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TitleMaturation cleavage of the murine leukemia virus Env precursor separates the transmembrane subunits to prime it for receptor triggering.
Journal, issue, pagesProc Natl Acad Sci U S A, Vol. 109, Issue 20, Page 7735-7740, Year 2012
Publish dateMay 15, 2012
AuthorsRobin Löving / Shang-Rung Wu / Mathilda Sjöberg / Birgitta Lindqvist / Henrik Garoff /
PubMed AbstractThe Env protein of murine leukemia virus matures by two cleavage events. First, cellular furin separates the receptor binding surface (SU) subunit from the fusion-active transmembrane (TM) subunit ...The Env protein of murine leukemia virus matures by two cleavage events. First, cellular furin separates the receptor binding surface (SU) subunit from the fusion-active transmembrane (TM) subunit and then, in the newly assembled particle, the viral protease removes a 16-residue peptide, the R-peptide from the endodomain of the TM. Both cleavage events are required to prime the Env for receptor-triggered activation. Cryoelectron microscopy (cryo-EM) analyses have shown that the mature Env forms an open cage-like structure composed of three SU-TM complexes, where the TM subunits formed separated Env legs. Here we have studied the structure of the R-peptide precursor Env by cryo-EM. TM cleavage in Moloney murine leukemia virus was inhibited by amprenavir, and the Envs were solubilized in Triton X-100 and isolated by sedimentation in a sucrose gradient. We found that the legs of the R-peptide Env were held together by trimeric interactions at the very bottom of the Env. This suggested that the R-peptide ties the TM legs together and that this prevents the activation of the TM for fusion. The model was supported by further cryo-EM studies using an R-peptide Env mutant that was fusion-competent despite an uncleaved R-peptide. The Env legs of this mutant were found to be separated, like in the mature Env. This shows that it is the TM leg separation, normally caused by R-peptide cleavage, that primes the Env for receptor triggering.
External linksProc Natl Acad Sci U S A / PubMed:22547812 / PubMed Central
MethodsEM (single particle)
Resolution21.0 - 22.0 Å
Structure data

EMDB-2065:
Electron cryo-microscopy of R-peptide precursor of Moloney murine leukemia virus Env in its isomerization arrested intermediate state
Method: EM (single particle) / Resolution: 22.0 Å

EMDB-2066:
Electron cryo-microscopy of the L651A mutant R-peptide precursor Env of Moloney murine leukemia virus in its native state
Method: EM (single particle) / Resolution: 22.0 Å

EMDB-2067:
Electron cryo-microscopy of R-peptide precursor of Moloney murine leukemia virus Env in its native form
Method: EM (single particle) / Resolution: 21.0 Å

Source
  • Moloney murine leukemia virus

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