4.3 Article

Nef protein of human immunodeficiency virus type 1 binds its own myristoylated N-terminus

Journal

BIOLOGICAL CHEMISTRY
Volume 388, Issue 2, Pages 181-183

Publisher

WALTER DE GRUYTER & CO
DOI: 10.1515/BC.2007.020

Keywords

fluorescence titration; peptide binding; protein conformation

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HIV-1 Nef is a small protein (approx. 25 kDa) that is post-translationally modified by myristoylation. To explain its complex activities, a 'Nef-cycle' is discussed, which postulates different molecular conformations of Nef. Using recombinant full-length non-myristoylated Nef and synthetic peptides, we demonstrate by fluorescence titration experiments that a peptide representing the myristoylated N-terminus of Nef is specifically bound by Nef. A non-myristoylated N-terminal fragment of Nef or a myristoylated control peptide does not bind to Nef. These results are the first direct experimental evidence of the existence of a myristate-binding pocket in Nef, a prerequisite of the postulated 'closed' Nef conformation.

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