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Alix 作为衔接蛋白,允许人类副流感病毒 1 与宿主细胞 ESCRT 系统相互作用。

Alix serves as an adaptor that allows human parainfluenza virus type 1 to interact with the host cell ESCRT system.

机构信息

Laboratory of Infectious Diseases, RNA Viruses Section, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, United States of America.

出版信息

PLoS One. 2013;8(3):e59462. doi: 10.1371/journal.pone.0059462. Epub 2013 Mar 19.

Abstract

The cellular ESCRT (endosomal sorting complex required for transport) system functions in cargo-sorting, in the formation of intraluminal vesicles that comprise multivesicular bodies (MVB), and in cytokinesis, and this system can be hijacked by a number of enveloped viruses to promote budding. The respiratory pathogen human parainfluenza virus type I (HPIV1) encodes a nested set of accessory C proteins that play important roles in down-regulating viral transcription and replication, in suppressing the type I interferon (IFN) response, and in suppressing apoptosis. Deletion or mutation of the C proteins attenuates HPIV1 in vivo, and such mutants are being evaluated preclinically and clinically as vaccines. We show here that the C proteins interact and co-localize with the cellular protein Alix, which is a member of the class E vacuolar protein sorting (Vps) proteins that assemble at endosomal membranes into ESCRT complexes. The HPIV1 C proteins interact with the Bro1 domain of Alix at a site that is also required for the interaction between Alix and Chmp4b, a subunit of ESCRT-III. The C proteins are ubiquitinated and subjected to proteasome-mediated degradation, but the interaction with AlixBro1 protects the C proteins from degradation. Neither over-expression nor knock-down of Alix expression had an effect on HPIV1 replication, although this might be due to the large redundancy of Alix-like proteins. In contrast, knocking down the expression of Chmp4 led to an approximately 100-fold reduction in viral titer during infection with wild-type (WT) HPIV1. This level of reduction was similar to that observed for the viral mutant, P(C-) HPIV1, in which expression of the C proteins were knocked out. Chmp4 is capable of out-competing the HPIV1 C proteins for binding Alix. Together, this suggests a possible model in which Chmp4, through Alix, recruits the C proteins to a common site on intracellular membranes and facilitates budding.

摘要

细胞的 ESCRT(必需的内体分选复合物用于运输)系统在货物分拣、形成包含多泡体(MVB)的腔内小泡以及细胞分裂中起作用,该系统可被多种包膜病毒劫持以促进出芽。呼吸道病原体人副流感病毒 1 型(HPIV1)编码一组嵌套的辅助 C 蛋白,这些蛋白在下调病毒转录和复制、抑制 I 型干扰素(IFN)反应和抑制细胞凋亡方面发挥重要作用。C 蛋白的缺失或突变会使 HPIV1 在体内减毒,并且这些突变体正在进行临床前和临床评估作为疫苗。我们在这里表明,C 蛋白与细胞蛋白 Alix 相互作用并共定位,Alix 是 E 类液泡蛋白分选(Vps)蛋白的成员,该蛋白在内体膜上组装成 ESCRT 复合物。HPIV1 C 蛋白与 Alix 的 Bro1 结构域相互作用,该位点也是 Alix 与 ESCRT-III 的 Chmp4b 亚基相互作用所必需的。C 蛋白被泛素化并被蛋白酶体介导的降解,但与 AlixBro1 的相互作用保护 C 蛋白免受降解。Alix 表达的过表达或敲低均未对 HPIV1 复制产生影响,尽管这可能是由于 Alix 样蛋白的大量冗余所致。相比之下,敲低 Chmp4 的表达会导致野生型(WT)HPIV1 感染时病毒滴度降低约 100 倍。这种降低水平与 C 蛋白表达被敲除的病毒突变体 P(C-) HPIV1 观察到的水平相似。Chmp4 能够与 HPIV1 C 蛋白竞争结合 Alix。综上所述,这表明了一种可能的模型,即 Chmp4 通过 Alix 将 C 蛋白募集到细胞内膜上的共同部位,并促进出芽。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e957/3602193/267827f403f5/pone.0059462.g001.jpg

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