WO2008061192A2 - Stabilized maml peptides and uses thereof - Google Patents

Abstract

Stably cross-linked a polypeptides related to human MAML are described. These cross-linked polypeptides contain at least two modified amino acids that together form an internal cross-link or tether that can help to stabilize the alpha-helical secondary structure that is thought to be important for binding of MAML peptides to the Notch transcription complex, a complex that includes ICN and CSL.

Description

Stabilized MAML Peptides and Uses Thereof

BACKGROUND

Notch receptors are transmembrane receptors that involved in a variety of important signaling pathways. Mutations in human NOTCH 1 are commonly found in human T cell acute lymphoblastic leukemias (T-ALL) and it is thought that abnoπnalities in Notch signaling are involved in other cancers.

The Notch signaling pathway is complex. When an appropriate ligand binds to Notch a proteolytic event occurs which allows a portion of the Notch receptor called ICN to enter the cell nucleus where is interacts with CSL, a transcription factor that binds DNA, and a protein that is a member of the Mastermind-like

(MAML) family. The assembled complex can active transcription of certain genes. It is known that certain fragments of MAML (e.g., within amino acids 13-74 of human MAML-I) can act to interfere with Notch activation of transcription.

SUMMARY Described below are stably cross-linked a polypeptides related to human

MAML. These cross-linked polypeptides contain at least two modified amino acids that together form an internal cross-link (also referred to as a tether) that can help to stabilize the alpha-helical secondary structure that is thought to be important for binding of M AML peptides to the Notch transcription complex, a complex that includes ICN and CSL. It is thought that the constrained secondary structure can increase resistance of the polypeptide to proteolytic cleavage. Accordingly, a cross- linked polypeptide described herein can have improved biological activity relative to a corresponding polypeptide that is not cross-linked. The cross-linked polypeptides described herein can be used therapeutically, e.g., to treat a variety of cancers in a subject. Inhibitors of Notch function may be useful in reducing unwanted immune responses, undesirable angiogenesis, treatment of human T cell acute lymphoblastic leukemias, treatment of mucoepidermoid carcinomas, treatment of breast cancer, treatment of mcdulloblastoma, and treatment of pancreatic cancer, treatment of lung cancer, treatment of ovarian cancer, treatment of atherosclerosis (e.g., heart disease), treatment of melanoma, treatment of colon cancer, and treatment of cancers that exhibit resistance to gamma secretase inhibitors.

In one aspect, the invention features a modified polypeptide of Formula (I),

Formula (1) wherein; each Ri and R2 are independently H or a Ci to Cio alkyl, alkcnyl, alkynyl, arylalky], cycloalkylalkyl, hctcroarylalkyl, or heterocyclylalkyl; Rj is alkyl, alkenyl, alkynyl; [R₄-K.-R₄],,; each of which is substituted with 0-

6 R₅;

R4 is alkyl, alkenyl, or alkynyl;

R₅ is halo, alkyl, OR₆, N(R₆)₂, SR₆, SOR₆, SO₂R₆, CO₂Re, Re, a fluorescent moiety, or a radioisotope;

K is O, S, SO, SO₂, CO₁ CO₂, CONR₆, or * ^Λ ;

R₆ is H, alkyl, or a therapeutic agent; n is 3, 4 or 6; x is an integer from 2-10; w and y arc independently an integer from 0-100 ( e.g., 1 , 2 3, 4, 5, 6 or 7); 7. is an integer from 1-10 (e.g., 1 , 2, 3, 4, 5, 6, 7, 8, 9, 10); and each Xaa is independently an amino acid, wherein the polypeptide comprises at least 8 (e.g., 8, 9, 10, 11, 12, 13 or more) contiguous amino acids of SEQ ID NO: 1, 2, 3, 4, 5, 6 or 7 except that: (a) within the 8 contiguous amino acids of SEQ ID NO:1, 2, 3, 4, 5, 6 or 7 the side chains of at least one pair of amino acids separated by 3, 4 or 6 amino acids is replaced by the linking group R₃ which connects the alpha carbons of the pair of amino acids as depicted in formula 1; and (b) the alpha carbon of the first of the pair of amino acids is substituted with Ri as depicted in formula I and the alpha carbon of the second of the pair of amino acids is substituted with R₂ as depicted in formula I or a pharmaceutically acceptable salt thereof.

SEQ ID NO: 1 is a sequence created from an alignment of human MΛML- 1 , 2, and 3, starting at amino acid 19 of MAML-I and extending to amino acid 61. SEQ ID NOs:2 - 4 respectively are the amino acid sequences of MAML-1 , 2 and 3 over this same region. SEQ ID NOs:5 - 7 respectively are the amino acid sequences of MAML-1 , 2 and 3 over a somewhat larger region.

Hisi Scτ2 Xaa3 Xaa_t Xaas Glue Arg₇ Leu« Argg Xaajo Xaai i He^ Xaao Xaau Cysis Argi₆ Xaa_π Hisjg His_i9 Xaa₂o Xaa₂ι Cys22 GIU₂3 Xaa₂₄ Arg∑s Tyr₂6 Xaa₂7 Xaa₂g Xaa₂<>

Xaajo Xaaji GIU3₂ Xaa₃₃ Xaa₃₄ Xaa₃s Xaa3β GIU3₇ Arg₃8 Xaa₃9 Xaa₄o TlIr_4I Xaa4₂ Xaa^

LeIL₄₄ Xaa₄5 Xaa^ Xaa₄₇ (SEQ ID NO:1), wherein

Xaa₃ is Ala or Thr;

Xaa₄ is Via or lie; Xaas is Met or VaI;

Xaaio is Arg, Ala, or GIn

Xaai3 is GIu or Ala

Xaa_i4 is Leu, VaI or GIy

Xaa^o is Ser, Leu or VaI

Xaa₂i is Thr, Scr or Asn

Xaa₂₄ is Arg, GIy or Asn

Xaa₂7 is GIu or GIn

Xaa₂₈ is Ala, Arg or GIn Xaa₂₉ is VaI, GIy or Ala

Xaa3o is Ser, Arg or GIn

Xaa₃₃ Arg, Ser or GIn

Xaa₃₄ Leu or Ser Xaa₃s is GIu or Asp

Xaa₃9 is GIn GIu or Arg

Asp Xaa₄₂ is Phc, Leu or VaI Xa&}₃ is Λla, Gin or Scr Xaa^ is His, Leu or Tyr

Ser Xaa»7 is Arg or Leu

Within SEQ ID NO:1 , the following pairs of amino acid can be cross-linked: 2/9, 6/13, 13/17, 17/20, 20/27, 20/24, 35/39, 39/46, and 39/43. The corresponding residues in SEQ ID NOs:2-8 can be cross-linked.

SEQ ID NO:2 (MAML-I ; amino acids 19-62): VMERLRRRIELCRRHHSTCEARYEA VSPERLELEROHTFALHQR

SEQ ID NO:3 (MAML-2):

IVERLRARIA VCROHHLSCEGRYERGRAESSDRERESTLOLLSL

SEQ ID NO:4 (MAML-3):

VVERLRORIEGCRRHHVNCENRYOOAOVEOLELERRDTVSLYOR

SEQ ID NO:5 (MAML-I ; includes predicted domain for binding the transcription complex):

HSAVMERLRRRIELCRRHHSTCEARYEΛVSPERLELERQHTFALHQRCIQAK

AKRAGKH

SEQ ID NO:6 (MAML-2; includes predicted domain for binding the transcription complex):

HSAIVERLRARIA VCRQHHLSCEGRYERGRAESSDRERESTLQLLSLVQHGQ

GARKAGKH

SEQ ID NO:7 (MAML-3; includes predicted domain for binding the transcription complex): AVPKHSTVVERLRQRIEGCRRHHVNCENRYQQAQVEQLFXERRDTVSLYQR TLEQRAKKS

SEQ ID NO:8 (MAML-I core) ERLRRRIELCRRHHST

SEQ ID NO:9 (MAML-2 core) ERLRAR1AVCRQHHLSC

SEQ ID NO: 10 (M AML-3 core) ERLRQRIEGCRRHHVN

In some instances, the modified polypeptide binds a complex of ICN and CSL, e.g., ICN and CSL bound to DNA. In some instances, each y is independently an integer between 3 and 15.

In some instances each y is independently an integer between 1 and 15.

In some instances, Ri and Ri are each independently H or Ci-C_δ alkyl.

In some instances, Ri and R₂ are each independently Ci-Cj alkyl.

In some instances, at least one of Ri and R₂ arc methyl. For example Ri and R₂ arc both methyl.

In some instances R3 is alkyl (e.g., Cg alkyl) and x is 3.

In some instances, R₃ is Ci ₁ alkyl and x is 6.

In some instances, R₃ is alkenyl (e.g., Cg alkenyl) and x is 3.

In some instances x is 6 and Rj is Cu alkenyl. In some instances, R₃ is a straight chain alkyl, alkenyl, or alkynyl.

In some instances R₃ is -CH₂-CH₂-CH₂-CH=CH-CH₂-CH₂-CHr.

In certain embodiments the two alpha, alpha disubstitutcd stereocenters (alpha carbons) are both in the R configuration or S configuration (e.g., i, i+4 crosslink), or one stcreocentcr is R and the other is S (e.g., i, i+7 cross-link). Thus, where Formula I is depicted as

the C and C" disubstituted stereocenters can both be in the R configuration or they can both be in the S configuration, for example when x is 3. When x is 6, the C disubstituted stereocenter is in the R configuration and the C" disubstituted stereocenter is in the S configuration. The R₃ double bond may be in the E or Z stereochemical configuration.

In some instances R₃ is [R₄-K-R^_n; and R₄ is a straight chain alkyl, alkenyl, or alkynyl. In some instances, the polypeptide includes an amino acid sequence which is at least about 60% (70%, 80%, 85%, 90%, 95% or 98%) identical to the amino acid sequence of

HSAVMERLRRRIELCRRHHSTCEARYEA VSPERLELERQHTFALHQRCIQAK AKR (SEQ ID NO: 8). In some instances the modified polypeptide comprises at least 8 contiguous amino acids of

HSAVMERLRRRIELCRRHHSTCEARYEAVSPERLELERQHTFALHQRCIQAK AKR (SEQ ID NO:8). except that at least one pair of amino acids within the 8 (e.g., 8, 9, 10, 1 1 , 12, 13 or more) contiguous amino acids are replaced by modified amino acids that can form an internal cross-link. The tether can include an alkyl, alkenyl, or alkynyl moiety (e.g., C5, Cs or

Ci ₁ alkyl or a Cj, Q or C) ₁ alkenyl, or C5, C₈ or Ci ₁ alkynyl). The tethered amino acid can be alpha disubstituted (e.g., C₁-C3 or methyl). [Xaa]_y and [Xaa]_w are peptides that can independently comprise at least 1 , 2 3, 4, 5, 6, 7, 8, 9, 10, 1 1 , 12, 13, 14, 15, 16, 17, 18, 19, 20, 25 or more contiguous amino acids of a MAML polypeptide and [Xaa]_x is a peptide that can comprise 3 or 6 contiguous amino acids of acids of a MAML peptide.

The polypeptide can comprise 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50 amino acids of a MAML polypeptide (e.g., human MAML-I , 2 or 3 or a consensus MAML polypeptide). The amino acids are contiguous except that one or more pairs of amino acids separated by 3 or 6 amino acids arc replaced by amino acid substitutes that form a cross-link, e.g., via R₃. Thus, at least two amino acids can be replaced by tethered amino acids or tethered amino acid substitutes. Thus, where formula I is depicted as

[Xaa]_y and [Xaa]_y- can each comprise contiguous polypeptide sequences from the same or different MAML peptides.

Jn some instances the polypeptide comprises an amino acid sequence selected from SEQ ID NOs:8, 9 and 10 wherein: (a) the side chains of amino acids 8 and 12 arc replaced by the linking group R₃ which connects the alpha carbons of amino acids 8 and 12 as depicted in formula 1; and (b) the alpha carbon of amino acid 8 is substituted with Ri as depicted in formula I and the alpha carbon of amino acid 12 is substituted with R₂ as depicted in formula I. The invention features cross-linked polypeptides comprising at least 8 (e.g.,

8, 9, 10, 1 1 , 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 30, 35, 40, 45, 50 or more) contiguous amino acids of a MAML polypeptide wherein the alpha carbons of two amino acids that are separated by three amino acids (or six amino acids) are linked via R3, one of the two alpha carbons is substituted by Ri and the other is substituted by R₂ and each is linked via peptide bonds to additional amino acids.

In some embodiments the polypeptide acts as dominant negative inhibitor of Notch.

In some instances, the polypeptide also includes a fluorescent moiety or radioisotope. In some instances, Ri and R₂ arc methyl; R₃ is C» alkyl, Ci ₁ alkyl, C« alkenyl,

Cn alkenyl, C» alkynyl, or Cu alkynyl; and x is 2, 3, or 6.

In some instances, the polypeptide includes an PEG, tat protein, affinity label, a targeting moiety, and/or a biotin moiety. In another aspect, the invention features a method of making a polypeptide of Formula (III), including providing a polypeptide of Formula (II); and

Formula (II) treating the compound of Formula (II) with a catalyst to promote a ring closing metathesis, thereby providing a compound of formula (III)

Formula (III) wherein each R i and R₂ are independently H, alky], alkenyl, alkynyl, arylalkyl, cycloalkylalkyl; heteroarylalkyl; or heterocyclylalkyl; each n is independently an integer from 1-15; x is 2, 3, or 6 w and y are independently an integer from 0-100; z is an integer from 1 -10 (e.g., 1 , 2, 3, 4, 5, 6, 7, 8, 9, 10); and each Xaa is independently an amino acid;

In some instances, the polypeptide binds to a complex of ICN and CSL. In some instances, the catalyst is a ruthenium catalyst. In some instances, the method also includes providing a reducing or oxidizing agent subsequent to the ring closing metathesis.

In some instances, the reducing agent is H₂ or the oxidizing agent is osmium tetroxidc

In some instances, the invention features a method of treating a subject including administering to the subject any of the compounds described herein. In some instances, the method also includes administering an additional therapeutic agent.

In some instances, the invention features a method of treating cancer in a subject including administering to the subject any of the compounds described herein. In some instances, the method also includes administering an additional therapeutic agent.

In some instances, the invention features a library of the compounds described herein.

Combinations of substituents and variables envisioned by this invention are only those that result in the formation of stable compounds. The term "stable", as used herein, refers to compounds which possess stability sufficient to allow manufacture and which maintains the integrity of the compound for a sufficient period of time to be useful for the purposes detailed herein (e.g., therapeutic administration to a subject or generation of reagents to study or discover a biological pathway cither in vitro or in vivo).

The compounds of this invention may contain one or more asymmetric centers and thus occur as racemates and racemic mixtures, single enantiomers, individual diastcreomers and diastercomcric mixtures. All such isomeric forms of these compounds are expressly included in the present invention. The compounds of this invention may also be represented in multiple tautomeric forms, in such instances, the invention expressly includes all tautomeric forms of the compounds described herein (e.g., alkylation of a ring system may result in alkylation at multiple sites, the invention expressly includes all such reaction products). All such isomeric forms of such compounds are expressly included in the present invention. All crystal forms of the compounds described herein are expressly included in the present invention.

The teπn "amino acid" refers to a molecule containing both an amino group and a carboxyl group. Suitable amino acids include, without limitation, both the D- and L- isomers of the 20 common naturally occurring amino acids found in peptides (e.g., A, R, N, C, D, Q, E, G, H, I, L, K, M, F, P, S, T, W, Y, V (as known by the one letter abbreviations)) as well as the naturally occurring and unnaturally occurring amino acids prepared by organic synthesis or other metabolic routes. The tabic below provides the structures of the side chains for each of the 20 common naturally-occurring amino acids. In this table the "-" at right side of each structure is the bond to the alpha carbon.

A "non-essential" amino acid residue is a residue that can be altered from the wild-type sequence of a polypeptide (without abolishing or substantially altering its activity. An "essential" amino acid residue is a residue that, when altered from the wild-type sequence of the polypeptide, results in abolishing or substantially abolishing the polypeptide activity.

A "conservative amino acid substitution" is one in which the amino acid residue is replaced with an amino acid residue having a similar side chain. Families of amino acid residues having similar side chains have been defined in the art. These families include amino acids with basic side chains (e.g., lysine, arginine, histidine), acidic side chains (e.g., aspartic acid, glutamic acid), uncharged polar side chains (e.g., glycine, asparagine, glutamine, serine, threonine, tyrosine, cysteine), nonpolar side chains (e.g., alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine, tryptophan), beta-branched side chains (e.g., threonine, valine, isoleucine) and aromatic side chains (e.g., tyrosine, phenylalanine, tryptophan, histidine). Thus, a predicted nonessential amino acid residue in a MAML polypeptide, for example, is preferably replaced with another amino acid residue from the same side chain family.

The symbol " ^ "when used as part of a molecular structure refers to a single bond or a trans or cis double bond.

The term "amino acid side chain" refers to a moiety attached to the α-carbon in an amino acids. For example, the amino acid side chain for alanine is methyl, the amino acid side chain for phenylalanine is phenylmethyl, the amino acid side chain for cysteine is thiomcthyl, the amino acid side chain for aspartate is carboxymcthyl, the amino acid side chain for tyrosine is 4-hydroxyphcnylmethyl, etc. Other non- naturally occurring amino acid side chains are also included, for example, those that occur in nature (e.g., an amino acid metabolite) or those that are made synthetically (e.g., an alpha di-substitutcd amino acid).

The term polypeptide encompasses two or more naturally occurring or synthetic amino acids linked by a covalcnt bond (e.g., a amide bond). Polypeptides as described herein include full length proteins (e.g., fully processed proteins) as well as shorter amino acids sequences (e.g., fragments of naturally occurring proteins or synthetic polypeptide fragments).

The term "halo" refers to any radical of fluorine, chlorine, bromine or iodine. The term "alkyl" refers to a hydrocarbon chain that may be a straight chain or branched chain, containing the indicated number of carbon atoms. For example, Ci- Cio indicates that the group may have from 1 to 10 (inclusive) carbon atoms in it. In the absence of any numerical designation, "alkyl" is a chain (straight or branched) having 1 to 20 (inclusive) carbon atoms in it. The term "alkylene" refers to a divalent alkyl (i.e., -R-). The term "alkenyl" refers to a hydrocarbon chain that may be a straight chain or branched chain having one or more carbon-carbon double bonds. The alkenyl moiety contains the indicated number of carbon atoms. For example, C₂-C₁₀ indicates that the group may have from 2 to 10 (inclusive) carbon atoms in it. The term "lower alkenyl" refers to a Ci-Cg alkenyl chain. In the absence of any numerical designation, "alkenyl" is a chain (straight or branched) having 2 to 20 (inclusive) carbon atoms in it.

The term "alkynyl" refers to a hydrocarbon chain that may be a straight chain or branched chain having one or more carbon-carbon triple bonds. The alkynyl moiety contains the indicated number of carbon atoms. For example, C₂-C₁0 indicates that the group may have from 2 to 10 (inclusive) carbon atoms in it. The term "lower alkynyl" refers to a C_Ϊ-C_S alkynyl chain. In the absence of any numerical designation, "alkynyl" is a chain (straight or branched) having 2 to 20 (inclusive) carbon atoms in it. 'lTic term "aryl" refers to a 6-carbon monocyclic or 10-carbon bicyclic aromatic ring system wherein 0, 1, 2, 3, or 4 atoms of each ring may be substituted by a substitucnt. Examples of aryl groups include phenyl, naphthyl and the like. The term "arylalkyl" or the term "aralkyl" refers to alkyl substituted with an aryl. The teπn "arylalkoxy" refers to an alkoxy substituted with aryl. The term "cycloalkyl" as employed herein includes saturated and partially unsaturated cyclic hydrocarbon groups having 3 to 12 carbons, preferably 3 to 8 carbons, and more preferably 3 to 6 carbons, wherein the cycloalkyl group additionally may be optionally substituted. Preferred cycloalkyl groups include, without limitation, cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohcxyl, cyclohcxcnyl, cycloheptyl, and cyclooctyl.

The term "heteroaryl" refers to an aromatic 5-8 membered monocyclic, 8-12 mcmbcrcd bicyclic, or 11-14 membered tricyclic ring system having 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S (e.g., carbon atoms and 1-3, 1-6, or 1-9 heteroatoms of N, O, or S if monocyclic, bicyclic, or tricyclic, respectively), wherein 0, 1 , 2, 3, or 4 atoms of each ring may be substituted by a substituent. Examples of heteroaryl groups include pyridyl, furyl or furanyl. imidazolyl, benzimidazolyl, pyrimidinyl, thiophenyl or thienyl, quinolinyl, indolyl, thiazolyl, and the like. The term "heteroarylalkyl" or the term "heteroaralkyl" refers to an alkyl substituted with a heteroaryl. The term "heteroarylalkoxy" refers to an alkoxy substituted with heteroaryi. The term "hetcrocyclyl" refers to a nonaromatic 5-8 membered monocyclic,

8-12 membered bicyclic, or 11 - 14 membered tricyclic ring system having 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1 -9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S (e.g., carbon atoms and 1-3, 1 -6, or 1-9 heteroatoms of N, O, or S if monocyclic, bicyclic, or tricyclic, respectively), wherein 0, 1, 2 or 3 atoms of each ring may be substituted by a substituent. Examples of hetcrocyclyl groups include piperazinyl, pyrrolidinyl, dioxanyl, morpholinyl, tetrahydrofuranyl, and the like.

The term "substituents" refers to a group "substituted" on an alkyl, cycloalkyl, aryl, hetcrocyclyl, or heteroaryl group at any atom of that group. Suitable substituents include, without limitation, halo, hydroxy, mcrcapto, oxo, nitro, haloalkyl, alkyl, alkaryl, aryl, aralkyl, alkoxy, thioalkoxy, aryloxy, amino, alkoxycarbonyl, amido, carboxy, alkancsulfonyl, alkylcarbonyl, and cyano groups. The details of one or more embodiments of the invention are set forth in the accompanying drawings and the description below. Other features, objects, and advantages of the invention will be apparent from the description and drawings, and from the claims.

DESCRIPTION OF DRAWINGS

FlG 1 depicts MAML polypeptides and locations for modification

FIG 2 depicts a synthetic strategy for the generation of α,odisubstituted non-natural amino acids containing olefinic side chains.

FIG 3 depicts certain MAML polypeptides used in studies described herein.

FlG 4 depicts a stapled MAML polypeptide.

FIG. 5 depicts a CD spectra of a stapled polypeptide.

FIG 6 depicts stapled MAML polypeptides. FIG 7 depicts the results of surface plasmon resonance showing that

BioSAHNl 1 binds ICN in a dose dependent manner. FIG 7 depicts the results of surface plasmon resonance showing that immobilized ICN associates with CSL in a dose-dependent manner.

FIG. 9 depicts the results of studies examining the binding of immobilized stapled and unstapled SAHNl 1 to ICNl . FIG. 10 depicts the results of studies on cellular uptake of SAHNl , SAHN2 and SΛHN6.

FIG. 1 1 depicts the results of studies on cellular uptake of stapled and unstapled SAHNl .

FlG. 12 depicts the results of a study showing that stapled SAHN 1 1 reduces expression of the CSL-responsive reporter in a dose-depcndcnt manner.

FIG. 13 depicts the results of a study showing that T-ALLl cells exposed to either SAHN 11 -FlTC or SAHNl-FITC exhibit reduced HESl expression relative to expression of a housekeeping gene.

FlG. 14 depicts the results of a study showing that stapled SAHN2 reduces the viability of MOLT4 cells.

FIG. 15 depicts the results of a study showing that stapled SAHNl, but not unstapled SAHN l , reduces the viability of ALL-SIL cells.

FIG. 16 depicts the results of a study showing that stapled SAHN 1, but not unstapled SAHNl , reduces the viability of KOPTKl cells. FlG. 17 depicts the results of a study showing that stapled SAHN 11 reduces the viability of MOLT4 cells.

FlG. 18 depicts the results of a study showing that stapled SAHNl 1 reduces the viability of TALLl cells.

FIG. 19 depicts the results of a study showing that SAHNl , but not SAHN l- D can bind to ICN 1 /CSL in T-ALL cellular lysates.

FlG. 20 depicts the results of a study showing that SAHNl can compete off ICN l bound to MAML in T-ALL cellular lysates.

FIG. 21 depicts the results of a study showing that SAHN l -D cannot compete off ICNl bound to MAML in T-ALL cellular lysates FIG. 22 depicts the results of a study showing that SAHN 1 and SAHN 1 1 can cause a decrease in transcription from a CSL-responsive reporter in T-ALL cells. FIG. 23 depicts the results of a study showing that SAHNl , but not SANNl- D n cause a decrease in transcription from a CSL-responsive endogenous genes in T- ALL cells.

FlG. 24 depicts the results of a study showing that SAHNl can elicit an apoptotic response in T-ALL cells.

FIG. 25 depicts the results of a study showing that SAHNl decreases the viability of MOLT4 T-ALL cells.

DETAILED DESCRIPTION

Described herein arc internally cross-linked alpha helical domain polypeptides related to human MAML. The polypeptides include a tether between two non-natural amino acids, which tether significantly enhances the alpha helical secondary structure of the polypeptide. Generally, the tether or cross-link

(sometimes referred to as staple) extends across the length of one or two helical turns (i.e., about 3.4 or about 7 amino acids). Accordingly, amino acids positioned at i and i+3; i and i+4; or i and i+7 are ideal candidates for chemical modification and cross-linking. Thus, for example, where a peptide has the sequence ...Xaai, Xaai, Xaa.i, Xa&j, Xaas, Xa&β, Xaa7, Xaa₈, Xaa$... (wherein "..." indicates the optional presence of additional amino acids), cross-links between Xaai andXaa}, or between Xaai and Xaas, or between Xaai andXaag are useful as are cross-links between Xaai and Xaas, or between Xaa? and Xaa6, or between Xaa_∑ and Xaa9, etc. The polypeptides can include more than one crosslink within the polypeptide sequence to cither further stabilize the sequence or facilitate the stabilization of longer polypeptide stretches. If the polypeptides are too long to be readily synthesized in one part, independently synthesized cross-linked peptides can be conjoined by a technique called native chemical ligation (Bang, et al., J. Am. Chem Soc. 126:1377). The novel cross-linked polypeptides are useful, for example, to mimic or study proteins or polypeptides having one or more alpha-helical domains.

Analysis conserved residues among MAML-I, 2 and 3; analysis of the predicted interaction between MAML and Notch; and analysis of predicted alpha- helical regions led to the identification amino acids that might be replaced to provide a cross-link without significantly inhibiting binding to Notch. Thus, as shown in FIG 2 for MAML-I, residues that might be cross-linked are doubled underlined. Substitutions can be made at discrete locations, namely the "i, and i+4 positions" or the "i, and i+7 positions" shown for each phase (1 to 6) which facilitate cross- linking chemistry by placing reactive residues on the same face of the α-helix.

Highly conserved amino acids among MAML polypeptides and those thought be important in protein-protein interactions based on X-ray crystallographic, are preferably not replaced. In FIG. 2 residues where changes are expected to be tolerated are single underlined. In certain circumstances, conserved amino acids can be replaced by other amino acids (e.g., synthetic non-naturally occurring amino acids). α,α-Disubstituted non-natural amino acids containing olefinic side chains of varying length can synthesized by known methods (Williams et al. 1991 / Am. Chem. Soc. 1 13 :9276; Schafmeister et al. 2000 J. Am. Chem Soc. 122:5891 ). FlG. 2 is a schematic depiction of the preparation of the non-natural amino acid (Fmoc- S5) used in solid phase peptide synthesis (SPPS) of i linked to i+4 peptides (one turn of the alpha helix is stabilized). For peptides where an i linked to i+7 staple is used (two turns of the helix stabilized) one S5 amino acid is used and one R8 is used. R8 is synthesized using the same route, except that the starting chiral auxiliary confers the R-alkyl-stcreoisomer. Also, 8-iodooctene is used in place of 5- iodopentenc. Inhibitors are synthesized on a solid support using solid-phase peptide synthesis (SPPS) on MBHA resin. Non-natural amino acids were synthesized by Moellering for incorporation into the final peptide product.

Various internally cross-linked peptides (REM-Gl to REM-Gl 3, also called SAHNl to SAHN 13, respectively) shown in FIG. 3 were produced (X is a modified amino acid forming a cross-link). The underlined portions indicate the extent of each polypeptide, and the remainder of the MAML-I sequence in each case is provided for context.

FIG. 4 is a schematic drawing and detailed structural depiction of a modified polypeptide having the sequence of REM-Gl (SAHNl). As seen in the circular dichromism spectra of FlG. 5, the modified polypeptide can be 96% alpha helical as compared to 40% when not cross-linked. FIG. 6 shows the detailed structure of versions of the modified, internally cross-linked polypeptide REM-Gl 1 (SAHN l 1 ) that include either biotin or FITC labels.

Surface plasmon resonance was used to demonstrated that the biotin-iabcled cross-linker version of REM-Gl 1 (BioSAHNl 1) binds ICN in a dose dependent manner (FIG. 7).

Biochemical association between stapled peptides and the Notch complex was also investigated using surface plasmon resonance. These studies employed immobilized ICN protein (an anti-GST antibody and a GST-tagged, purified ICN protein comprising the RAM and ANK domains). Other studies employed biotinylatcd stapled peptides and a streptavidin-functionalized sensor surface.

We demonstrated that immobilized ICN associates with CSL in a dose- dependent manner. The association exhibited a two-phase kinetic association, first with RAM binding and subsequently with a lower-affinity association with the ANK domain (sec FIG. 8). Non-specific binding to a reference surface with anti-GST antibody was only minimal.

Binding of immobilized stapled and unstapled SAHNl 1 to ICNl demonstrated that stapled (cross-linked) SAHNl 1 binds ICN with greater affinity (Kd = 0.96 μM) than non-stapled SAHNl 1 (Kd = 2.63 μM) (FlG. 9). Immunoprecipitation studies using MOLT4 cell lysates, ALL-SIL cell lysates and KOPTKl cell lysates found that biotin labeled SAHNl can be used to pull down ICN. A reverse immunoprecipitation assay using FITC labeled SAHN l found that SAHN l can be used to pull down ICN in MOLT4 cell lysates.

Automated quantitative immunofluorescence was used to determine the intracellular distribution of fluorophore-labeled stapled alpha helices. Cells were incubated with FITC-conjugatcd peptides SAHN 1 , SAHN2, or SAHN6; or control. At 16 hours measurements of cellular fluorescence were taken using epifluorescence microscopy. The results of these studies are shown in FIG. 10 in which each circle represents an individual cell and each column represents a treatment condition. Both SΛHN1 and SAHN2 exhibited significant intracellular passage, whereas SAHN6 did not. Automated quantitative immunofluorescence was also used to determine the intracellular distribution of fluorophorc-labeled stapled alpha helices. Cells were incubated with FITC-conjugatcd peptides SAHN 1 , or unstapled SAHNl . As shown in FlG. 11 , stapling of the peptide did not, in this instance, appear to impact intracellular passage. Epifluoresccnce microscopy demonstrated that SAHNl I exhibits intracellular distribution. Confocal microscopy analysis suggested that both stapled and unstapled SAHNl peptides appear to distribute to the intracellular compartment through endocytosis.

MOLT4 cells transfccted with a CSL-responsive reporter were used to test whether stapled SAHNl 1 can interfere with Notch-mediated activation of transcription. As can be seen in FIG. 12, stapled SAHNl 1 reduced expression of the CSL-responsive reporter in a dose-dependent manner.

HESl is Notch responsive gene. As shown in FIG. 13, T-ALLl cells exposed to cither SAHNl 1-FITC or SAHNl -FITC exhibit reduced HESl expression relative to expression of a housekeeping gene (beta-actin).

As shown in FIG. 14, stapled SAHN2 reduced the viability of MOLT4 cells. As shown in FIG. 15, stapled SAHNl, but not unstapled SAHNl, reduced the viability of ALL-SIL cells. As shown in FIG. 16, stapled SAHNl, but not unstapled SAHNl, reduced the viability of KOPTKl cells. As shown in FIG. 17, stapled SAHN 1 1 reduced the viability of M0LT4 cells. As shown in FIG. 18, stapled SAHNl 1 reduced the viability of TALLl cells.

Immobilized SAHNl was used to measure the apparent Kd for a prc- assembled ICN-CSL complex by surface plasmon resonance. The result of this analysis revealed an apparent Kd of 98 nM. (1 DON'T THINK THERE IS ANY NEED TO SHOW SLIDE 8)

A damaged variant of SAHNl was created by changing the GIu indicated by * in the SAHNl depicted in FIG. 6 to an Arg and changing the Arg indicated by + in the SAIiN l depicted in FIG. 6 to GIu. This damaged variant, which has the same net charge as SANNl, is referred to as SAHN l-D.

Immobilized SAHN l-D was used to measure the apparent Kd for a pre- assembled ICN-CSL complex by surface plasmon resonance. The result of this analysis revealed an apparent Kd of 1.40 μM. (I DON'T THINK THERE IS ANY NEED TO SHOW SLIDE 10)

Immunoprecipitatioii studies using T-ALL (KOPTKl) cell lysatcs demonstrated that SAHN l and SAHN l 1, but not SAHNl-D, can pull down both ICN and CSL. The results of the analysis are shown in FIG. 19. A study using T-ALL cellular lysates found that SAHNl can compete away

ICNl that is bound to immunoprccipitated MAML. The results of this analysis are shown in FIG 20.

A study using T-ALL cellular lysatcs found that SAHNl -D cannot effectively compete away ICNl that is bound to immunoprecipitated MAML. The results of this analysis are shown in FIG 21.

T-ALL cells (MOLT4) harboring a beta-lactamase gene under the control of a CSL responsive promoter was used to study the effect of SAHN l and SAHNl 1 on Notch complex mediated transcription. This study found that both SAHNl and SAHNl 1 decreased transcription and that the decrease was similar in magnitude to that caused by an RNAi directed against Notch and an RNAi directed against lactamase. The results of this analysis are shown in FIG. 22.

A study in T-ALL cells (MOLT4) found that SAHNl, but not SAHNl-D, decrease expression of HES l and HEYl, both Notch-driven genes, in a dose dependent manner. The results of this analysis are show in FIG. 23. A study in gamma secretase resistant T-ALL cells (MOLT4) found that

SAHN 1, but not SAHN 1 -D induces an apoptotic response after 24 or 48 hours. The results of this analysis are show in FlG. 24.

A study in T-ALL cells (KOPTKl) found that SAHN l decreased cell viability (IC₅₀ = 8 μM). SAHN 1 -D had little effect on cell viability. The results of this analysis are show in FIG. 25.

Additional studies found that SAHNl , but not SAHNl-D, is cytotoxic to neoplastic murine lymphocytes derived from transgenic mice harboring the clinically relevant human Notch mutations (a L to P change at position 1601 and a PEST domain mutation).

Polypeptides

In some instances, the hydrocarbon tethers (i.e., cross links) described herein can be further manipulated. In one instance, a double bond of a hydrocarbon alkenyl tether, (e.g., as synthesized using a ruthenium-catalyzed ring closing metathesis (RCM)) can be oxidized (e.g., via epoxidation or dihydroxylation) to provide one of compounds below.

Either the epoxide moiety or one of the free hydroxyl moieties can be further funclionalized. For example, the epoxide can be treated with a nucleophile, which provides additional functionality that can be used, for example, to attach a tag (e.g., a radioisotope or fluorescent tag). The tag can be used to help direct the compound to a desired location in the body or track the location of the compound in the body. Alternatively, an additional therapeutic agent can be chemically attached to the functionalized tether (e.g., an anti-cancer agent such as rapamycin, vinblastine, taxol, etc.). Such derivitization can alternatively be achieved by synthetic manipulation of the amino or carboxy terminus of the polypeptide or via the amino acid side chain. Other agents can be attached to the functionalized tether, e.g., an agent that facilitates entry of the polypeptide into cells.

While hydrocarbon tethers have been described, other tethers are also envisioned. For example, the tether can include one or more of an ether, thiocthcr, ester, amine, or amide moiety. In some cases, a naturally occurring amino acid side chain can be incorporated into the tether. For example, a tether can be coupled with a functional group such as the hydroxyl in serine, the thiol in cysteine, the primary amine in lysine, the acid in aspartate or glutamate, or the amide in asparaginc or glutaminc. Accordingly, it is possible to create a tether using naturally occurring amino acids rather than using a tether that is made by coupling two non-naturally occurring amino acids. It is also possible to use a single non-naturally occurring amino acid together with a naturally occurring amino acid.

It is further envisioned that the length of the tether can be varied. For instance, a shorter length of tether can be used where it is desirable to provide a relatively high degree of constraint on the secondary alpha-helical structure, whereas, in some instances, it is desirable to provide less constraint on the secondary alpha-helical structure, and thus a longer tether may be desired.

Additionally, while examples of tethers spanning from amino acids i to i+3, i to i+4; and i to i+7 have been described in order to provide a tether that is primarily on a single face of the alpha helix, the tethers can be synthesized to span any combinations of numbers of amino acids.

In some instances, alpha disubstituted amino acids are used in the polypeptide to improve the stability of the alpha helical secondary structure. However, alpha disubstituted amino acids are not required, and instances using mono-alpha substituents (e.g., in the tethered amino acids) are also envisioned.

As can be appreciated by the skilled artisan, methods of synthesizing the compounds of the described herein will be evident to those of ordinary skill in the art. Additionally, the various synthetic steps may be performed in an alternate sequence or order to give the desired compounds. Synthetic chemistry transformations and protecting group methodologies (protection and deprotection) useful in synthesizing the compounds described herein are known in the art and include, for example, those such as described in R. Larock, Comprehensive Organic Transformations, VCH Publishers (1989); T.W. Greene and P.G.M. Wuts, Protective Groups in Organic Synthesis, 2d. Ed., John Wiley and Sons (1991); L. Fieser and M. Fieser, Fieser and Ficscr's Reagents for Organic Synthesis, John

Wiley and Sons (1994); and L. Paquette, ed., Encyclopedia of Reagents for Organic Synthesis, John Wiley and Sons (1995), and subsequent editions thereof.

The peptides of this invention can be made by chemical synthesis methods, which are well known to the ordinarily skilled artisan. See, for example, Fields et al., Chapter 3 in Synthetic Peptides: A User's Guide, cd. Grant, W. H. Freeman & Co., New York, N.Y., 1992, p. 77. Hence, peptides can be synthesized using the automated Merrifϊeld techniques of solid phase synthesis with the 0NH₂ protected by either t-Boc or F-moc chemistry using side chain protected amino acids on, tor example, an Applied Biosystcms Peptide Synthesizer Model 430A or 431.

One manner of making of the peptides described herein is using solid phase peptide synthesis (SPPS). The C-tcrminal amino acid is attached to a cross-linked polystyrene resin via an acid labile bond with a linker molecule. This resin is insoluble in the solvents used for synthesis, making it relatively simple and fast to wash away excess reagents and by-products. The N-terminus is protected with the Fmoc group, which is stable in acid, but removable by base. Any side chain functional groups are protected with base stable, acid labile groups. Longer peptides could be made by conjoining individual synthetic peptides using native chemical ligation. Alternatively, the longer synthetic peptides can be synthesized by well known recombinant DNA techniques. Such techniques are provided in well-known standard manuals with detailed protocols. To construct a gene encoding a peptide of this invention, the amino acid sequence is reverse translated to obtain a nucleic acid sequence encoding the amino acid sequence, preferably with codons that are optimum for the organism in which the gene is to be expressed. Next, a synthetic gene is made, typically by synthesizing oligonucleotides which encode the peptide and any regulatory elements, if necessary. The synthetic gene is inserted in a suitable cloning vector and transfected into a host cell. The peptide is then expressed under suitable conditions appropriate for the selected expression system and host. The peptide is purified and characterized by standard methods.

The peptides can be made in a high-throughput, combinatorial fashion, e.g., using a high-throughput multiple channel combinatorial synthesizer available from Advanced Chemtech. In the modified polypeptides one or more conventional peptide bonds replaced by an a different bond that may increase the stability of the polypeptide in the body. Peptide bonds can be replaced by: a relro-invcrso bonds (C(O)-NH); a reduced amide bond (NH-CH₂); a thiomethylene bond (S-CH₂ or CH₂-S); an oxomethylene bond (0-CH₂ or CHi-O); an ethylene bond (CH₂-CH₂); a thioamide bond (C(S)-NH); a trans-olefine bond (CH=CH); an fluoro substituted trans-olefmc bond

(CF=CH); a ketomethylene bond (C(O)-CHR) or CHR-C(O) wherein R is H or CH₃; and a fluoro-kelomethylene bond (C(O)-CFR or CFR-C(O) wherein R is H or F or CH₃. The polypeptides can be further modified by: acetylation, amidation, biotinylation, cinnamoylation, faraesylation, formylation, myristoylation, palmitoylation, phosphorylation (Ser, Tyr or Thr), stearoylation, succinylation and sulfurylation. The polypeptides of the invention may also be conjugated to, for example, polyethylene glycol (PEG); alkyl groups (e.g., C1-C20 straight or branched alkyl groups); fatty acid radicals; and combinations thereof.

Methods of Treatment

The present invention provides for both prophylactic and therapeutic methods of treating a subject at risk of (or susceptible to) a disorder or having a disorder associated with aberrant (e.g., excessive) Notch activity. This is because the polypeptides are expected to act as dominant negative inhibitors of Notch activity. As used herein, the term "treatment" is defined as the application or administration of a therapeutic agent to a patient, or application or administration of a therapeutic agent to an isolated tissue or cell line from a patient, who has a disease, a symptom of disease or a predisposition toward a disease, with the purpose to cure, heal, alleviate, relieve, alter, remedy, ameliorate, improve or affect the disease, the symptoms of disease or the predisposition toward disease. A therapeutic agent includes, but is not limited to, small molecules, peptides, antibodies, ribozymes and antisense oligonucleotides.

The polypeptides of the invention can be used to treat, prevent, and/or diagnose cancers and neoplastic conditions. As used herein, the teπns "cancer", "hypcrprolifcrative" and "neoplastic" refer to cells having the capacity for autonomous growth, i.e., an abnormal state or condition characterized by rapidly proliferating cell growth. Hyperprolifcrativc and neoplastic disease states may be categorized as pathologic, i.e., characterizing or constituting a disease state, or may be categorized as non-pathologic, i.e., a deviation from normal but not associated with a disease state. The term is meant to include all types of cancerous growths or oncogenic processes, metastatic tissues or malignantly transformed cells, tissues, or organs, irrespective of histopathologic type or stage of invasiveness. "Pathologic hypcrproliferative" cells occur in disease states characterized by malignant tumor growth. Examples of non-pathologic hypcrproliferative cells include proliferation of cells associated with wound repair.

Examples of cellular proliferative and/or differentiative disorders include cancer, e.g., carcinoma, sarcoma, or metastatic disorders. The compounds (i.e., polypeptides) can act as novel therapeutic agents for controlling breast cancer, T cell cancers and B cell cancer. The polypeptides may also be useful for treating mucocpidermoid carcinoma and medulloblastoma.

Examples of proliferative disorders include hematopoietic neoplastic disorders. As used herein, the term "hematopoietic neoplastic disorders" includes diseases involving hyperplastic/neoplastic cells of hematopoietic origin, e.g., arising from myeloid, lymphoid or erythroid lineages, or precursor cells thereof. Exemplary disorders include: acute leukemias, e.g., erythroblastic leukemia and acute mcgakaryoblastic leukemia. Additional exemplary myeloid disorders include, but are not limited to, acute promyeloid leukemia (APML), acute myelogenous leukemia (AML) and chronic myelogenous leukemia (CML) (reviewed in Vaickus, L. (1991) Crit Rev. in Oncol./Hcmotol. 11:267-97); lymphoid malignancies include, but are not limited to acute lymphoblastic leukemia (ALL) which includes B- lineage ALL and T-lincage ALL, chronic lymphocytic leukemia (CLL), prolymphocyte leukemia (PLL), multiple mylenoma, hairy cell leukemia (HLL) and Waldenstrom's inacroglobulinemia (WM). Additional forms of malignant lymphomas include, but are not limited to non-Hodgkin lymphoma and variants thereof, peripheral T cell lymphomas, adult T cell leukemia/lymphoma (ATL), cutaneous T-cell lymphoma (CTCL), large granular lymphocytic leukemia (LGF), Hodgkin's disease and Reed-Stcrnberg disease. Examples of cellular proliferative and/or differentiative disorders of the breast include, but are not limited to, proliferative breast disease including, e.g., epithelial hyperplasia, sclerosing adenosis, and small duct papillomas; tumors, e.g., stromal tumors such as fibroadenoma, phyllodes tumor, and sarcomas, and epithelial tumors such as large duct papilloma; carcinoma of the breast including in situ (noninvasive) carcinoma that includes ductal carcinoma in situ (including Paget 's disease) and lobular carcinoma in situ, and invasive (infiltrating) carcinoma including, but not limited to, invasive ductal carcinoma, invasive lobular carcinoma, medullary carcinoma, colloid (mucinous) carcinoma, tubular carcinoma, and invasive papillary carcinoma, and miscellaneous malignant neoplasms. Disorders in the male breast include, but are not limited to, gynecomastia and carcinoma.

Pharmaceutical Compositions and Routes of Administration

As used herein, the compounds of this invention, including the compounds of formulae described herein, are defined to include pharmaceutically acceptable derivatives or prodrugs thereof. A "pharmaceutically acceptable derivative or prodrug" means any pharmaceutically acceptable salt, ester, salt of an ester, or other derivative of a compound of this invention which, upon administration to a recipient, is capable of providing (directly or indirectly) a compound of this invention. Particularly favored derivatives and prodrugs arc those that increase the bioavailability of the compounds of this invention when such compounds arc administered to a mammal (e.g., by allowing an orally administered compound to be more readily absorbed into the blood) or which enhance delivery of the parent compound to a biological compartment (e.g., the brain or lymphatic system) relative to the parent species. Preferred prodrugs include derivatives where a group which enhances aqueous solubility or active transport through the gut membrane is appended to the structure of formulae described herein. The compounds of this invention may be modified by appending appropriate functionalities to enhance selective biological properties. Such modifications are known in the art and include those which increase biological penetration into a given biological compartment (e.g., blood, lymphatic system, central nervous system), increase oral availability, increase solubility to allow administration by injection, alter metabolism and alter rate of excretion.

Pharmaceutically acceptable salts of the compounds of this invention include those derived from pharmaceutically acceptable inorganic and organic acids and bases. Examples of suitable acid salts include acetate, adipate, bcnzoate, benzenesulfonate, butyrate, citrate, digluconate, dodecylsulfate, formate, fumarate, glycolate, hemisulfate, heptanoate, hexanoate, hydrochloride, hydrobromide, hydroiodidc, lactate, maleate, malonate, methanesulfonatc, 2-naphthalencsulfonate, nicotinate, nitrate, palmoate, phosphate, picrate, pivalate, propionate, salicylate, succinate, sulfate, tartrate, tosylate and undecanoate. Salts derived from appropriate bases include alkali metal (e.g., sodium), alkaline earth metal (e.g., magnesium), ammonium and N-(alkyl)₄ salts. This invention also envisions the quaternization of any basic nitrogen-containing groups of the compounds disclosed herein. Water or oil-soluble or dispcrsible products may be obtained by such quatcrnization.

The compounds of the formulae described herein can, for example, be administered by injection, intravenously, intraarterially, subdermally, intraperitoncally, intramuscularly, or subcutaneously; or orally, buccally, nasally, transmucosally, topically, in an ophthalmic preparation, or by inhalation, with a dosage ranging from about 0.001 to about 100 mg/kg of body weight, or according to the requirements of the particular drug. The methods herein contemplate administration of an effective amount of compound or compound composition to achieve the desired or stated effect. Typically, the pharmaceutical compositions of this invention will be administered from about 1 to about 6 times per day or alternatively, as a continuous infusion. Such administration can be used as a chronic or acute therapy. The amount of active ingredient that may be combined with the carrier materials to produce a single dosage form will vary depending upon the host treated and the particular mode of administration. A typical preparation will contain from about 5% to about 95% active compound (w/w). Alternatively, such preparations contain from about 20% to about 80% active compound.

Lower or higher doses than those recited above may be required. Specific dosage and treatment regimens for any particular patient will depend upon a variety of factors, including the activity of the specific compound employed, the age, body weight, general health status, sex, diet, time of administration, rate of excretion, drug combination, the severity and course of the disease, condition or symptoms, the patient's disposition to the disease, condition or symptoms, and the judgment of the treating physician.

Upon improvement of a patient's condition, a maintenance dose of a compound, composition or combination of this invention may be administered, if necessary. Subsequently, the dosage or frequency of administration, or both, may be reduced, as a function of the symptoms, to a level at which the improved condition is retained. Patients may, however, require intermittent treatment on a long-term basis upon any recurrence of disease symptoms.

Pharmaceutical compositions of this invention comprise a compound of the formulae described herein or a pharmaceutically acceptable salt thereof; an additional agent including for example, morphine or codeine; and any pharmaceutically acceptable carrier, adjuvant or vehicle. Alternate compositions of this invention comprise a compound of the formulae described herein or a pharmaceutically acceptable salt thereof; and a pharmaceutically acceptable carrier, adjuvant or vehicle. The compositions delineated herein include the compounds of the formulae delineated herein, as well as additional therapeutic agents if present, in amounts effective for achieving a modulation of disease or disease symptoms.

The term "pharmaceutically acceptable carrier or adjuvant" refers to a carrier or adjuvant that may be administered to a patient, together with a compound of this invention, and which does not destroy the pharmacological activity thereof and is nontoxic when administered in doses sufficient to deliver a therapeutic amount of the compound.

Pharmaceutically acceptable carriers, adjuvants and vehicles that may be used in the pharmaceutical compositions of this invention include, but arc not limited to, ion exchangers, alumina, aluminum stcarate, lecithin, self-emulsifying drug delivery systems (SEDDS) such as d-α-tocopherol polyethylencglycol 1000 succinate, surfactants used in pharmaceutical dosage forms such as Tweens or other similar polymeric delivery matrices, scrum proteins, such as human serum albumin, buffer substances such as phosphates, glycine, sorbic acid, potassium sorbatc, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes, such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidonc, cellulose-based substances, polyethylene glycol, sodium carboxymcthylccllulose, polyacrylatcs, waxes, polyethylene-polyoxypropylene- block polymers, polyethylene glycol and wool fat. Cyclodextrins such as α-, β-, and γ-cyclodcxtrin, may also be advantageously used to enhance delivery of compounds of the formulae described herein. Tlic pharmaceutical compositions of this invention may be administered orally, parcntcrally, by inhalation spray, topically, rectally, nasally, buccally, vaginally or via an implanted reservoir, preferably by oral administration or administration by injection. The pharmaceutical compositions of this invention may contain any conventional non-toxic pharmaceutically-acceptable carriers, adjuvants or vehicles. In some cases, the pH of the formulation may be adjusted with pharmaceutically acceptable acids, bases or buffers to enhance the stability of the formulated compound or its delivery form. The term parenteral as used herein includes subcutaneous, intracutaneous, intravenous, intramuscular, intraarticular, intraarterial, intrasynovial, intrastcrnal, intrathecal, intralesional and intracranial injection or infusion techniques.

The pharmaceutical compositions may be in the form of a sterile injectable preparation, for example, as a sterile injectable aqueous or oleaginous suspension. This suspension may be formulated according to techniques known in the art using suitable dispersing or wetting agents (such as, for example, Twecn 80) and suspending agents. The sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parentcrally acceptable diluent or solvent, for example, as a solution in 1,3-butancdiol. Among the acceptable vehicles and solvents that may be employed are mannitol, water, Ringer's solution and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose, any bland fixed oil may be employed including synthetic mono- or diglycerides. Fatty acids, such as oleic acid and its glyccridc derivatives are useful in the preparation of injectables, as are natural pharmaceutically-acceptable oils, such as olive oil or castor oil, especially in their polyoxycthylated versions. These oil solutions or suspensions may also contain a long-chain alcohol diluent or dispersant, or carboxymethyl cellulose or similar dispersing agents which arc commonly used in the formulation of pharmaceutically acceptable dosage forms such as emulsions and or suspensions. Other commonly used surfactants such as Tweens or Spans and/or other similar emulsifying agents or bioavailability enhancers which are commonly used in the manufacture of pharmaceutically acceptable solid, liquid, or other dosage foπns may also be used for the purposes of formulation. The pharmaceutical compositions of this invention may be orally administered in any orally acceptable dosage form including, but not limited to, capsules, tablets, emulsions and aqueous suspensions, dispersions and solutions. In the case of tablets for oral use, carriers which are commonly used include lactose and corn starch. Lubricating agents, such as magnesium stearate, are also typically added. For oral administration in a capsule form, useful diluents include lactose and dried com starch. When aqueous suspensions and/or emulsions are administered orally, the active ingredient may be suspended or dissolved in an oily phase is combined with emulsifying and/or suspending agents. Jf desired, certain sweetening and/or flavoring and/or coloring agents may be added.

The pharmaceutical compositions of this invention may also be administered in the form of suppositories for rectal administration. These compositions can be prepared by mixing a compound of this invention with a suitable non-irritating excipient which is solid at room temperature but liquid at the rectal temperature and therefore will melt in the rectum to release the active components. Such materials include, but are not limited to, cocoa butter, beeswax and polyethylene glycols.

ITic pharmaceutical compositions of this invention may be administered by nasal aerosol or inhalation. Such compositions are prepared according to techniques well-known in the art of pharmaceutical formulation and may be prepared as solutions in saline, employing benzyl alcohol or other suitable preservatives, absorption promoters to enhance bioavailability, fluorocarbons, and/or other solubilizing or dispersing agents known in the art.

When the compositions of this invention comprise a combination of a compound of the formulae described herein and one or more additional therapeutic or prophylactic agents, both the compound and the additional agent should be present at dosage levels of between about 1 to 100%, and more preferably between about 5 to 95% of the dosage normally administered in a monotherapy regimen. The additional agents may be administered separately, as part of a multiple dose regimen, from the compounds of this invention. Alternatively, those agents may be part of a single dosage form, mixed together with the compounds of this invention in a single composition. Screening Assays

The invention provides methods (also referred to herein as "screening assays") for identifying polypeptides which modulate the activity of one or more Notch complexes. The binding affinity of polypeptides to Notch can measured using the methods described herein, for example, by using a titration binding assay. Notch complex lacking MAML (i.e., a complex of ICN and CSL) be exposed to varying concentrations of a candidate compound (i.e., polypeptide) (e.g., 1 nM, 10 nM, 100 nM, 1 μM, 10 μM, 100 μM, 1 mM, and 10 mM) and binding can be measured using surface plasmon resonance to determine the Kd for binding. Candidate compounds could also be screened for biological activity in vivo, for example, by measuring expression of a Notch responsive reporter in a suitable cell, e.g., in MOLT-4 cells. Cell permeability screening assays in which fluorescently labeled candidate compounds arc applied to intact cells, which arc then assayed for cellular fluorescence by microscopy or high-throughput cellular fluorescence detection can also be used.

The assays described herein can be performed with individual candidate compounds or can be performed with a plurality of candidate compounds. Where the assays are performed with a plurality of candidate compounds, the assays can be performed using mixtures of candidate compounds or can be run in parallel reactions with each reaction having a single candidate compound. The test compounds or agents can be obtained using any of the numerous approaches in combinatorial library methods known in the art.

Other applications

A number of embodiments of the invention have been described. Nevertheless, it will be understood that various modifications may be made without departing from the spirit and scope of the invention. Accordingly, other embodiments are within the scope of the following claims.

Claims

1. A modified polypeptide of Formula (1),

Formula (I) Wherein: each Ri and R₂ are independently H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, hcteroarylalkyl, or heterocyclylalkyl; each R3 is independently alkyl, alkenyl, alkynyl; [R₄-K.-R₄],,; each of which is substituted with 0-6 R₅; each R₄ is independently alkyl, alkenyl, or alkynyl; each R₅ is independently is halo, alkyl, OR₆, N(R₆K SR₆, SOR₆, SO₂R₆, CO₂R₆, R₆, a fluorescent moiety, or a radioisotope;

each K is independently O, S, SO, SO₂, CO, CO₂, CONR₆, or X ^ each R₆ is independently H, alkyl, or a therapeutic agent; n is an integer from 1-4; x is 3, 4 or 6; y and w are independently integers from 0-100; z is an integer from 1-10; and each Xaa is independently an amino acid; wherein the modified polypeptide comprises at least 8 contiguous amino acids of a MAML polypeptide except that: (a) within the 8 contiguous amino acids the side chains of at least one pair of amino acids separated by 3, 4 or 6 amino acids is replaced by the linking group R3 which connects the alpha carbons of the pair of amino acids as depicted in Formula 1 and (b) the alpha carbon of the first of the pair of amino acids is substituted with Rj as depicted in formula I and the alpha carbon of the second of the pair of amino acids is substituted with R₂ as depicted in Formula I and wherein and N or C can be substituted by PEG, spermine, or a carbohydrate.

2. The modified polypeptide of claim 1 , wherein the MAML polypeptide comprises any of SEQ ID NOs: 1 to 7.

3. The polypeptide of claim 1, wherein the modified polypeptide binds a complex comprising CSL and ICN.

4. The modified polypeptide of claim 1, wherein the MAML polypeptide ins selected from human MAML-I, MAML-2 and MAML-3.

5. The polypeptide of claim 1, wherein the polypeptide reduces the viability of at least one of M0LT4 cells, ALL-SIL T-ALL cells, KOPTKl T-ALL cells and TALLl cells.

6. The modified polypeptide of claim 1 , wherein x is 3.

7. The modified polypeptide of claim 1 , wherein x is 4.

8. The modified polypeptide of claim 1, wherein x is 6.

9. The modified polypeptide of claim 1 , wherein x is 2 or 6; Rj is an alkenyl containing a single double bond, and both Ri and R₂ are H.

10. The modified polypeptide of claim 1 , wherein each y is independently an integer between 3 and 15.

11. The modified polypeptide of claim 1 , wherein R| and R₂ are each independently H or Ci-Cή alkyl.

12. The modified polypeptide of claim 1, wherein Ri and R₂ are each independently C₁-C₃ alkyl.

13. The modified polypeptide of claim 11, wherein at least one of Ri and R₂ are methyl.

14. The modified polypeptide of claim 12, wherein Ri and Ri are methyl.

15. The modified polypeptide of claim 1 , wherein R₃ is alkyl.

16. The modified polypeptide of claim 14, wherein x is 3.

17. The modified polypeptide of claim 15, wherein R₃ is C« alkyl.

18. The modified polypeptide of claim 14, wherein x is 6.

19. The modified polypeptide of claim 17, wherein R₃ is C| 1 alkyl.

20. The modified polypeptide of claim 1, wherein R;, is alkenyl.

21. The modified polypeptide of claim 18, wherein x is 3.

22. The modified polypeptide of claim 20, wherein R3 is Cg alkenyl.

23. The modified polypeptide of claim 19, wherein x is 6.

24. The modified polypeptide of claim 19, wherein R₃ is Cn alkenyl.

25. The modified polypeptide of claim 1 , wherein R₃ is a straight chain alkyl, alkenyl, or alkynyl.

26. ^'Die modified polypeptide of claim 1, wherein R₃ is [R₄-K.-R4]; and R₄ is a straight chain alkyl, alkenyl, or alkynyl.

27. The modified polypeptide of claim 1 , wherein the polypeptide comprises at least 8 contiguous amino acids of SEQ ID NO:2, SEQ ID NO:3 or SEQ ID NO:4 except that within the 8 contiguous amino the side chains of at least one pair of amino acids separated by 3 or 6 amino acids is replaced the linking group R3 as depicted in Formula I which connects the alpha carbons of the pair of amino acids and the alpha carbon of the first of the pair of amino acids is substituted with R| as depicted in formula I and the alpha carbon of the second of the pair of amino acids is substituted with R₂ as depicted in Formula 1.

28. The modified polypeptide of claim 1 wherein [Xaa]_w comprises an amino acid sequence selected from: AVMERL, RLRRRl, LCR, LCRRHH, TCE, RYE,TCEARYCEARYE, LERQHT,HTF, and HTFALH.

29. The modified polypeptide of claim 15, wherein at least one of R ₁ or R₂ is alkyl.

30. The modified polypeptide of claim 1 1 , wherein each R| and R₂ is independently H or C₁-C₃ alkyl.

31. The modified polypeptide of claim 1, wherein R ₁ and R₂ arc methyl.

32. The modified polypeptide of claim 1 , wherein x is 3 or 6 and z is 1.

33. The modified polypeptide of claim 1, wherein Rj is Cg or Ci ₁ alkyl or alkenyl.

37. The modified polypeptide of claim 1 , further comprising a copolymer of lactic and glycolic acid

38. The modified polypeptide of claim 1 , further comprising a PEG.

39. The modified polypeptide of claim 1 , further comprising an targeting moiety. 40. The modified polypeptide of claim 1 , further comprising a biotin moiety.

41. A method of making a polypeptide of Formula (III), comprising providing a polypeptide of Foπnula (II); and

Formula (II) treating the compound of Formula (II) with a catalyst to promote a ring closing metathesis, thereby providing a compound of Formula (III)

Formula (III) wherein each R| and Ro are independently H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl; heteroarylalkyl; or heterocyclylalkyl; each n is independently an integer from 1-15; x is 3, 4, or 6 each y is independently an integer from 0-100; z is an integer from 1-3; and each Xaa is independently an amino acid; and wherein the polypeptide comprises an alpha helical structure in aqueous solution.

42. The method of claim 41 , wherein the polypeptide binds to a complex comprising ICN and CSL.

43. The method of claim 41 , wherein the catalyst is a ruthenium catalyst.

44. The method of claim 41 , further comprising providing a reducing agent or oxidizing agent subsequent to the ring closing metathesis.

45. The method of claim 44, wherein the reducing agent is H₂ or oxidizing agent is osmium tetroxide

46. A method of treating a subject comprising administering to the subject a compound of claim 1.

47. The method of claim 46, further comprising administering an additional therapeutic agent.

48. A method of treating cancer in a subject comprising administering to the subject a compound of claim 1.

49. The method of claim 48, further comprising administering an additional therapeutic agent.

50. A library of compounds of claim 1, formula (I).

51. A compound having the formula

R, is -CH₂CH₂COOH [E] or -CH₂COOH [D] or R, and R₈ together are R_x;

R₂ is -CH₂CH(CH₃):. [L] Or -CH₂CH₂CH₂N(H)C(NH)NH₂ [R];

R₃ Is -CH₂CH₂COOH [E]

R₄ is -CH₂CH₂CH₂N(H)C(NH)NH₂ [R];

R₅ IS -CH₂CH₂C(O)NH₂ [Q], -CH₂CH₂COOH [E], or CH₂CH₂CH₂N(H)C(NH)NH₂ [R]; or R₅ and R₉ together are Ry; or R₅ and R₁₂ together arc Rx;

ΛΛΛΛ CH₂

R₆ is -CH₂OH [S], M ™H" ₁ [H] or -CH₂COOH [D];

R₇ IS -C(OH)CH₃ [T];

R₈ is benzyl [FJ, -CH₂CH(CHj)₂ [L], -CH(CH₃)₂ [V] or R₁ and Rg together are R_x;

R₉ is selected from: -CH₃ [A] or -CH₂CH₂C(O)NH₂ [Q] and -CH₂OH [S]; or R₅ and R₉ together are R_y;

R₁O iS -CH₂CH(CHs)₂ [L]; R, i is

R_n is -CH₂CH₂C(O)NH₂ [Q] and -CH₂OH [S]; or R₅ and R₁₂ together arc Rx provided that when Ri and Rg together are Rx, R5 and R₉ are not together Ry and R₅ and Ri₂ arc not together R_x; further provided that when R₅ and R9 together are Ry, R| and Rs are not together R_x and R₅ and R_!2 are not together R_x; further provided that when R₅ and Rj₂ arc together R_x, R₅ and R<; are not together R_y and Ri and Rg are not together R_x;

R_x and R_y alkyl, alkenyl, alkynyl; [R_xI-K-R_x)],,; each of which is substituted with 0-6 R_x2;

R_xI is alkyl, alkenyl, or alkynyl;

R_x2 is halo, alkyl, OR_x3, N(R_x3)₂, SR_x3, SOR_x3, SO₂Rx₃, CO₂R_x3, R_x3, a fluorescent moiety, or a radioisotope;

K is O, S, SO, SO₂, CO, CO₂, C0NR_x3, or '* ^ ; R_x3 is H, alkyl or a therapeutic agent; and

R₇. and R_w arc independently: H, hydroxyl, an amino acid, 2 to 10 amino acids linked by peptide bonds; tat; and PEG.

52. The polypeptide of claim 51 , wherein each y is independently an integer between 3 and 15.

53. The polypeptide of claim 51 , wherein R| and R₂ arc each independently H or Ci-Ce alkyl.

54 The polypeptide of claim 51 , wherein R| and R₂ arc each independently CpC₃ alkyl.

55. The polypeptide of claim 51, wherein at least one of Rj and R₂ are methyl.

56. The polypeptide of claim 51 , wherein Ri and R₂ are methyl.

57. The polypeptide of claim 51 , wherein R₃ is alkyl.

58. The polypeptide of claim 51, wherein x is 3.

59. The polypeptide of claim 51, wherein R₃ is Cs alkyl.

60. The polypeptide of claim 51 , wherein x is 6.

61. The polypeptide of claim 51, wherein R₃ is Ci ₁ alkyl.

62. The polypeptide of claim 51 , wherein Rj is alkenyl.

63. The polypeptide of claim 51 , wherein R₃ is Cg alkenyl.

64. The polypeptide of claim 51, wherein R₃ is Cn alkenyl.

65. The polypeptide of claim 51, wherein R₃ is a straight chain alkyl, alkenyl, or alkynyl.

66. The polypeptide of claim 51 , wherein R₃ is [R₄-K-R₄]; and R₄ is a straight chain alkyl, alkenyl, or alkynyl.

66. The polypeptide of claim 51 , wherein x is 3 and z is 1.

67. ITic polypeptide of claim 51 , wherein the polypeptide is transported through the cell membrane.

68. The polypeptide of claim 1 wherein polypeptide comprises an amino acid sequence selected from SEQ ID NOs:8, 9 and 10 wherein: (a) the side chains of amino acids 8 and 12 are replaced by the linking group R₃ which connects the alpha carbons of amino acids 8 and 12 as depicted in formula I; and (b) the alpha carbon of amino acid 8 is substituted with Ri as depicted in formula I and the alpha carbon of amino acid 12 is substituted with R_∑as depicted in formula I.