Title
Purifying protein complexes for mass spectrometry: Applications to protein translation
Date Issued
01 January 2005
Access level
metadata only access
Resource Type
journal article
Author(s)
Vanderbilt University
Publisher(s)
Academic Press Inc.
Abstract
Proteins control and mediate most of the biological activities in the cell. In most cases, proteins either interact with regulatory proteins or function in large molecular assemblies to carryout biological processes. Understanding the functions of individual proteins requires the identification of these interacting proteins. With its speed and sensitivity, mass spectrometry has become the dominant method for identifying components of protein complexes. This article reviews and discusses various approaches to purify protein complexes and analyze the proteins using mass spectrometry. As examples, methods to isolate and analyze protein complexes responsible for the translation of messenger RNAs into polypeptides are described. © 2004 Elsevier Inc. All rights reserved.
Start page
274
End page
290
Volume
35
Issue
3 SPEC.ISS.
Language
English
OCDE Knowledge area
Bioquímica, Biología molecular
Subjects
Scopus EID
2-s2.0-13844275954
PubMed ID
Source
Methods
ISSN of the container
10462023
Sponsor(s)
We thank Dr. Kathleen L. Gould and Dr. Joe Tasto for TAP vectors and assistance with the TAP protocols. This work was supported by NIH Grant GM64779 to A.J.L. A.J.L. is supported by NIH Grants GM64779, HL68744, NS43952, ES11993, and CA098131. C.W. and J.L.J. is supported by NIH Grants GM64779 and HL68744. V.R.G. is supported by NIH training Grant T32 CA009385. T.C.F. is supported by NIH training Grant T32 AI49824.
Sources of information:
Directorio de Producción Científica
Scopus