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  Purification of the T Cell Antigen Receptor and Analysis by Blue-Native PAGE

Swamy, M., & Schamel, W. W. A. (2009). Purification of the T Cell Antigen Receptor and Analysis by Blue-Native PAGE. Methods in Molecular Biology, 514, 135-150.

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 Creators:
Swamy, Mahima1, Author           
Schamel, Wolfgang W. A.1, Author           
Affiliations:
1Research Group and Chair of Molecular Immunology of the University of Freiburg, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society, ou_2243645              

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Free keywords: T cells, T cell receptor, BN-PAGE, multi-protein complex, stoichiometry, affinity purification
 Abstract: The T cell antigen receptor (TCR) is a multi-protein complex composed of six different transmembrane subunits, which form complexes of various sizes on the surface of resting T cells. The stoichiometry of the smallest form was recently determined to be αβγεδεζζ, whereas that of the larger forms is unknown. The roles of the different forms and their ratios are poorly defined. Biochemical analyses to address these questions must focus on the detergent and the best native conditions to maintain the integrity of the complexes. Blue-native polyacrylamide gel electrophoresis (BN-PAGE) is a high-resolution native protein separation method that relies on the dye Coomassie blue to confer negative charge for separation. Using this powerful approach, the size, subunit composition and the relative abundance of the different TCR forms can be studied. We present here four methods to isolate the TCR in a native form and details to analyse it by BN-PAGE.

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Language(s): eng - English
 Dates: 2009
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 464811
 Degree: -

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Title: Methods in Molecular Biology
  Alternative Title : Meth. Mol. Biol.
Source Genre: Journal
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Pages: - Volume / Issue: 514 Sequence Number: - Start / End Page: 135 - 150 Identifier: -