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PMID: 12873766 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Role of HIV-1 Gag domains in viral assembly.

Biochimica et biophysica acta ·Vol. 1614 ·No. 1 ·2003-07-11 ·Pages 62-72

Scarlata S, Carter C

Abstract

After entry of the human immunodeficiency virus type 1 (HIV-1) into T cells and the subsequent synthesis of viral products, viral proteins and RNA must somehow find each other in the host cells and assemble on the plasma membrane to form the budding viral particle. In this general review of HIV-1 assembly, we present a brief overview of the HIV life cycle and then discuss assembly of the HIV Gag polyprotein on RNA and membrane substrates from a biochemical perspective. The role of the domains of Gag in targeting to the plasma membrane and the role of the cellular host protein cyclophilin are also reviewed.

MeSH Terms
Amino Acid Sequence Cell Membrane/virology Cyclophilins/metabolism Gene Products, gag/chemistry,metabolism Genome, Viral HIV-1/genetics,growth & development,pathogenicity Humans Models, Biological Models, Molecular Protein Structure, Tertiary Virion/growth & development
Chemicals
Gene Products, gag Cyclophilins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Scarlata Suzanne
Department of Physiology and Biophysics, State University of New York at Stony Brook, Stony Brook, NY 11794-8661, USA. suzanne@dualphy.pnb.sunysb.edu
Carter Carol
Article Info
Journal
Biochimica et biophysica acta
Abbr.
Biochim Biophys Acta
ISSN
0006-3002
Published
2003-07-11
Pages
62-72
Language
English
Region
Netherlands
NLM ID
0217513
Subset
IM
Grants
NIGMS NIH HHS · GM58271 · United States
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