Literature DB >> 14679191

An oriented peptide array library (OPAL) strategy to study protein-protein interactions.

Maria Rodriguez1, Shawn S-C Li, J Wade Harper, Zhou Songyang.   

Abstract

One of the major questions in signal transduction is how the specificities of protein-protein interactions determine the assembly of distinct signaling complexes in response to stimuli. Several peptide library methods have been developed and widely used to study protein-protein interactions. These approaches primarily rely on peptide or DNA sequencing to identify the peptide or consensus motif for binding and may prove too costly or difficult to accommodate high throughput applications. We report here an oriented peptide array library (OPAL) approach that should facilitate high throughput proteomic analysis of protein-protein interactions. OPAL integrates the principles of both the oriented peptide libraries and array technologies. Hundreds of pools of oriented peptide libraries are synthesized as amino acid scan arrays. We demonstrate that these arrays can be used to map the specificities of a variety of interactions, including antibodies, protein domains such Src homology 2 domains, and protein kinases.

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Year:  2003        PMID: 14679191     DOI: 10.1074/jbc.M311886200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  35 in total

1.  Loops govern SH2 domain specificity by controlling access to binding pockets.

Authors:  Tomonori Kaneko; Haiming Huang; Bing Zhao; Lei Li; Huadong Liu; Courtney K Voss; Chenggang Wu; Martin R Schiller; Shawn Shun-Cheng Li
Journal:  Sci Signal       Date:  2010-05-04       Impact factor: 8.192

2.  SH2 domains recognize contextual peptide sequence information to determine selectivity.

Authors:  Bernard A Liu; Karl Jablonowski; Eshana E Shah; Brett W Engelmann; Richard B Jones; Piers D Nash
Journal:  Mol Cell Proteomics       Date:  2010-07-13       Impact factor: 5.911

3.  Phosphorylation-dependent substrate selectivity of protein kinase B (AKT1).

Authors:  Nileeka Balasuriya; Norman E Davey; Jared L Johnson; Huadong Liu; Kyle K Biggar; Lewis C Cantley; Shawn Shun-Cheng Li; Patrick O'Donoghue
Journal:  J Biol Chem       Date:  2020-04-29       Impact factor: 5.157

Review 4.  Specificity and versatility of SH3 and other proline-recognition domains: structural basis and implications for cellular signal transduction.

Authors:  Shawn S-C Li
Journal:  Biochem J       Date:  2005-09-15       Impact factor: 3.857

5.  Defining SH2 domain and PTP specificity by screening combinatorial peptide libraries.

Authors:  Anne-Sophie Wavreille; Mathieu Garaud; Yanyan Zhang; Dehua Pei
Journal:  Methods       Date:  2007-07       Impact factor: 3.608

Review 6.  Understanding and exploiting substrate recognition by protein kinases.

Authors:  Benjamin E Turk
Journal:  Curr Opin Chem Biol       Date:  2008-03-07       Impact factor: 8.822

Review 7.  Deciphering enzyme function using peptide arrays.

Authors:  Alexandra Thiele; Gabriele I Stangl; Mike Schutkowski
Journal:  Mol Biotechnol       Date:  2011-11       Impact factor: 2.695

8.  Surface Loops in a Single SH2 Domain Are Capable of Encoding the Spectrum of Specificity of the SH2 Family.

Authors:  Huadong Liu; Haiming Huang; Courtney Voss; Tomonori Kaneko; Wen Tao Qin; Sachdev Sidhu; Shawn S-C Li
Journal:  Mol Cell Proteomics       Date:  2018-11-27       Impact factor: 5.911

9.  Engineered SH2 domains with tailored specificities and enhanced affinities for phosphoproteome analysis.

Authors:  Gianluca Veggiani; Haiming Huang; Bradley P Yates; Jiefei Tong; Tomonori Kaneko; Rakesh Joshi; Shawn S C Li; Michael F Moran; Gerald Gish; Sachdev S Sidhu
Journal:  Protein Sci       Date:  2018-12-24       Impact factor: 6.725

10.  Kinase peptide specificity: improved determination and relevance to protein phosphorylation.

Authors:  Koichi Fujii; Guozhi Zhu; Yin Liu; John Hallam; Lin Chen; Juan Herrero; Stephen Shaw
Journal:  Proc Natl Acad Sci U S A       Date:  2004-09-08       Impact factor: 11.205

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