Literature DB >> 17177392

Encodable activators of SRC family kinases.

Crystal D Zellefrow1, Jennifer S Griffiths, Sarmistha Saha, Abby M Hodges, Jessica L Goodman, Joshiawa Paulk, Joshua A Kritzer, Alanna Schepartz.   

Abstract

There is considerable current interest in the design of encodable molecules that regulate intracellular protein circuitry and/or activity, ideally with a high level of specificity. Src homology 3 (SH3) domains are ubiquitous components of multidomain signaling proteins, including many kinases, and are attractive drug targets because of the important role their interactions play in diseases as diverse as cancer, osteoporosis, and inflammation. Here we describe a set of miniature proteins that recognize distinct SH3 domains from Src family kinases with high affinity. Three of these molecules discriminate effectively between the SH3 domains of Src and Fyn, which are expressed ubiquitously, and two of these three activate Hck kinase with potencies that rival HIV Nef, one of the most potent kinase activators known. These results suggest that miniature proteins represent a viable, encodable strategy for selective activation of Src family kinases in a variety of cell types.

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Year:  2006        PMID: 17177392     DOI: 10.1021/ja0672977

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  5 in total

1.  Rewiring kinase specificity with a synthetic adaptor protein.

Authors:  Elissa M Hobert; Alanna Schepartz
Journal:  J Am Chem Soc       Date:  2012-02-22       Impact factor: 15.419

2.  Arginine mimetics using α-guanidino acids: introduction of functional groups and stereochemistry adjacent to recognition guanidiniums in peptides.

Authors:  Shalini Balakrishnan; Michael J Scheuermann; Neal J Zondlo
Journal:  Chembiochem       Date:  2011-12-23       Impact factor: 3.164

3.  The Abl SH2-kinase linker naturally adopts a conformation competent for SH3 domain binding.

Authors:  Shugui Chen; Sébastien Brier; Thomas E Smithgall; John R Engen
Journal:  Protein Sci       Date:  2007-02-27       Impact factor: 6.725

4.  Bivalent inhibitors of the tyrosine kinases ABL and SRC: determinants of potency and selectivity.

Authors:  Zachary B Hill; B Gayani K Perera; Dustin J Maly
Journal:  Mol Biosyst       Date:  2010-11-09

5.  Arginine topology controls escape of minimally cationic proteins from early endosomes to the cytoplasm.

Authors:  Jacob S Appelbaum; Jonathan R LaRochelle; Betsy A Smith; Daniel M Balkin; Justin M Holub; Alanna Schepartz
Journal:  Chem Biol       Date:  2012-07-27
  5 in total

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