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Published online before print December 22, 2006, 10.1110/ps.062494307
Protein Science (2007), 16:285-292. Published by Cold Spring Harbor Laboratory Press. Copyright © 2007 The Protein Society
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The transmembrane homotrimer of ADAM 1 in model lipid bilayers

Siok Wan Gan, Lin Xin, and Jaume Torres

School of Biological Sciences, Nanyang Technological University, Singapore 637551

(RECEIVED August 12, 2006; FINAL REVISION October 27, 2006; ACCEPTED November 1, 2006)

Fertilin is a transmembrane protein heterodimer formed by the two subunits fertilin {alpha} and fertilin beta that plays an important role in sperm–egg fusion. Fertilin {alpha} and beta are members of the ADAM family, and contain each one transmembrane {alpha}-helix, and are termed ADAM 1 and ADAM 2, respectively. ADAM 1 is the subunit that contains a putative fusion peptide, and we have explored the possibility that the transmembrane {alpha}-helical domain of ADAM 1 forms homotrimers, in common with other viral fusion proteins. Although this peptide was found to form various homooligomers in SDS, the infrared dichroic data obtained with the isotopically labeled peptide at specific positions is consistent with the presence of only one species in DMPC or POPC lipid bilayers. Comparison of the experimental orientational data with molecular dynamics simulations performed with sequence homologues of ADAM 1 show that the species present in lipid bilayers is only consistent with an evolutionarily conserved homotrimeric model for which we provide a backbone structure. These results support a model where ADAM 1 forms homotrimers as a step to create a fusion active intermediate.

Keywords: ADAM 1; homotrimer; fertilin; fusion; infrared dichroism; molecular dynamics; lipid bilayers; {alpha}-helical bundles


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[Abstract] [Full Text] [PDF]


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