs virulents formateurs de pores et leur utilisation comme agents anti-infectieux
WO2010051667A1 (fr) * 2008-11-10 2010-05-14 复旦大学 Compositions pharmaceutiques comprenant des nanotubes de peptide cyclique et utilisations de celles-ci

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AU2003228896A8 (en) 2003-11-17
AU2003228896A1 (en) 2003-11-17

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