Visualizing intermolecular interactions in T cells.

Abstract:

:The use of appropriate fluorescent proteins has allowed the use of FRET microscopy for investigation of intermolecular interactions in living cells. This method has the advantage of both being dynamic and of working at the subcellular level, so that the time and place where proteins interact can be visualized. We have used FRET microscopy to analyze the interactions between the T cell antigen receptor and the coreceptors CD4 and CD8. This chapter reviews data on how these coreceptors are recruited to the immunological synapse, and how they interact when the T cell is stimulated by different ligands.

authors

Gascoigne NR,Ampudia J,Clamme JP,Fu G,Lotz C,Mallaun M,Niederberger N,Palmer E,Rybakin V,Yachi PP,Zal T

doi

10.1007/978-3-540-93864-4_2

subject

Has Abstract

pub_date

2009-01-01 00:00:00

pages

31-46

eissn

0070-217X

issn

2196-9965

journal_volume

334

pub_type

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