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Review
. 2010 Apr-Jun;4(2):249-54.
doi: 10.4161/cam.4.2.10725. Epub 2010 Apr 23.

Receptor tyrosine kinase transmembrane domains: Function, dimer structure and dimerization energetics

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Review

Receptor tyrosine kinase transmembrane domains: Function, dimer structure and dimerization energetics

Edwin Li et al. Cell Adh Migr. 2010 Apr-Jun.

Abstract

The transmembrane (TM) domains of receptor tyrosine kinases (RTKs) play an active role in signaling. They contribute to the stability of full-length receptor dimers and to maintaining a signaling-competent dimeric receptor conformation. In an exciting new development, two structures of RTK TM domains have been solved, a break-through achievement in the field. Here we review these structures, and we discuss recent studies of RTK TM domain dimerization energetics, possible synergies between domains, and the effects of pathogenic RTK TM mutations on structure and dimerization.

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Figures

Figure 1
Figure 1
Pathogenic single amino acid mutations in RTK TM domains may affect signaling through different mechanisms.

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