Classifications

• • C—CHEMISTRY; METALLURGY
  • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
  • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
  • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
  • C12Q1/48—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving transferase
  • C12Q1/485—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving transferase involving kinase
• • G—PHYSICS
  • G01—MEASURING; TESTING
  • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
  • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
  • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
  • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
  • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
  • G01N33/573—Immunoassay; Biospecific binding assay; Materials therefor for enzymes or isoenzymes

Definitions

• the present invention relates to kinase sensors comprising a metal chelator, an amino acid and a fluorophore, where the chelator comprises a quinoline group and where the fluorophore and amino acid are both conjugated to the quinoline.
• the invention also relates to methods of using these kinase sensors as well as kits comprising the kinase sensors.
• Protein kinases are a class of important enzymes that catalyze the transfer of a phosphate group from ATP to serine, threonine, tyrosine, and histidine residues of peptides and proteins.
• the specificity of kinases is controlled by kinase recognition motifs, which are amino acid residues surrounding the amino acid to be phosphorylated. This phosphorylation reaction is ubiquitous in life and is an essential step in many intracellular signal transduction pathways.
• the importance of protein phosphorylation as a regulatory process means that kinase inhibitors are potentially highly valuable therapeutic agents for many diseases.
• Sensitive and broadly applicable methods for real time measurement of kinase activity are acutely needed by the biosciences research community, from basic investigation of enzyme mechanisms to systems biology to drug discovery.
• Traditional assays utilize radioactive material ⁇ e.g., P), which can be expensive, dangerous and can pose problems for disposal.
• Other methods for studying kinases include fluorescence.
• current fluorometric methods while safer than radioactivity, may not be bright enough to discern signal-to-noise ratio.
• background fluorescence in the assay environment may also interfere with accurate fluorescent measurement.
• the present invention relates to improved kinase sensors.
• One embodiment of the present invention provides a kinase sensor comprising a metal chelator, one or more amino acids and a fluorophore, wherein the chelator comprises a quinoline group and both the fluorophore and amino acid are conjugated to the quinoline group.
• the one or more amino acids comprise a kinase substrate.
• the quinoline group is substituted with a hydroxy group, an amino group, an amide group, a sulfonamide group or a thiol group.
• the quinoline group chelates magnesium.
• the fluorophore is selected from the group consisting of dansyl, xanthene, cyanine, borapolyazaindacene, pyrene, naphthalene, coumarin, oxazine, and derivatives thereof. More particularly, the fluorophore is a coumarin, a xanthene or a derivative thereof.
• the kinase substrate is a peptide. More particularly, the peptide comprises a kinase recognition site and at least one amino acid residue selected from serine, threonine, or tyrosine that is subject to phosphorylation by the kinase.
• Another embodiment of the invention provides a kinase sensor having the formula
• R is H, alkyl, substituted alkyl, alkoxy, substituted alkoxy, acyl, acylamino, acyloxy, amino, substituted amino, aminocarbonyl, aminothiocarbonyl, aminocarbonylamino, aminothiocarbonylamino, aminocarbonyloxy, aminosulfonyl, aminosulfonyloxy, aminosulfonylamino, amidino, carboxyl, carboxyl ester, (carboxyl ester)amino, (carboxyl ester)oxy, cyano, halo, hydroxy, nitro, SO3H, sulfonyl, substituted sulfonyl, sulfonyloxy, thioacyl, thiol, alkylthio, substituted alkylthio, aryl, substituted aryl, heteroaryl, substituted heteroaryl, cycloalkyl, substituted cycloalkyl, heterocycly
• R 2 is a fluorophore, H, alkyl, substituted alkyl, alkoxy, substituted alkoxy, acyl, acylamino, acyloxy, amino, substituted amino, aminocarbonyl, aminothiocarbonyl, aminocarbonylamino, aminothiocarbonylamino, aminocarbonyloxy, aminosulfonyl, aminosulfonyloxy, aminosulfonylamino, amidino, carboxyl, carboxyl ester, (carboxyl ester)amino, (carboxyl ester)oxy, cyano, halo, hydroxy, nitro, SO 3 H, sulfonyl, substituted sulfonyl, sulfonyloxy, thioacyl, thiol, alkylthio, substituted alkylthio, aryl, substituted aryl, heteroaryl, substituted heteroaryl, cycloalkyl, substituted cycloal
• R 4 is a fluorophore, H, alkyl, substituted alkyl, alkoxy, substituted alkoxy, acyl, acylamino, acyloxy, amino, substituted amino, aminocarbonyl, aminothiocarbonyl, aminocarbonylamino, aminothiocarbonylamino, aminocarbonyloxy, aminosulfonyl, aminosulfonyloxy, aminosulfonylamino, amidino, carboxyl, carboxyl ester, (carboxyl ester)amino, (carboxyl ester)oxy, cyano, halo, hydroxy, nitro, SO 3 H, sulfonyl, substituted sulfonyl, sulfonyloxy, thioacyl, thiol, alkylthio, substituted alkylthio, aryl, substituted aryl, heteroaryl, substituted heteroaryl, cycloalkyl, substituted cycloal
• R 5 is a fluorophore, H, alkyl, substituted alkyl, alkoxy, substituted alkoxy, acyl, acylamino, acyloxy, amino, substituted amino, aminocarbonyl, aminothiocarbonyl, aminocarbonylamino, aminothiocarbonylamino, aminocarbonyloxy, aminosulfonyl, aminosulfonyloxy, aminosulfonylamino, amidino, carboxyl, carboxyl ester, (carboxyl ester)amino, (carboxyl ester)oxy, cyano, halo, hydroxy, nitro, SO 3 H, sulfonyl, substituted sulfonyl, sulfonyloxy, thioacyl, thiol, alkylthio, substituted alkylthio, aryl, substituted aryl, heteroaryl, substituted heteroaryl, cycloalkyl, substituted cycloal
• R 6 is a fluorophore, H, alkyl, substituted alkyl, alkoxy, substituted alkoxy, acyl, acylamino, acyloxy, amino, substituted amino, aminocarbonyl, aminothiocarbonyl, aminocarbonylamino, aminothiocarbonylamino, aminocarbonyloxy, aminosulfonyl, aminosulfonyloxy, aminosulfonylamino, amidino, carboxyl, carboxyl ester, (carboxyl ester)amino, (carboxyl ester)oxy, cyano, halo, hydroxy, nitro, SO 3 H, sulfonyl, substituted sulfonyl, sulfonyloxy, thioacyl, thiol, alkylthio, substituted alkylthio, aryl, substituted aryl, heteroaryl, substituted heteroaryl, cycloalkyl, substituted cycloal
• R 2 , R 3 , R 4 , R 5 and R 6 is a fluorophore
• R 7 is H, alkyl, substituted alkyl, carbonyl, peptide, or a protecting group
• R 8 is H, alkyl, substituted alkyl, carbonyl, peptide or a protecting group
• L is a linker; and Y is a peptide or H;
• n 1-5; or a tautomer, stereoisomer, or salt thereof.
• R is a fluorophore.
• the fluorophore is dansyl, xanthene, cyanine, borapolyazaindacene, pyrene, naphthalene, coumarin, oxazine, or derivatives thereof.
• the fluorophore is a coumarin, a xanthene or a derivative thereof.
• the fluorophore is:
• R 9 and R 10 are each independently a halogen, -SO 3 H, substituted sulfonyl, or H.
• L is a covalent bond
• Y is H.
• R is hydroxy.
• R 2 , R 3 , R 5 and R 6 are all H.
• R 7 is H or FMOC.
• R 8 is H.
• Y is a peptide. More particularly, the peptide comprises a kinase recognition site and at least one amino acid residue selected from serine, threonine, or tyrosine that is subject to phosphorylation by a kinase.
• the position indicated with a TM ⁇ bond is in the S configuration.
• Another embodiment of the invention provides salt of the kinase sensor, wherein the salt is magnesium.
• Another embodiment of the invention provides a kinase sensor having the formula
• R 7 is H, a peptide or a protecting group
• R 9 is a halogen, -SO 3 H, substituted sulfonyl, or H;
• R 10 is a halogen, -SO 3 H, substituted sulfonyl, or H;
• L is a linker
• Y is a peptide or H
• n 1-5; or a tautomer, stereoisomer, or salt thereof.
• L is a covalent bond
• Y is H.
• R 9 and R 10 are both fluorine.
• R 7 is H.
• Another embodiment of the present invention provides a method of detecting kinase activity comprising
• the measured fluorescence is selected from the group consisting of intensity, excitation or emission wavelength, distribution of fluorescence, fluorescence lifetime, fluorescence polarization, or a combination thereof.
• Another embodiment of the present invention provides a method of detecting kinase activity, wherein the method comprises:
• kits comprising:
• a kinase sensor comprising a metal chelator, one or more amino acids and a fluorophore, wherein the chelator comprises a quinoline group and both the fluorophore and amino acid are conjugated to the quinoline group and, and wherein the amino acids comprise a kinase recognition site and a phosphorylation site.
• the current invention involves strategic attachment of long wavelength, highly absorptive fluorophores to kinase substrate peptides such that phosphorylation of the substrate peptides results in a fluorescence change and/or increase.
• This fluorescence change and/or increase is mediated by metal ion binding to both the fluorophore moiety and the newly introduced phosphate moiety.
• the current invention also provides modularity so that a large variety of kinase substrate peptides can be readily prepared by standard solid phase peptide synthesis methods.
• the present invention therefore provides kinase sensors comprising a metal chelator, one or more an amino acids and a fluorophore, wherein the chelator comprises a quinoline group and wherein the fluorophore and amino acid are both conjugated to the quinoline. Furthermore, kinase subrates can be conjugated to the quinoline group through the amino acid moiety.
• Alkyl refers to monovalent saturated aliphatic hydrocarbyl groups having from 1 to 10 carbon atoms and preferably 1 to 6 carbon atoms. This term includes, by way of example, linear and branched hydrocarbyl groups such as methyl (CH3-), ethyl (CH3CH2-), ⁇ -propyl (CH 3 CH 2 CH 2 -), isopropyl ((CH 3 ) 2 CH-), n-butyl (CH 3 CH 2 CH 2 CH 2 -), isobutyl ((CH 3 ) 2 CHCH 2 -), sec-butyl ((CH 3 )(CH 3 CH 2 )CH-), f-butyl ((CH 3 ) 3 C-), n-pentyl (CH 3 CH 2 CH 2 CH 2 CH 2 -), and neopentyl ((CH 3 ) 3 CCH 2 -).
• Substituted alkyl refers to an alkyl group having from 1 to 5, preferably 1 to 3, or more preferably 1 to 2 substituents selected from the group consisting of alkoxy, substituted alkoxy, acyl, acylamino, acyloxy, amino, substituted amino, aminocarbonyl, aminothiocarbonyl, aminocarbonylamino, aminothiocarbonylamino, aminocarbonyloxy, aminosulfonyl, aminosulfonyloxy, aminosulfonylamino, amidino, aryl, substituted aryl, aryloxy, substituted aryloxy, arylthio, substituted arylthio, carboxyl, carboxyl ester, (carboxyl ester)amino, (carboxyl ester)oxy, cyano, cycloalkyl, substituted cycloalkyl, cycloalkyloxy, substituted cycloalkyloxy, cycloalkyloxy,
• Alkoxy refers to the group -O-alkyl wherein alkyl is defined herein. Alkoxy includes, by way of example, methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, t-butoxy, sec-butoxy, and n-pentoxy.
• Substituted alkoxy refers to the group -O-(substituted alkyl) wherein substituted alkyl is defined herein.
• Acyl refers to the groups H-C(O)-, alkyl-C(O)-, substituted alkyl-C(O)-, alkenyl-C(O)-, substituted alkenyl-C(O)-, alkynyl-C(O)-, substituted alkynyl-C(O)-, cycloalkyl-C(O)-, substituted cycloalkyl-C(O)-, cycloalkenyl-C(O)-, substituted cycloalkenyl-C(O)-, aryl-C(O)-, substituted aryl-C(O)-, heteroaryl-C(O)-, substituted heteroaryl-C(O)-, heterocyclic-C(O)-, and substituted heterocyclic-C(O)-, wherein alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, substituted
• Acylamino refers to the groups -NRC(O)alkyl, -NRC(O)substituted alkyl, -NRC(O)cycloalkyl, -NRC(O)substituted cycloalkyl, -NRC(O)cycloalkenyl, -NRC(O)substituted cycloalkenyl, -NRC(O)alkenyl, -NRC(O)substituted alkenyl, -NRC(O)alkynyl, - NRC(O)substituted alkynyl, -NRC(O)aryl, -NRC(O)substituted aryl, -NRC(O)heteroaryl, -NRC(O)substituted heteroaryl, -NRC(O)heterocyclic, and -NRC(O)substituted heterocyclic where
• Acyloxy refers to the groups alkyl-C(O)O-, substituted alkyl-C(O)O-, alkenyl-C(O)O-, substituted alkenyl-C(O)O-, alkynyl-C(O)O-, substituted alkynyl-C(O)O-, aryl-C(O)O-, substituted aryl-C(O)O-, cycloalkyl-C(O)O-, substituted cycloalkyl-C(O)O-, cycloalkenyl-C(O)O-, substituted cycloalkenyl-C(O)O-, heteroaryl-C(O)O-, substituted heteroaryl-C(O)O-, heterocyclic-C(O)O-, and substituted heterocyclic-C(O)O- wherein alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkyn
• Amino refers to the group -NH 2 .
• Substituted amino refers to the group -NR'R" where R' and R" are independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycloalkenyl, heteroaryl, substituted heteroaryl, heterocyclic, substituted heterocyclic, -SCValkyl, -SCVsubstituted alkyl, -SCValkenyl, -SCVsubstituted alkenyl, -SCVcycloalkyl, -SCVsubstituted cylcoalkyl, -SCVcycloalkenyl, -SC> 2 -substituted cylcoalkenyl,-SO 2 -aryl, -SCV
• R' is hydrogen and R" is alkyl
• the substituted amino group is sometimes referred to herein as alkylamino.
• R' and R" are alkyl
• the substituted amino group is sometimes referred to herein as dialkylamino.
• a monosubstituted amino it is meant that either R' or R" is hydrogen but not both.
• a disubstituted amino it is meant that neither R' nor R" are hydrogen.
• Aminocarbonyl refers to the group -C(O)N R 10 R 11 where R 10 and R 11 are independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycloalkenyl, heteroaryl, substituted heteroaryl, heterocyclic, and substituted heterocyclic and where R 10 and R 11 are optionally joined together with the nitrogen bound thereto to form a heterocyclic or substituted heterocyclic group, and wherein alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycloalkenyl, aryl,
• Aminothiocarbonyl refers to the group -C(S)NR 10 R 11 where R 10 and R 11 are independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycloalkenyl, heteroaryl, substituted heteroaryl, heterocyclic, and substituted heterocyclic and where R 10 and R 11 are optionally joined together with the nitrogen bound thereto to form a heterocyclic or substituted heterocyclic group, and wherein alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycloalkenyl, aryl
• Aminocarbonylamino refers to the group -NRC(O)NR 10 R 11 where R is hydrogen or alkyl and R 10 and R 11 are independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycloalkenyl, heteroaryl, substituted heteroaryl, heterocyclic, and substituted heterocyclic and where R 10 and R 11 are optionally joined together with the nitrogen bound thereto to form a heterocyclic or substituted heterocyclic group, and wherein alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycl
• Aminothiocarbonylammo refers to the group -NRC(S)NR 10 R 11 where R is hydrogen or alkyl and R and R are independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycloalkenyl, heteroaryl, substituted heteroaryl, heterocyclic, and substituted heterocyclic and where R 10 and R 11 are optionally joined together with the nitrogen bound thereto to form a heterocyclic or substituted heterocyclic group, and wherein alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycl
• Aminocarbonyloxy refers to the group -0-C(O)NR 10 R 11 where R 10 and R 11 are independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycloalkenyl, heteroaryl, substituted heteroaryl, heterocyclic, and substituted heterocyclic and where R 10 and R 11 are optionally joined together with the nitrogen bound thereto to form a heterocyclic or substituted heterocyclic group, and wherein alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycloalkenyl, aryl
• Aminosulfonyl refers to the group -SO 2 NR 10 R 11 where R 10 and R 11 are independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycloalkenyl, heteroaryl, substituted heteroaryl, heterocyclic, and substituted heterocyclic and where R and R are optionally joined together with the nitrogen bound thereto to form a heterocyclic or substituted heterocyclic group, and wherein alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycloalkenyl, aryl, substituted
• Aminosulfonyloxy refers to the group -0-SO 2 NR 10 R 11 where R 10 and R 11 are independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycloalkenyl, heteroaryl, substituted heteroaryl, heterocyclic, and substituted heterocyclic and where R 10 and R 11 are optionally joined together with the nitrogen bound thereto to form a heterocyclic or substituted heterocyclic group, and wherein alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycloalkenyl, substituted cycloal
• Aminosulfonylamino refers to the group -NR-SO 2 NR 10 R 11 where R is hydrogen or alkyl and R 10 and R 11 are independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycloalkyenyl, heteroaryl, substituted heteroaryl, heterocyclic, and substituted heterocyclic and where R and R are optionally joined together with the nitrogen bound thereto to form a heterocyclic or substituted heterocyclic group, and wherein alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted
• Aryl refers to a monovalent aromatic carbocyclic group of from 6 to 14 carbon atoms having a single ring (e.g., phenyl) or multiple condensed rings (e.g., naphthyl or anthryl) which condensed rings may or may not be aromatic (e.g., 2-benzoxazolinone, 2H- 1,4- benzoxazin-3(4H)-one-7-yl, and the like) provided that the point of attachment is at an aromatic carbon atom.
• Preferred aryl groups include phenyl and naphthyl.
• Substituted aryl refers to aryl groups which are substituted with 1 to 5, preferably 1 to 3, or more preferably 1 to 2 substituents selected from the group consisting of alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, alkoxy, substituted alkoxy, acyl, acylamino, acyloxy, amino, substituted amino, aminocarbonyl, aminothiocarbonyl, aminocarbonylamino, aminothiocarbonylamino, aminocarbonyloxy, aminosulfonyl, aminosulfonyloxy, aminosulfonylamino, amidino, aryl, substituted aryl, aryloxy, substituted aryloxy, arylthio, substituted arylthio, carboxyl, carboxyl ester, (carboxyl ester)amino, (carboxyl ester)oxy, cyano,
• Aryloxy refers to the group -O-aryl, where aryl is as defined herein, that includes, by way of example, phenoxy and naphthoxy.
• Substituted aryloxy refers to the group -O-(substituted aryl) where substituted aryl is as defined herein.
• Arylthio refers to the group -S-aryl, where aryl is as defined herein.
• Substituted arylthio refers to the group -S-(substituted aryl), where substituted aryl is as defined herein.
• Alkenyl refers to alkenyl groups having from 2 to 6 carbon atoms and preferably 2 to 4 carbon atoms and having at least 1 and preferably from 1 to 2 sites of alkenyl unsaturation. Such groups are exemplified, for example, by vinyl, allyl, and but-3-en-l-yl.
• Substituted alkenyl refers to alkenyl groups having from 1 to 3 substituents, and preferably 1 to 2 substituents, selected from the group consisting of alkoxy, substituted alkoxy, acyl, acylamino, acyloxy, amino, substituted amino, aminocarbonyl, aminothiocarbonyl, aminocarbonylamino, aminothiocarbonylamino, aminocarbonyloxy, aminosulfonyl, aminosulfonyloxy, aminosulfonylamino, amidino, aryl, substituted aryl, aryloxy, substituted aryloxy, arylthio, substituted arylthio, carboxyl, carboxyl ester, (carboxyl ester)amino, (carboxyl ester)oxy, cyano, cycloalkyl, substituted cycloalkyl, cycloalkyloxy, substituted cycloalkyloxy, cycloalkyloxy,
• Alkynyl refers to alkynyl groups having from 2 to 6 carbon atoms and preferably 2 to 3 carbon atoms and having at least 1 and preferably from 1 to 2 sites of alkynyl unsaturation.
• Substituted alkynyl refers to alkynyl groups having from 1 to 3 substituents, and preferably 1 to 2 substituents, selected from the group consisting of alkoxy, substituted alkoxy, acyl, acylamino, acyloxy, amino, substituted amino, aminocarbonyl, aminothiocarbonyl, aminocarbonylamino, aminothiocarbonylamino, aminocarbonyloxy, aminosulfonyl, aminosulfonyloxy, aminosulfonylamino, amidino, aryl, substituted aryl, aryloxy, substituted aryloxy, arylthio, substituted arylthio, carboxyl, carboxyl ester, (carboxyl ester)amino, (carboxyl ester)oxy, cyano, cycloalkyl, substituted cycloalkyl, cycloalkyloxy, substituted cycloalkyloxy, cycloalkyloxy
• Carboxyl or “carboxy” refers to -COOH or salts thereof.
• Carboxyl ester or “carboxy ester” refers to the groups -C(O)O-alkyl, -C(O)O-substituted alkyl, -C(O)O-alkenyl, -C(O)O-substituted alkenyl, -C(O)O-alkynyl, -C(O)O-substituted alkynyl, -C(O)O-aryl, -C(O)O-substituted aryl, -C(O)O-cycloalkyl, -C(O)O-substituted cycloalkyl, -C(O)O-cycloalkenyl, -C(O)O-substituted cycloalkenyl, -C(O)O-heteroaryl, -C(O)O-substituted heteroaryl, -C(O)O-
• (Carboxyl ester)amino refers to the group -NR-C(O)O-alkyl, substituted -NR-C(O)O-alkyl, -NR-C(O)O-alkenyl, -NR-C(O)O-substituted alkenyl, -NR-C(O)O-alkynyl, -NR-C(O)O-substituted alkynyl, -NR-C(O)O-aryl, -NR-C(O)O-substituted aryl, -NR-C(O)O-cycloalkyl, -NR-C(O)O-substituted cycloalkyl, -NR-C(O)O-cycloalkenyl, - NR-C(O)O-substituted cycloalkenyl, -NR-C(O)O-heteroaryl, -NR-NR-
• (Carboxyl ester)oxy refers to the group -O-C(O)O-alkyl, substituted -O-C(O)O-alkyl, -O-C(O)O-alkenyl, -O-C(O)O-substituted alkenyl, -O-C(O)O-alkynyl, -O-C(O)O-substituted alkynyl, -O-C(O)O-aryl, -O-C(O)O-substituted aryl, -O-C(O)O-cycloalkyl, -O-C(O)O-substituted cycloalkyl, -O-C(O)O-cycloalkenyl, -O-C(O)O-substituted cycloalkenyl, -O-C(O)O-heteroaryl, -O-C(O)
• Cyano refers to the group -CN.
• Cycloalkyl refers to cyclic alkyl groups of from 3 to 10 carbon atoms having single or multiple cyclic rings including fused, bridged, and spiro ring systems.
• suitable cycloalkyl groups include, for instance, adamantyl, cyclopropyl, cyclobutyl, cyclopentyl, and cyclooctyl.
• Substituted cycloalkyl and “substituted cycloalkenyl” refers to a cycloalkyl or cycloalkenyl group having from 1 to 5 or preferably 1 to 3 substituents selected from the group consisting of oxo, thione, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, alkoxy, substituted alkoxy, acyl, acylamino, acyloxy, amino, substituted amino, aminocarbonyl, aminothiocarbonyl, aminocarbonylamino, aminothiocarbonylamino, aminocarbonyloxy, aminosulfonyl, aminosulfonyloxy, aminosulfonylamino, amidino, aryl, substituted aryl, aryloxy, substituted aryloxy, arylthio, substituted arylthio, carboxyl, carboxyl, carboxy
• Cycloalkyloxy refers to -O-cycloalkyl.
• Substituted cycloalkyloxy refers to -O-(substituted cycloalkyl).
• Cycloalkylthio refers to -S-cycloalkyl.
• Substituted cycloalkylthio refers to -S-(substituted cycloalkyl).
• Cycloalkenyloxy refers to -O-cycloalkenyl.
• Substituted cycloalkenyloxy refers to -O-(substituted cycloalkenyl).
• Cycloalkenylthio refers to -S-cycloalkenyl.
• Substituted cycloalkenylthio refers to -S -(substituted cycloalkenyl).
• FMOC or “Fmoc” refers to a compound having the general formula (or derivatives thereof):
• Halo or "halogen” refers to fluoro, chloro, bromo and iodo.
• "Hydroxy” or “hydroxyl” refers to the group -OH.
• Heteroaryl refers to an aromatic group of from 1 to 10 carbon atoms and 1 to 4 heteroatoms selected from the group consisting of oxygen, nitrogen and sulfur within the ring.
• Such heteroaryl groups can have a single ring (e.g., pyridinyl or furyl) or multiple condensed rings (e.g., indolizinyl or benzothienyl) wherein the condensed rings may or may not be aromatic and/or contain a heteroatom provided that the point of attachment is through an atom of the aromatic heteroaryl group.
• the nitrogen and/or the sulfur ring atom(s) of the heteroaryl group are optionally oxidized to provide for the N-oxide (N ⁇ O), sulfinyl, or sulfonyl moieties.
• Preferred heteroaryls include pyridinyl, pyrrolyl, indolyl, thiophenyl, and furanyl.
• Substituted heteroaryl refers to heteroaryl groups that are substituted with from 1 to 5, preferably 1 to 3, or more preferably 1 to 2 substituents selected from the group consisting of the same group of substituents defined for substituted aryl.
• Heteroaryloxy refers to -O-heteroaryl.
• Substituted heteroaryloxy refers to the group -O-(substituted heteroaryl).
• Heteroarylthio refers to the group -S-heteroaryl.
• Substituted heteroarylthio refers to the group -S-(substituted heteroaryl).
• Heterocycle or “heterocyclic” or “heterocycloalkyl” or “heterocyclyl” refers to a saturated or unsaturated group having a single ring or multiple condensed rings, including fused bridged and spiro ring systems, from 1 to 10 carbon atoms and from 1 to 4 hetero atoms selected from the group consisting of nitrogen, sulfur or oxygen within the ring wherein, in fused ring systems, one or more the rings can be cycloalkyl, aryl or heteroaryl provided that the point of attachment is through the non-aromatic ring.
• the nitrogen and/or sulfur atom(s) of the heterocyclic group are optionally oxidized to provide for the N-oxide, sulfmyl, sulfonyl moieties.
• Substituted heterocyclic or “substituted heterocycloalkyl” or “substituted heterocyclyl” refers to heterocyclyl groups that are substituted with from 1 to 5 or preferably 1 to 3 of the same substituents as defined for substituted cycloalkyl.
• Heterocyclyloxy refers to the group -O-heterocycyl.
• Substituted heterocyclyloxy refers to the group -O-(substituted heterocycyl).
• Heterocyclylthio refers to the group -S-heterocycyl.
• Substituted heterocyclylthio refers to the group -S-(substituted heterocycyl).
• heterocycle and heteroaryls include, but are not limited to, azetidine, pyrrole, imidazole, pyrazole, pyridine, pyrazine, pyrimidine, pyridazine, indolizine, isoindole, indole, dihydroindole, indazole, purine, quinolizine, isoquinoline, quinoline, phthalazine, naphthylpyridine, quinoxaline, quinazoline, cinnoline, pteridine, carbazole, carboline, phenanthridine, acridine, phenanthroline, isothiazole, phenazine, isoxazole, phenoxazine, phenothiazine, imidazolidine, imidazoline, piperidine, piperazine, indoline, phthalimide, 1,2,3,4- tetrahydroisoquinoline,
• Niro refers to the group -NO 2 .
• Spirocyclyl refers to divalent saturated cyclic group from 3 to 10 carbon atoms having a cycloalkyl or heterocyclyl ring with a spiro union (the union formed by a single atom which is the only common member of the rings) as exemplified by the following structure:
• Sulfonyl refers to the divalent group -S(O) 2 -.
• Substituted sulfonyl refers to the group -SO 2 -alkyl, -SO 2 -substituted alkyl, -SO 2 - alkenyl, -SO 2 -substituted alkenyl, -SO 2 -cycloalkyl, -SO 2 -substituted cylcoalkyl, -SO 2 - cycloalkenyl, -SO 2 -substituted cylcoalkenyl, -SO 2 -aryl, -SO 2 -substituted aryl, -SO 2 -heteroaryl, -S ⁇ 2 -substituted heteroaryl, -SCVheterocyclic, -S ⁇ 2 -substituted heterocyclic, wherein alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkyn
• Sulfonyloxy refers to the group -OSO 2 -alkyl, -OSO 2 -substituted alkyl, -OSO 2 -alkenyl, -OSO 2 -substituted alkenyl, -OSO 2 -cycloalkyl, -OSO 2 -substituted cylcoalkyl, -OSO 2 - cycloalkenyl, -OSO 2 -substituted cylcoalkenyl,-OSO 2 -aryl, -OSO 2 -substituted aryl, -OSO 2 - heteroaryl, -OS ⁇ 2 -substituted heteroaryl, -OS ⁇ 2 -heterocyclic, -OS ⁇ 2 -substituted heterocyclic, wherein alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl
• Thioacyl refers to the groups H-C(S)-, alkyl-C(S)-, substituted alkyl-C(S)-, alkenyl-C(S)-, substituted alkenyl-C(S)-, alkynyl-C(S)-, substituted alkynyl-C(S)-, cycloalkyl-C(S)-, substituted cycloalkyl-C(S)-, cycloalkenyl-C(S)-, substituted cycloalkenyl-C(S)-, aryl-C(S)-, substituted aryl-C(S)-, heteroaryl-C(S)-, substituted heteroaryl-C(S)-, heterocyclic-C(S)-, and substituted heterocyclic-C(S)-, wherein alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, substituted
• Alkylthio refers to the group -S-alkyl wherein alkyl is as defined herein.
• Substituted alkylthio refers to the group -S-(substituted alkyl) wherein substituted alkyl is as defined herein.
• protected or a "protecting group” with respect to hydroxyl groups, amine groups, and sulfhydryl groups refers to forms of these functionalities which are protected from undesirable reaction with a protecting group known to those skilled in the art such as those set forth in Protective Groups in Organic Synthesis, Greene, T.W. , Solon Wiley & Sons, New York, NY, (1st Edition, 1981) which can be added or removed using the procedures set forth therein.
• Examples of protected hydroxyl groups include, but are not limited to, silyl ethers such as those obtained by reaction of a hydroxyl group with a reagent such as, but not limited to, t- butyldimethyl-chlorosilane, trimethylchlorosilane, triisopropylchlorosilane, triethylchlorosilane; substituted methyl and ethyl ethers such as, but not limited to methoxymethyl ether, methythiomethyl ether, benzyloxymethyl ether, t- butoxymethyl ether, 2- methoxyethoxymethyl ether, tetrahydropyranyl ethers, 1-ethoxyethyl ether, allyl ether, benzyl ether; esters such as, but not limited to, benzoylformate, formate, acetate, trichloroacetate, and trifluoracetate.
• a reagent such as, but not limited to
• protected amine groups include, but are not limited to, benzyl or dibenzyl, amides such as, fonnamide, acetamide, trifluoroacetamide, and benzamide; imides, such as phthalimide, BOC (tBoc), FMOC, and dithiosuccinimide; and others.
• a protecting group for amines is an FMOC group.
• protected sulfhydryl groups include, but are not limited to, thioethers such as S-benzyl thioether, and S-4-picolyl thioether; substituted S-methyl derivatives such as hemithio, dithio and aminothio acetals; and others.
• Stereoisomer or “stereoisomers” refer to compounds that differ in the chirality of one or more stereocenters. Stereoisomers include enantiomers and diastereomers.
• affinity refers to the strength of the binding interaction of two molecules, such as a metal-chelating compound and a metal ion.
• detectable response refers to an occurrence of, or a change in, a signal that is directly or indirectly detectable either by observation or by instrumentation.
• the detectable response is an optical response resulting in a change in the wavelength distribution patterns or intensity of absorbance or fluorescence or a change in light scatter, fluorescence lifetime, fluorescence polarization, or a combination of these parameters.
• the detectable response is an occurrence of a signal wherein the dye is inherently fluorescent and does not produce a change in signal upon binding to a metal ion or phosphorylated target molecule.
• the detectable response is the result of a signal, such as color, fluorescence, radioactivity or another physical property of the detectable label becoming spatially localized in a subset of a sample such as in a gel, on a blot, or an array, in a well of a micoplate, in a microfluidic chamber, or on a microparticle as the result of formation of a ternary complex of the invention that comprises a phosphorylated target molecule.
• a signal such as color, fluorescence, radioactivity or another physical property of the detectable label becoming spatially localized in a subset of a sample such as in a gel, on a blot, or an array, in a well of a micoplate, in a microfluidic chamber, or on a microparticle as the result of formation of a ternary complex of the invention that comprises a phosphorylated target molecule.
• enzyme refers to a protein molecule produced by living organisms, or through chemical modification of a natural protein molecule, that catalyzes chemical reaction of other substances without itself being destroyed or altered upon completion of the reactions.
• other substances include, but are not limited to chemiluminescent, chromogenic and fluorogenic substances or protein-based substrates.
• kinase sensor refers to a compound or composition capable of detecting and/or measuring kinase activity, or a precursor thereof.
• fluorophore refers to a composition that is inherently fluorescent or demonstrates a change in fluorescence upon binding to a biological compound or metal ion, i.e., fluorogenic. Fluorophores may contain substitutents that alter the solubility, spectral properties or physical properties of the fluorophore.
• fluorophores include, but are not limited to coumarin, cyanine, benzofuran, a quinoline, a quinazolinone, an indole, a benzazole, a borapolyazaindacene and xanthenes including fluoroscein, rhodamine and rhodol as well as other fluorophores described in RICHARD P. HAUGLAND, MOLECULAR PROBES HANDBOOK OF FLUORESCENT PROBES AND RESEARCH CHEMICALS (9 th edition, CD-ROM, September 2002).
• linking refers to a divalent moiety capable of linking two particles, either as a single covalent bond or a series of stable covalent bonds incorporating 1-30 nonhydrogen atoms selected from the group consisting of C, N, O, S and P that covalently attach the fluorophore, quinoline group and amino acids to form the present kinase sensor.
• exemplary linking members include a moiety that includes -C(O)NH-, -C(O)O-, -NH-, -S-, -O-, and the like.
• linkers include covalent bonds, amino acids, succinimidyl derivatives, methines, and alkenyl groups, alkyl and substituted alkyl groups, ethyleyene, proypylene, polyethylene, and polypropylene glycols, esters, ethers, amides, carbamates, and carbonyl containing moieties, diones, squarate, adipic acid as well as other groups, such as those described in Chemistry of Protein Conjugation and Cross-Linking by Susan Wong.
• a "cleavable linker” is a linker that has one or more cleavable groups that may be broken by the result of a reaction or condition.
• the term “cleavable group” refers to a moiety that allows for release of a portion, e.g., a reporter molecule, carrier molecule or solid support, of a conjugate from the remainder of the conjugate by cleaving a bond linking the released moiety to the remainder of the conjugate. Such cleavage is either chemical in nature, or enzymatically mediated.
• Exemplary enzymatically cleavable groups include natural amino acids or peptide sequences that end with a natural amino acid.
• cleaved groups include, but are not limited to, acids, bases, light (e.g., nitrobenzyl derivatives, phenacyl groups, benzoin esters), and heat.
• cleaveable groups are known in the art. See, for example, Jung et al., Biochem. Biophys. Acta, 761: 152-162 (1983); Joshi et al., J. Biol. Chem., 265: 14518-14525 (1990); Zarling et al., J.
• An exemplary cleavable group, an ester is cleavable group that may be cleaved by a reagent, e.g. sodium hydroxide, resulting in a carboxylate-containing fragment and a hydroxyl- containing product.
• a reagent e.g. sodium hydroxide
• conjugated refers to association of groups through bonds such as covalent, hydrophobic, ionic, disulfide, hydrogen, Van der Waals forces, electrostatic interactions and the like.
• conjugated refers to covalent attachment either directly or through a linker moiety.
• metal chelator or "metal-chelating moiety” as used herein refers to a chemical moiety that combines with a metal ion to form a chelate ring structure.
• the metal chelator has affinity for a metal ion that has simultaneous affinity for the metal chelator and a phosphate group on a serine, threonine, or tyrosine residue.
• the metal chelators are optionally substituted by substituents that adjust the ion-binding affinity, solubility, spectral properties or other physical properties of the compound provided that the metal chelator is not sulfonated.
• metal ion refers to any metal ion that has simultaneous affinity for a phosphorylated serine, threonine, or tyrosine on the kinase substrate and a metal-chelating compound of the invention and that can be used to form a ternary complex of the metal chelating moiety of the kinase sensor and the phosphorylated kinase substrate of the kinase sensor.
• Such metal ions include, without limitation, Ca 2+ , Zn 2 ⁇ , Mg 2+ , Ga 3+ , Tb 3 ⁇ , La 3+ , Pb 2+ , Hg 2+ , Cd 2+ , Cu 2+ , Ni , Co , Fe , Mn , Ba , and Sr .
• Particularly relevant are those metal ions that are present in biological systems such as those selected from the group consisting of Ca 2+ , Mg 2+ , Fe 2+ and Zn 2+ .
• the present compounds are used to bind Mg 2+ .
• peptide is used herein to refer to polypeptides having less than 100 amino acid residues, typically less than 20 amino acid residues.
• the terms apply to amino acid polymers in which one or more amino acid residues are an artificial chemical analogue of a corresponding naturally occurring amino acid, as well as to naturally occurring amino acid polymers.
• sample refers to any material that may contain an analyte for detection or quantification.
• the analyte may include a reactive group, e.g., a group through which a compound of the invention can be conjugated to the analyte.
• the sample may also include diluents, buffers, detergents, and contaminating species, debris and the like that are found mixed with the target.
• Illustrative examples include urine, sera, blood plasma, total blood, saliva, tear fluid, cerebrospinal fluid, secretory fluids from nipples and the like.
• the sample is a live cell, a biological fluid that comprises endogenous host cell proteins, nucleic acid polymers, nucleotides, oligonucleotides, peptides and buffer solutions.
• the sample may be in an aqueous solution, a viable cell culture or immobilized on a solid or semi solid surface such as a polyacrylamide gel, membrane blot or on a microarray.
• kinase substrates will first be described in detail, followed by the many and varied methods in which the kinase substrates can be used to detect kinase activity, which is followed by exemplified methods.
• the present invention provides kinase sensors that comprise a metal chelator, one or more amino acids and a fluorophore, wherein the fluorophore and one or more amino acids are conjugated to the metal chelating moiety.
• U.S. Patent No. 6,906,104 describes sulfonamide substituted quinoline compounds which function as kinase sensors. These compounds comprise an amino acid and the quinoline moiety, which functions as both the chelator and fluorophore.
• the present compounds comprise a fluorophore, a metal chelator such as a quinoline moiety and an amino acid.
• the fluorescence quenching effect is relieved when the kinase senor comprises a kinase substrate such that after phosphorylation a metal ion can be bound between the phosphaste group and the chelating moiety.
• the present compounds are of reduced fluorescence or essentially non- fluorescent, or fiuorogenic, until after phosphorylation by a kinase enzyme and coordinated by a metal ion.
• the term metal chelator is used as it is in the art. Namely, a metal chelator is a compound that can form two or more coordination bonds with metal ion.
• coordination bond is also well known in the art and is used to indicate a coordinate covalent bond between the metal ion and the chelator.
• the present metal-chelating moieties are moieties that simultaneously bind metal ions and have affinity for exposed phosphate groups on serine, threonine, or tyrosine residues of the kinase substrate, wherein a ternary complex is formed between the metal-chelating moiety, the metal ion and the phosphorylated serine, threonine, or tyrosine residues.
• Metal ions that have been found to bind phosphate groups include Ca 2+ , Zn 2+ , Mg 2+ , Ga 3+ , Tb 3+ , La 3+ , Pb 2+ , Hg 2+ , Cd 2+ , Cu 2+ , Ni 2+ , Co 2+ , Fe 2+ , Mn 2+ , Ba 2+ , and Sr 2+ .
• the metal-chelating moieties must 1) bind metal ions that have affinity for phosphate groups, 2) not interfere with the binding of the metal ion for the phosphate groups and 3) maintain a stable ternary complex.
• Metal-chelating moieties that fit these three criteria include quinoline or a derivative thereof, phenanthrolines or deriviatives thereof, BAPTA, IDA, DTPA and derivatives thereof.
• the present kinase sensor is represented by the following formula:
• R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are independently a fluorophore, H, alkyl, substituted alkyl, alkoxy, substituted alkoxy, acyl, acylamino, acyloxy, amino, substituted amino, aminocarbonyl, aminothiocarbonyl, aminocarbonylamino, aminothiocarbonylamino, aminocarbonyloxy, aminosulfonyl, aminosulfonyloxy, aminosulfonylamino, amidino, carboxyl, carboxyl ester, (carboxyl ester)amino, (carboxyl ester)oxy, cyano, halo, hydroxy, nitro, SO 3 H, sulfonyl, substituted sulfonyl, sulfonyloxy, thioacyl, thiol, alkylthio, substituted alkylthio, aryl, substituted ary
• R 7 and R 8 are independently H, alkyl, substituted alkyl, carbonyl, peptide or FMOC; and L is a linker; and Y is a peptide or H; n is 1-5; or a tautomer, stereoisomer, or salt thereof.
• the present fluorophores can be any fluorophore known in the art that when conjugated to a chelating moiety are fluorescent or essentially non- fluorescent.
• a fluorophore of the present invention is any chemical moiety that exhibits an absorption maximum beyond 280 nm, that when part of a kinase sensor compound retains its unique spectral properties to provide a detectable signal.
• fluorophores examples include, but are not limited to; a pyrene, an anthracene, a naphthalene, an acridine, a stilbene, an indole or benzindole, an oxazole or benzoxazole, a thiazole or benzothiazole, a 4-amino-7-nitrobenz-2- oxa-1, 3-diazole (NBD), a carbocyanine (including any corresponding compounds in US Serial Nos. 09/557,275; 09/968,401 and 09/969,853 and US patent Nos.
• oxazines include resorufms (including any corresponding compounds disclosed in 5,242,805), aminooxazinones, diaminooxazines, and their benzo-substituted analogs.
• the fluorophore of the present invention is selected from the group consisting of acridine, anthracene, benzofuran, indole, dansyl, cyanine, borapolyazaindacene, pyrene, naphthalene, coumarin, oxazine, boron dipyromethene difluoride, and xanthenes, including but not limited to fluorescein, rhodamine, and rhodol, and derivatives thereof Additional fluorophores that may be used in the present invention are listed in Richard P. Haugland, Molecular Probes Handbook of Fluorescent Probes and Research Chemicals (9 th Ed.),.
• the xanthenes are fluorescein, or rhodamine.
• the fluorophores may be substituted to adjust solubility, spectral or other physical properties.
• the fluorophore is a xanthene
• the fluorophore may, but need not be, a fluorescein, a rhodol (including any corresponding compounds disclosed in US Patent Nos. 5,227,487 and 5,442,045), a rosamine or a rhodamine (including any corresponding compounds in US Patent
• fluorescein includes benzo- or dibenzofluoresceins, seminaphthofluoresceins, or naphtho fluoresceins.
• rhodol includes seminaphthorhodafluors (including any corresponding compounds disclosed in U.S. Patent No. 4,945,171). Fluorinated xanthene fluorophores have been described previously as possessing particularly useful fluorescence properties (Int. Publ. No. WO 97/39064 and U.S. Patent No. 6,162,931) including those sold under the tradename OREGON GREEN.
• the Oregon Green precursor will allow for strategic placement of a very bright and highly absorbing pH-insensitive fluorescein derivative in peptide kinase substrates.
• the fluorescence will initially be quenched via PET by the 8-hydroxyquinoline moiety, but chelation induced fluorescence increase, mediated by magnesium(II) ion will be observed upon phosphorylation of the appropriate Ser/Thr/Tyr residue that is separated from the dye by a beta- turn dipeptide or other peptide sequence.
• the fluorescence (490 nm excitation/520 nm emission) increase will be similar in mechanism and magnitude to that observed upon using Fluo-4 for calcium measurements.
• the fluorophore-substituted amino acid is placed two amino acid residues away from the serine to be phosphorylated so that the metal chelating portion of the Oregon Green alanine derivative can be oriented toward the phosphoserine moiety.
• the hydroxyquinoline-fluorophore moiety is constructed so that the fluorescence is quenched in the absence of metal ion chelation, and the hydroxy quinoline-amino acid connection point is also chosen for optimal geometry.
• the fluorophore will contain one or more aromatic or heteroaromatic rings, that are optionally substituted one or more times by a variety of substituents, including without limitation, halogen, nitro, sulfo, cyano, alkyl, perfluoroalkyl, alkoxy, alkenyl, alkynyl, cycloalkyl, arylalkyl, acyl, aryl or heteroaryl ring system, benzo, or other substituents typically present on chromophores or fluorophores known in the art.
• substituents including without limitation, halogen, nitro, sulfo, cyano, alkyl, perfluoroalkyl, alkoxy, alkenyl, alkynyl, cycloalkyl, arylalkyl, acyl, aryl or heteroaryl ring system, benzo, or other substituents typically present on chromophores or fluorophores known in the art.
• the fluorophores are independently substituted by substituents selected from the group consisting of hydrogen, halogen, amino, substituted amino, alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxy, sulfo, reactive group and carrier molecule.
• the xanthene fluorophores of this invention comprise both compounds substituted and unsubstituted on the carbon atom of the central ring of the xanthene by substituents typically found in the xanthene-based fluorophores such as phenyl and substituted-phenyl moieties.
• the fluorophores used in the amino acids and compositions of the present invention are rhodamine, fluorescein, dansyl, naphthalene and derivatives thereof.
• the choice of the fluorophore attached to the chelating moiety will determine the absorption and fluorescence emission properties of the amino acids and compositions of the present invention as well as its live cell properties.
• Selected sulfonated fluorophores also exhibit advantageous properties, and include sulfonated pyrenes, coumarins, carbocyanines, and xanthenes (as described in U.S. Patent Nos. 5,132,432; 5,696,157; 5,268,486; 6,130,101). Sulfonated pyrenes and coumarins are typically excited at wavelengths below about 450 nm (US Patent Nos. 5,132,432 and 5,696,157).
• the label is a fluorophore selected from the group consisting of fluorescein, coumarins, rhodamines, 5 -TMRIA (tetramethylrhodamine-5-iodoacetamide), (9- (2(or4)-(N-(2-maleimdylethyl)-sulfonamidyl)-4(or 2)-sulfophenyl)-2,3 ,6,7, 12,13,16,17- octahydro-(lH,5H,l lH,15H-xantheno(2,3,4-ij:5,6,7-i'j')diquinolizin-18-ium salt) (Texas Red®), 2-(5-(l-(6-(N-(2-maleimdylethyl)-amino)-6-oxohexyl)-l,3-dihydro-3,3-dimethyl-5-sulfo-2H- indo
• fluorophore
• the amino acids and compositions of the present invention must be able to chelate a metal ion, via the chelator constituent, and metal chelation must be capable of modulating the fluorescence of the fluorophore constituent.
• the fluorophore and the chelator constituents of the amino acids and compositions of the present invention must be distinct from each other. As used herein, constituents are distinct from one another when, taken individually, each constituent is inherently capable of performing its respective function. For example, the fluorophores of the present invention are fluorescent when not comprising a portion of the amino acids or compositions of the present invention.
• the chelator constituents of the compositions are capable of chelating metals when not comprising a portion of the amino acid or compositions of the present invention.
• the chelator can modulate the fluorescence quantum yield or excitation and/or emission wavelengths of the fluorophore.
• Scheme 1 provides an illustration of a ternary complex comprising a kinase sensor of the present invention:
• the ternary complex modifies the emission and/or excitation spectrum of the kinase sensor, such that phophorylation of the peptide can be detected and/or quantified.
• the present kinase sensors comprise one or more amino acids.
• the amino acids form a peptide that comprise at least one kinase recognition motif, wherein the kinase recognition motifs comprise at least one phosphorylatable amino acid residue.
• Any kinase recognition motif can be used in accordance with the present invention.
• Recognition sequences with acidic residues may show a lesser magnitude of fluorescence increase upon phosphorylation than comparable sequences, as the affinity of the unphosphorylated peptide for magnesium tends to increase under acidic conditions.
• Phosphorylation sites within the kinase recognition motif accordance with the present invention include, but are not limited to, amino acids comprising hydroxyl groups. Examples include, but are not limited to, naturally occurring hydroxyl-containing amino acid residues, such as serine, threonine and tyrosine, as well as non-naturally occurring hydroxyl-containing amino acid residues.
• Examples of recognition motifs which can be monitored for phosphorylation using the metal binding amino acids include but are not limited to motifs recognized by the AGC (cAMP- dependent protein kinase[PKA]/protein kinaseG/protein kinase C [PKC]), the CAMK (calmodulin-dependent protein kinase), the CDK/MAPK/GSK3/CLK (CMGC), the tyrosine kinase (TK), the tyrosone kinase-like (TKL), the STE and the casein kinase 1 (CKl) groups of protein kinases, which also include their respective families and subfamilies.
• AGC cAMP- dependent protein kinase[PKA]/protein kinaseG/protein kinase C [PKC]
• CAMK calmodulin-dependent protein kinase
• CMGC CDK/MAPK/GSK3/CLK
• TK tyrosine kina
• kinase recognition motifs include, but are not limited to, at least the motifs listed in Table I, herein, and those motifs described in Table I of Pinna, L. and Donella- Deana, A., Biochimica et Biophysica Acta, 1222:415-431 (1994), which is incorporated by reference.
• the amino acid of the present invention is separated by at least one additional spacer amino acid from the phosphorylatable amino acid in the kinase recognition motif.
• the fluorescent chelating amino acid of the present invention is separated from the phosphorylatable amino acid in the kinase recognition motif by 2, 3, 4, 5, 6, 7, 8, 9, 10 or more amino acids.
• the fluorescent chelating amino acid of the present invention is separated from the phosphorylatable amino acid in the kinase recognition motif by 2 amino acid spacer residues.
• the spacer residues are used to separate and orient the fluorescent chelator amino acid towards the phosphorylatable amino acid residue contained in the kinase recognition motif.
• the spacer amino acids can be any amino acid, both natural and non-natural.
• the spacer amino acids are selected from the group consisting of proline, glycine, alanine, valine, phenylalanine, praline, methionine, isoleucine and leucine.
• the spacer amino acids are proline and at least one additional amino acids are selected from the group consisting of proline, glycine, alanine, valine, phenylalanine, praline, methionine, isoleucine and leucine.
• the spacer amino acids are proline and glycine.
• spacer amino acids that can be used to separate and orient the fluorescent chelator amino acid towards the phosphorylatable amino acid residue include ⁇ -turn sequences, ⁇ -turn sequences are well known in the art and can be used in accordance with the present invention.
• the peptides of the present invention comprise the fluorescent chelator amino acid(s), a kinase recognition motif and at least one cell-penetrating peptide sequence.
• Cell-penetrating peptides are a loosely defined class of peptides that can enter eukaryotic cells without causing membrane damage.
• CPPs include "protein transduction domains" that are well known and responsible for permitting such proteins as HIV-I Tat, antennapedia and HCV-I VP22 to traverse a cell membrane. Additional examples of CPPs include, but are not limited to, the TPlO peptide and pVEC, as well as those additional CPPs disclosed in Green, M. and Lowenstein, P.M., Cell, 55:1179-1188 (1988), which is incorporated by reference.
• the present invention also relates to methods of determining levels of kinase activity in a sample. Specifically, the methods comprising measuring the fluorescent of a peptide of the present invention, wherein the peptide comprises a fluorescent amino acid chelator and kinase recognition motif with a phosphorylation site to generate a baseline measurement. After a baseline is established, the peptide is then contacting with Mg + , a phosphate source and a kinase. After contact, the fluorescence of the peptide is then measured. A difference, if any, in fluorescence of the peptide between the non-contacted and contacted states is then determined. A difference in fluorescence can indicate the presence and/or quantity of kinase activity.
• sample refers to any material that may contain metal ions, as defined above.
• the sample is a live cell or a biological fluid that comprises endogenous host cell proteins or foodstuff or an environmental sample such as a water sample.
• biological samples to be assayed include, but are not limited to, blood, plasma, serum, urine, saliva, milk, seminal plasma, synovial fluid, interstitial fluid, cerebrospinal fluid, lymphatic fluids, bile, and amniotic fluid, tissue culture medium, tissue homogenates, cell lysates and chemical solutions.
• the scope of the methods of the present invention should not be limited by the type of sample assayed.
• the sample may be in an aqueous solution, a viable cell culture or immobilized on a solid or semi solid surface such as a polyacrylamide gel, membrane blot or on a microarray.
• the samples may or may not have been removed from their native environment.
• the portion of sample assayed need not be separated or removed from the rest of the sample or from a subject that may contain the sample.
• the sample may also be removed from its native environment.
• the sample may be processed prior to being assayed.
• the sample may be diluted or concentrated; the sample may be purified and/or at least one compound, such as an internal standard, may be added to the sample.
• the sample may also be physically altered (e.g.
• Processing also includes freezing and/or preserving the sample prior to assaying, extracting secreted cellular products from surrounding medium, or physical disruption of cells and/or tissue to actively extract the analyte of interest.
• the fluorescence measurement can be any quality of the fluorescent light, including but not limited to intensity, excitation or emission wavelength, distribution of fluorescence, fluorescence lifetime, fluorescence polarization, or a combination thereof.
• the detectable optical response upon binding a target ion is a change in fluorescence intensity that is greater than approximately 120% relative to the same compound in the absence of the metal ion, more preferably greater than 5-fold, and most preferably more that 10-fold.
• the detectable optical response upon binding the target metal ion is a shift in either the maximal excitation or emission wavelength or both that is greater than about 20 nm, more preferably greater than about 50 nm.
• the instant metal ion- binding compounds are particularly useful in the formulation of a kit for the complexation, detection, quantification or monitoring of selected target ions, comprising one or more compounds or compositions of the invention in any of the embodiments described above (optionally in a stock solution), instructions for the use of the compound to complex or detect a desired target ion, and optionally comprising additional components.
• the compounds of the invention are associated with a surface, such as a chip, microplate well, or other solid matrix, and the sample of interest flows over the surface. The detectable optical response is therefore detected on the matrix surface itself.
• a kit of the present invention for binding a target metal ion in a sample comprises a present compound and instructions for use thereof.
• the kit may further comprise one or more components selected from the group consisting of a calibration standard of a metal ion, an ionophore, a fluorescent standard, an aqueous buffer solution and an organic solvent.
• the additional kit components may be selected from, without limitation, calibration standards of a target ion, ionophores, fluorescence standards, aqueous buffers, and organic solvents.
• the additional kit components are present as pure compositions, or as aqueous solutions that incorporate one or more additional kit components. Any or all of the kit components optionally further comprise buffers.
• the freed aliphatic amino group is protected as a fluorenoxymethylenecarbonyl carbamate, followed by condensation of the benzaldehyde moiety with two equivalents of 4-fluororesorcinol in methanesulfonic acid at rt.
• the resulting pro- fluorophore G is isolated by precipitation from water and filtration, followed by dehydrogenative oxidation with p-choranil in methane/chloroform.
• the resulting dye H is purified by flash chromatography using methanol in chloroform as eluant, and then readied for peptide synthesis of allyl ester deprotection using sodium 2-ethylhexanoate and catalytic Pd(PPli3) 4 in ethyl acetate and dichloromethane to give compound I.
• Peptides are synthesized using standard Fmoc amino acid protection chemistry on Fmoc-PAL- PEG-PS resin (0.22 mmol equiv.). Couplings of Fmoc-protected amino acids to the resin are carried out with 1-benzotriazolyoxytris (pyrrolidino) phophonium hexafluorophosphate (PyBOP), 1-hydroxybenzotriazole (H. OBt) and diisopropylethylamine (DIEA) or 0-(7- azabenzotrazol-l-yl)-l,l,33-tetramethyl uranium hexafluorophosphate (HATU) and DIEA to generate the activated ester.
• 1-benzotriazolyoxytris pyrrolidino) phophonium hexafluorophosphate
• H. OBt 1-hydroxybenzotriazole
• DIEA diisopropylethylamine
• HATU
• the resin is swelled in dichloromethane (5 min.) then DMF (5 min.) prior to synthesis. All amino acids other than the fluorescent chelator, phosphoserine, phospho threonine and phosphotyrosine are added by the following representative procedure: removal of the Fmoc group (20% piperidine solution in DMF, 3.times.5 min.), wash (DMF, 5.times.l min.), coupling (amino acid/PyBOP/DIEA, 6:6:6, 0.05 M in DMF, 45 min.), rinse (DMF, 2.times.l min; DCM, 2.times.l min.).
• the peptide is acetyl-capped (pyridine/acetic anhydride, 20:20, 0.15 M in DMF, 30 min.), and a final deblock cycle (20% piperidine in DMF, 3.times.5 min.) is performed to cleave any aryl ester formed on the fluorescent chelator.
• the resin is dried under high vacuum overnight prior to a 2.5 -hour cleavage with trifluoroacetic acid/triisopropylsilane/water (95:2.5:2.5, 40 ml/mg resin for unphosphorylated peptides and 140 ml/mg resin for phosphorylated peptides).
• PKC On the day of the assay, a 1 ⁇ l aliquot of Protein Kinase C ⁇ (Human, Recombinant, Calbiochem) is diluted with 20 ⁇ l of solution of 20 mM HEPES pH 7.4 containing 12.5 MM MgCI 2 and 0.38 mM CaCl2 and stored on ice.
• a typical reaction contains solution of 20 mM HEPES pH 7.4 containing 12.5 MM MgCI 2 and 0.38 mM CaCl 2 (84 ⁇ l), solution of 20 mM HEPES pH 7.4 with 5 mM dithiothreitol (19 ⁇ l ), solution of 10 ⁇ g/ml phosphatidylserine and 2 ⁇ g/ml diacylglycerol in 20 mM HEPES pH 7.4 (5 ⁇ l), solution of 100 mM ATP dissolved in ultrapure (18 M ⁇ ) water (1 ⁇ l), and enzyme working stock (1 ⁇ l). An appropriate volume of substrate stock solution is added to begin the reaction.
• PKA On the day of the assay, a 1 ⁇ l aliquot of c AMP-dependent Protein Kinase (Catalytic Subunit, Mouse, Recombinant, Calbiochem) is diluted with 80 ⁇ l of 50 mM TRIS pH 7.5 containing 10 mM MgC12 and 0.3 mg/ml BSA and maintained on ice.
• a typical reaction contains a solution of 20 mM HEPES pH 7.4 containing 12.5 mM MgCl 2 (90 ⁇ l), solution of 20 mM HEPES pH 7.4 with 5 mM dithiothreitol (20 ⁇ l), solution of 100 mM ATP dissolved in ultrapure (18 M ⁇ ) water (1 ⁇ l) and an appropriate volume of substrate stock solution. Enzyme working stock (1 ⁇ l) was added to begin the reaction.
• Fluorescence experiments are performed on a Fluoromax 3 from Jobin Yvon. 5 nm emission and excitation slit widths are used. Excitation wavelengths that match the absorption maxima of the fluorescent amino acids in the peptide are used. Enzyme assays are performed by monitoring emission at the fluorophore emission maximum wavelength. As a control, standard curves for the phosphopeptide and the non-phosphopeptide can be constructed by making serial dilutions of each stock and recording the relative fluorescent units (RFUs).
• REUs relative fluorescent units

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