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[载脂蛋白B编辑酶催化多肽样蛋白3G抗病毒机制的研究进展]

[Recent advances in the study of mechanism of APOBEC3G against virus].

作者信息

Zhu Yan-Ping, Jiang Jian-Dong, Peng Zong-Gen

出版信息

Yao Xue Xue Bao. 2014 Jan;49(1):30-6.

Abstract

APOBEC3 is a class of cytidine deaminase, which is considered as a new member of the innate immune system, and APOBEC3G belongs to this family. The research about APOBEC3G is a new direction of innate immune defense mechanism against virus. APOBEC3G has the restrictive activity on many viral replications, which deaminates dC to dU in the viral genome and then induces extensive hypermutation. APOBEC3G can also interrupt viral replication at several phases such as reverse transcription, replication, nucleocapsid and so on by non-deamination mechanisms. However, virus can encode viral proteins to counteract the restriction activity of APOBEC3G. Elucidation of the antagonistic interaction between APOBEC3G and the virus will be contributed to development of new antiviral drugs in the future.

摘要

载脂蛋白B mRNA编辑酶催化多肽样蛋白3(APOBEC3)是一类胞苷脱氨酶,被认为是天然免疫系统的新成员,而载脂蛋白B mRNA编辑酶催化多肽样蛋白3G(APOBEC3G)属于该家族。对APOBEC3G的研究是天然免疫防御病毒机制的一个新方向。APOBEC3G对多种病毒复制具有限制活性,它在病毒基因组中将脱氧胞苷(dC)脱氨为脱氧尿苷(dU),进而诱导广泛的超突变。APOBEC3G还可通过非脱氨机制在逆转录、复制、核衣壳等多个阶段中断病毒复制。然而,病毒可编码病毒蛋白来对抗APOBEC3G的限制活性。阐明APOBEC3G与病毒之间的拮抗相互作用将有助于未来新型抗病毒药物的研发。

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