Rapid quantitative analysis of proteins or protein function...

Chemistry: analytical and immunological testing – Nuclear magnetic resonance – electron spin resonance or other...

Reexamination Certificate

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C436S086000, C436S089000, C436S120000, C436S161000, C436S165000, C436S166000, C436S167000, C436S168000, C436S171000, C436S173000, C436S174000, C436S175000, C436S177000, C530S350000, C530S812000, C530S391500

Reexamination Certificate

active

06852544

ABSTRACT:
Analytical reagents and mass spectrometry-based methods using these reagents for the rapid, and quantitative analysis of proteins or protein function in mixtures of proteins. The methods employ affinity labeled protein reactive reagents having three portions: an affinity label (A) covalently linked to a protein reactive group (PRG) through a linker group (L). The linker may be differentially isotopically labeled, e.g., by substitution of one or more atoms in the linker with a stable isotope thereof. These reagents allow for the selective isolation of peptide fragments or the products of reaction with a given protein (e.g., products of enzymatic reaction) from complex mixtures. The isolated peptide fragments or reaction products are characteristic of the presence of a protein or the presence of a protein function in those mixtures. Isolated peptides or reaction products are characterized by mass spectrometric (MS) techniques. The reagents also provide for differential isotopic labeling of the isolated peptides or reaction products which facilitates quantitative determination by mass spectrometry of the relative amounts of proteins in different samples. The methods of this invention can be used for qualitative and quantitative analysis of global protein expression profiles in cells and tissues, to screen for and identify proteins whose expression level in cells, tissue or biological fluids is affected by a stimulus or by a change in condition or state of the cell, tissue or organism from which the sample originated.

REFERENCES:
patent: 4798795 (1989-01-01), Sigler
patent: 5240859 (1993-08-01), Aebersold
patent: 5438017 (1995-08-01), Allen et al.
patent: 5514559 (1996-05-01), Markert-Hahn et al.
patent: 5538897 (1996-07-01), Yates, III et al.
patent: 5614368 (1997-03-01), Ghazarossian et al.
patent: 5650270 (1997-07-01), Giese et al.
patent: 5686310 (1997-11-01), Haystead et al.
patent: 5952653 (1999-09-01), Covey et al.
patent: 6017693 (2000-01-01), Yates, III et al.
patent: 6057096 (2000-05-01), Rothschild et al.
patent: 6156527 (2000-12-01), Schmidt et al.
patent: 6670194 (2003-12-01), Aebersold et al.
patent: 1 027 454 (2003-08-01), None
patent: WO9826095 (1998-06-01), None
patent: 9832876 (1998-07-01), None
patent: WO9832876 (1998-07-01), None
patent: 9902726 (1999-01-01), None
patent: 9902728 (1999-01-01), None
patent: WO 0196869 (2001-12-01), None
Duncan et al., Amino acid analysis of Peptides and Proteins on femtomole scale by Gas Chromatography/Mass Spectrometry, Anal. Chem. 70: 890-896 (Mar. 1998).*
Aebersold, R. et al. (1991) “Determination of the site of tyrosine phosphorylation at the low picomole level by automated solid-phase sequence analysis”Anal. Biochem. 199:51-60.
Bennetzen, J.L. and Hall, B.D. , “Codon Selection in Yeast,” (Mar. 1982)J. Biol. Chem. 257(6):3026-3031.
Boucherie, H. et al. (1996) “Two-dimensional gel protein database ofSaccharomyces cerevisiae” Electrophoresis17:1683-1699.
Bruce, J. E. et al. (Jan. 2000) “Obtaining More Accurate FTICR Mass Measurements Without Internal Standards using Multiply Charged Ions”J. Am. Soc. Mass Spec. 11(5):416-421.
Bruce, J.E. et al. (Jul. 1999) “High-Mass-Measurement Accuracy and 100% Sequence Coverage of Enzymatically Digested Bovine Serum Albumin from an ESI-FTICR Mass Spectrum”Anal. Chem. 71(14):2595-2599.
Davis, T. et al. (Mar. 1998) “Rapid Protein Identification Using a Microscale Electrospray LC/MS System on an Ion Trap Mass Spectrometer,”J. Am. Soc. Mass. Spec. 9:194-201.
Fenyo, D. et al. (May 1998) “Protein indentification using mass spectrometric information,”Electrophoresis19:998-1005.
Fraser, C.M. et al. (Dec. 1997) “Genomic sequence of a Lyme disease spirochaete,Borrelia burgdorferi,” Nature390:580-586.
Futcher, B. et al. (Nov. 1999) “A Sampling of the Yeast Proteome”Mol. Cell. Bio. 19(11):7357-7368.
Gingras, A.C. et al. (Jun. 1999) “Regulation of 4E-BP1phophorylation: a novel two-step mechanism”Genes Dev. 13:1422-1437.
Goffeau et al. (Oct. 1996) “Life with 6000 Genes,” Science 274:546-549.
Goodlett et al. (1993), “Reduced Elution Speed Detection for Capillary Electrophoresis/Mass Spectrometry”J. Microcolumn Separations5:57-62.
Goodlett, D.R. et al. (Mar. 2000) “Protein identification with a single accurate mass of a cysteine-containing peptide and constrained database searching”Anal. Chem. 72(6):1112-1118.
Goodlett, D.R. et al. (Mar. 2000) “Quantitative in Vitro kinase reaction as a guide for phosphoprotein analysis by mass spectrometry”Rapid Commun Mass Spectrom. 14(5):344-348.
Graves, J.D. & Krebs, ED. (May 1999) “Protein phosphorylation and signal transduction”Pharmacol. Ther. 82:(2-3)111-121.
Gygi, S.P. and Aebersold, R. (Oct. 2000) “Mass spectrometry and proteomics”Curr. Opin. Chem. Biol. 4(5):489-94.
Gygi, S.P. et al. (Aug. 2000) “Measuring gene expression by quantitative proteome analysis”Curr. Opin. Biotechnol. 11(4):396-401.
Haynes, P.A. et al. (1998) “Proteome Analysis: Biological Assay or Data Archive?”Electrophoresis vol. 19:1862-1871.
Henzel, W.J. et al. (Jun. 1993) “Identifying proteins from two-dimensional gels by molecular mass searching of peptide fragments in protein sequence databases,”Proc. Natl. Acad. Sci. USA90:5011-5015.
Horn, D. M. et al. (1998) “A Computer Program for Automated Analysis of High Resolution Mass Spectra,”Proceedings of the 46thASMS Conf. on Mass Spectromety and Allied Topics, Orlando, FL May 31—Jun. 4, 1998, p. 118.
Hunter, T. (1994) “1001 protein kinases redux—towards 2000”Semin. Cell Biol. 5:367-376.
Jonscher, K.R. and Yates, J.R. III, (Jan. 1997) “Matrix-assisted laser desorption ionization/quadrupole ion trap mass spectrometry of peptides. Application to the localization of phosphorylation sites on the P protein from Sendai virus”J,. Biol. Chem. 272(3):1735-1741.
Koch, C.A. et al. (1991) “SH2 and SH3 domains: elements that control interactions of cytoplasmic signaling proteins”Science252:668-674.
Laemmli, U.K. (Aug. 1970) “Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4,”Nature227:680-695.
Lee et al. (Jan. 1998) “HLA-E Surface Expression Depends on Binding of TAP-Dependent Peptides Derived from Certain HLA Class I Signal Sequences,”J. Immunol. 160:4951-4960.
Link, J. et al. (Jul. 1999) “Direct analysis of protein complexes using mass spectrometry,”Nat. Biotech. 17:676-682.
Lundell, N. and Schreitmuller, T. (Jan. 1999) “Sample Preparation for Peptide Mapping—A Pharmaceutical Quality-Control Perspective,” Anal. Biochem.266:31-47.
Marshall et al. (May 1998) “Fourier Transform Ion Cyclotron Resonance Mass Spectrometry: A Primer,”Mass. Spectrom. Rev. 17:1-35.
McCormack, A.L. et al. (1997) “Direct Analysis and Identification of Proteins in Mixtures by LC/MS/MS and Database Searching at the Low-Femtomole Level”Anal. Chem. 69:767-776.
Mosley, M.A. et al. (1991) “Nanoscale Packed-Capillary Liquid Chromatography Coupled with Mass Spectrometry Using a Coaxial Continuous-Flow Fast Atom Bombardment Interface,”Anal. Chem. 63:1467-1473.
Neubauer, G. et al. (Sep. 1998) “Mass spectrometry and EST-database searching allows characterization of the multi-protein spliceosome complex,”Nature Genetics20:46-50.
Ogryzko, Vasily V. et al. (Jul. 10, 2998), “Histone-like TAFs within the PCAF Histone Acetylase Complex”Cell94:35-44.
Papayannopoulos, I.A. (1995) “The interpretation of collision-induced dissociation tandem mass spectra of peptides”Mass Spectrometry Rev. 14:49-73.
Patterson, S.D. and Aebersold, R. (1995) “Mass spectrometric approaches for the identification of gel-separated proteins,”Electro. 16:1791-1814.
Qin, J. et al. (Jan. 1998) “De Nov

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