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CD164 是淋巴细胞性脉络丛脑膜炎病毒进入的宿主因子。

CD164 is a host factor for lymphocytic choriomeningitis virus entry.

机构信息

Department of Microbiology, Harvard Medical School, Boston, MA 02115.

Program in Virology, Harvard Medical School, Boston, MA 02115.

出版信息

Proc Natl Acad Sci U S A. 2022 Mar 8;119(10):e2119676119. doi: 10.1073/pnas.2119676119. Epub 2022 Mar 2.

Abstract

Lymphocytic choriomeningitis virus (LCMV) is a rodent-borne zoonotic arenavirus that causes congenital abnormalities and can be fatal for transplant recipients. Using a genome-wide loss-of-function screen, we identify host factors required for LCMV entry into cells. We identify the lysosomal mucin CD164, glycosylation factors, the heparan sulfate biosynthesis machinery, and the known receptor alpha-dystroglycan (α-DG). Biochemical analysis revealed that the LCMV glycoprotein binds CD164 at acidic pH and requires a sialylated glycan at residue N104. We demonstrate that LCMV entry proceeds by the virus switching binding from heparan sulfate or α-DG at the plasma membrane to CD164 prior to membrane fusion, thus identifying additional potential targets for therapeutic intervention.

摘要

淋巴细胞性脉络丛脑膜炎病毒(Lymphocytic choriomeningitis virus,LCMV)是一种啮齿动物传播的人畜共患病正黏液病毒,可导致先天性异常,并可能对移植受者致命。使用全基因组功能丧失筛选,我们确定了宿主因子对于 LCMV 进入细胞所必需的。我们确定了溶酶体粘蛋白 CD164、糖基化因子、肝素硫酸生物合成机制以及已知的受体α- 肌营养不良蛋白(α-DG)。生化分析表明,LCMV 糖蛋白在酸性 pH 下与 CD164 结合,并且需要残基 N104 上的唾液酸化聚糖。我们证明,LCMV 进入细胞的过程是病毒在膜融合之前从细胞膜上的肝素硫酸或α-DG 切换到 CD164 进行结合,从而确定了其他潜在的治疗干预靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92a2/8915965/da8d96b3ce6c/pnas.2119676119fig01.jpg

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