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Kuhn Lab at The Scripps Research Institute. > KSPublications > Remedial strategies in structural proteomics: Expression, purification, and crystallization of the Vav1/Rac1 complex.  

KSPublications: Remedial strategies in structural proteomics: Expression, purification, and crystallization of the Vav1/Rac1 complex.

Title

Remedial strategies in structural proteomics: Expression, purification, and crystallization of the Vav1/Rac1 complex. 

Authors

Brooun A., et al. 

Abstract

The signal transduction pathway involving the Vav1 guanine nucleotide exchange factor (GEF) and the Rac1 GTPase plays several key roles in the immune response mediated by the T cell receptor. Vav1 is also a unique member of the GEF family in that it contains a cysteine-rich domain (CRD) that is critical for Rac1 binding and maximal guanine nucleotide exchange activity, and thus may provide a unique protein-protein interface compared to other GEF/GTPase pairs. Here, we have applied a number of remedial structural proteomics strategies, such as construct and expression optimization, surface mutagenesis, limited proteolysis, and protein formulation to successfully express, purify, and crystallize the Vav1-DH-PH-CRD/Rac1 complex in an active conformation. We have also systematically characterized various Vav1 domains in a GEF assay and Rac1 in vitro binding experiments. In the context of Vav1-DH-PH-CRD, the zinc finger motif of the CRD is required for the expression of stable Vav1, as well as for activity in both a GEF assay and in vitro formation of a Vav1/Rac1 complex suitable for biophysical and structural characterization. Our data also indicate that the isolated CRD maintains a low level of specific binding to Rac1, appears to be folded based on 1D NMR analysis and coordinates two zinc ions based on ICP-MS analysis. The protein reagents generated here are essential tools for the determination of a three dimensional Vav1/Rac1 complex crystal structure and possibly for the identification of inhibitors of the Vav1/Rac1 protein-protein interaction with potential to inhibit lymphocyte activation.

Journal

Protein Expr Purif. 

Date

12/5/2006 

Link

PubMed Entry 

Reference

Brooun A, Foster SA, Chrencik JE, Chien EY, Kolatkar AR, Streiff M, Ramage P, Widmer H, Weckbecker G, Kuhn P. "Remedial strategies in structural proteomics: Expression, purification, and crystallization of the Vav1/Rac1 complex." Protein Expr Purif. 2006 Dec 5;

PMID

17275330 

Keyword

PPI 

TSRI Number

18391 
Attachments
Created at 2/23/2007 10:56 AM  by Sophie Coon 
Last modified at 2/15/2008 2:23 PM  by Elvia Nunez