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通过非扩散性相变实现HIV-1核心的成熟。

Maturation of the HIV-1 core by a non-diffusional phase transition.

作者信息

Frank Gabriel A, Narayan Kedar, Bess Julian W, Del Prete Gregory Q, Wu Xiongwu, Moran Amy, Hartnell Lisa M, Earl Lesley A, Lifson Jeffrey D, Subramaniam Sriram

机构信息

Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.

AIDS and Cancer Virus Program, Leidos Biomedical Research, Inc., Frederick National Laboratory, Frederick, Maryland 21702, USA.

出版信息

Nat Commun. 2015 Jan 8;6:5854. doi: 10.1038/ncomms6854.

Abstract

The formation of the HIV-1 core is the final step in the viral maturation pathway, resulting in the formation of infectious virus. Most current models for HIV-1 core formation suggest that, upon proteolytic cleavage from the immature Gag, capsid (CA) dissociates into the viral interior before reforming into the core. Here we present evidence for an alternate view of core formation by taking advantage of our serendipitous observation of large membrane-enclosed structures in HIV-1 supernatants from infected cells. Cryo-electron tomographic studies show that these structures, which contain ordered arrays of what is likely the membrane-associated matrix protein, contain multiple cores that can be captured at different stages of maturation. Our studies suggest that HIV maturation involves a non-diffusional phase transition in which the detaching layer of the cleaved CA lattice is gradually converted into a roll that ultimately forms the surface of the mature conical core.

摘要

HIV-1核心的形成是病毒成熟途径的最后一步,导致传染性病毒的形成。目前大多数关于HIV-1核心形成的模型表明,从未成熟的Gag蛋白经蛋白水解切割后,衣壳(CA)在重新形成核心之前解离进入病毒内部。在这里,我们利用偶然观察到的来自感染细胞的HIV-1上清液中的大型膜封闭结构,提出了一种关于核心形成的不同观点的证据。冷冻电子断层扫描研究表明,这些结构包含可能是膜相关基质蛋白的有序阵列,包含多个可在不同成熟阶段捕获的核心。我们的研究表明,HIV成熟涉及一个非扩散性相变,其中切割后的CA晶格的分离层逐渐转变为一个卷,最终形成成熟锥形核心的表面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0631/4354040/388f4e055b0c/ncomms6854-f1.jpg

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