ALIX is recruited temporarily into HIV-1 budding sites at the end of gag assembly.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 24834918.
- Also identified by DOI 10.1371/journal.pone.0096950 and PMC identifier 4023924.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Polymerization of Gag on the inner leaflet of the plasma membrane drives the assembly of Human Immunodeficiency Virus 1 (HIV-1). Gag recruits components of the endosomal sorting complexes required for transport (ESCRT) to facilitate membrane fission and virion release. ESCRT assembly is initiated by recruitment of ALIX and TSG101/ESCRT-I, which bind directly to the viral Gag protein and then recruit the downstream ESCRT-III and VPS4 factors to complete the budding process. In contrast to previous models, we show that ALIX is recruited transiently at the end of Gag assembly, and that most ALIX molecules are recycled into the cytosol as the virus buds, although a subset remains within the virion. Our experiments imply that ALIX is recruited to the neck of the assembling virion and is mostly recycled after virion release.
Medical subject headings
- Calcium-Binding Proteins
- Cell Cycle Proteins
- DNA-Binding Proteins
- Endosomal Sorting Complexes Required for Transport
- HIV-1
- Transcription Factors
- Virus Assembly
- gag Gene Products, Human Immunodeficiency Virus