Literature DB >> 22065224

Affinity-based profiling of dehydrogenase subproteomes.

Xia Ge1, Daniel S Sem.   

Abstract

The high cost of drug discovery and development requires more efficient approaches to the identification and inhibition of tractable protein targets. One strategy is to pursue families of proteins that already possess affinity for a drug lead scaffold, where that scaffold plays the dual role of serving (a) when tethered to a resin, as a ligand to purify a subproteome of interest, and (b) as a lead molecule that has the potential for optimization for a given member of the subproteome. Here, we describe an example of the purification of a subproteome using a scaffold tailored to the dehydrogenase family of enzymes. Combined with modern LC-MS/MS methods and subsequent searching of proteome databases, such affinity chromatography strategies can be used to purify and identify any proteins with affinity for the scaffold molecule. The method is exemplified using the CRAA (catechol rhodanine acetic acid) privileged scaffold, which is tailored to dehydrogenases. CRAA affinity column chromatography, combined with LC-MS/MS, is described as a method for profiling dehydrogenase subproteomes.

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Year:  2012        PMID: 22065224      PMCID: PMC4092038          DOI: 10.1007/978-1-61779-364-6_11

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  23 in total

1.  Systems-based design of bi-ligand inhibitors of oxidoreductases: filling the chemical proteomic toolbox.

Authors:  Daniel S Sem; Bonnie Bertolaet; Brian Baker; Edcon Chang; Aurora D Costache; Stephen Coutts; Qing Dong; Mark Hansen; Victor Hong; Xuemei Huang; Richard M Jack; Richard Kho; Henk Lang; Chen-Ting Ma; David Meininger; Maurizio Pellecchia; Fabrice Pierre; Hugo Villar; Lin Yu
Journal:  Chem Biol       Date:  2004-02

Review 2.  Chemical proteomics applied to target identification and drug discovery.

Authors:  Steven H L Verhelst; Matthew Bogyo
Journal:  Biotechniques       Date:  2005-02       Impact factor: 1.993

Review 3.  Chemical and pathway proteomics: powerful tools for oncology drug discovery and personalized health care.

Authors:  Ulrich Kruse; Marcus Bantscheff; Gerard Drewes; Carsten Hopf
Journal:  Mol Cell Proteomics       Date:  2008-08-01       Impact factor: 5.911

4.  Affinity chromatography of nicotinamide nucleotide-dependent dehydrogenases on immobilized nucleotide derivatives.

Authors:  I P Trayer; H R Trayer
Journal:  Biochem J       Date:  1974-09       Impact factor: 3.857

5.  Simple chemical synthesis of a specific effector for the affinity chromatography of nicotinamide adenine dinucleotide phosphate-dependent dehydrogenases.

Authors:  A Morelli; U Benatti
Journal:  Ital J Biochem       Date:  1974 Sep-Oct

6.  Aldose reductase structures: implications for mechanism and inhibition.

Authors:  O El-Kabbani; F Ruiz; C Darmanin; R P-T Chung
Journal:  Cell Mol Life Sci       Date:  2004-04       Impact factor: 9.261

Review 7.  Activity-based probes as a tool for functional proteomic analysis of proteases.

Authors:  Marko Fonović; Matthew Bogyo
Journal:  Expert Rev Proteomics       Date:  2008-10       Impact factor: 3.940

8.  Binding synergy and cooperativity in dihydrodipicolinate reductase: implications for mechanism and the design of biligand inhibitors.

Authors:  Xia Ge; Andrew Olson; Sheng Cai; Daniel S Sem
Journal:  Biochemistry       Date:  2008-08-19       Impact factor: 3.162

9.  Genome-wide profile of oxidoreductases in viruses, prokaryotes, and eukaryotes.

Authors:  Richard Kho; Joseph V Newman; Richard M Jack; Hugo O Villar; Mark R Hansen
Journal:  J Proteome Res       Date:  2003 Nov-Dec       Impact factor: 4.466

10.  Analysis of nucleoside-binding proteins by ligand-specific elution from dye resin: application to Mycobacterium tuberculosis aldehyde dehydrogenases.

Authors:  Chang-Yub Kim; Cecelia Webster; Justin K M Roberts; Jin Ho Moon; Emily Z Alipio Lyon; Heungbok Kim; Minmin Yu; Li-Wei Hung; Thomas C Terwilliger
Journal:  J Struct Funct Genomics       Date:  2009-11-13
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