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人巨细胞病毒:病毒US3基因对宿主免疫的调节

Human cytomegalovirus: host immune modulation by the viral US3 gene.

作者信息

Liu Ziqi, Winkler Michael, Biegalke Bonita

机构信息

Program in Molecular and Cellular Biology, Ohio University, 228 Irvine Hall, Athens, OH 45701, USA.

出版信息

Int J Biochem Cell Biol. 2009 Mar;41(3):503-6. doi: 10.1016/j.biocel.2008.10.012. Epub 2008 Oct 18.

Abstract

Human cytomegalovirus (HCMV) is a common infection, opportunistically causing disease in people with immune system deficits. HCMV expresses several proteins that contribute to avoidance of the host immune response. The US3 gene is one of the first immune evasion genes expressed following infection. Expression of the US3 gene is highly regulated, with the gene encoding autoregulatory proteins. The largest of the US3 proteins, a 22 kDa resident endoplasmic reticulum protein, binds to MHC class I heavy chain complexes and components of the peptide loading complex, delaying the maturation of the MHC class I complexes and presentation of viral antigen on the surface of infected cells. A smaller US3 protein, a 17 kDa US3 protein, competes with the 22 kDa for protein interactions, counteracting, in part, the effects of the larger protein. The US3 amino acid sequence is highly conserved among clinical isolates and laboratory strains, suggesting an important role for this gene in natural infections in the human host.

摘要

人巨细胞病毒(HCMV)是一种常见感染,在免疫系统有缺陷的人群中会引发机会性疾病。HCMV表达多种有助于逃避宿主免疫反应的蛋白质。US3基因是感染后最早表达的免疫逃避基因之一。US3基因的表达受到高度调控,该基因编码自身调节蛋白。最大的US3蛋白是一种22 kDa的内质网驻留蛋白,它与MHC I类重链复合物及肽装载复合物的成分结合,延迟MHC I类复合物的成熟以及病毒抗原在受感染细胞表面的呈递。一种较小的US3蛋白,即17 kDa的US3蛋白,与22 kDa的蛋白竞争蛋白质相互作用,部分抵消了较大蛋白的作用。US3氨基酸序列在临床分离株和实验室菌株中高度保守,表明该基因在人类宿主的自然感染中起重要作用。

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