Single-spanning transmembrane domains in cell growth and cell-cell interactions: More than meets the eye?

TitleSingle-spanning transmembrane domains in cell growth and cell-cell interactions: More than meets the eye?
Publication TypeJournal Article
Year of Publication2010
AuthorsHubert P, Sawma P, Duneau J-P, Khao J, Hénin J, Bagnard D, Sturgis J
JournalCell Adh. Migr.
Volume4
Pagination313–324
Date Publishedapr
ISSN1933-6926
KeywordsAnimals, Biological, Humans, Membrane Proteins, Models, Protein Structure, Secondary, Signal Transduction, Tertiary
Abstract

As a whole, integral membrane proteins represent about one third of sequenced genomes, and more than 50% of currently available drugs target membrane proteins, often cell surface receptors. Some membrane protein classes, with a defined number of transmembrane (TM) helices, are receiving much attention because of their great functional and pharmacological importance, such as G protein-coupled receptors possessing 7 TM segments. Although they represent roughly half of all membrane proteins, bitopic proteins (with only 1 TM helix) have so far been less well characterized. Though they include many essential families of receptors, such as adhesion molecules and receptor tyrosine kinases, many of which are excellent targets for biopharmaceuticals (peptides, antibodies, et al.). A growing body of evidence suggests a major role for interactions between TM domains of these receptors in signaling, through homo and heteromeric associations, conformational changes, assembly of signaling platforms, etc. Significantly, mutations within single domains are frequent in human disease, such as cancer or developmental disorders. This review attempts to give an overview of current knowledge about these interactions, from structural data to therapeutic perspectives, focusing on bitopic proteins involved in cell signaling.

DOI10.4161/cam.4.2.12430
Citation Key2010|1789