共 161 条
Restriction of HIV-1 and other retroviruses by TRIM5
被引:99
作者:

Ganser-Pornillos, Barbie K.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Virginia, Dept Mol Physiol & Biol Phys, Charlottesville, VA 22903 USA Univ Virginia, Dept Mol Physiol & Biol Phys, Charlottesville, VA 22903 USA

Pornillos, Owen
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Virginia, Dept Mol Physiol & Biol Phys, Charlottesville, VA 22903 USA Univ Virginia, Dept Mol Physiol & Biol Phys, Charlottesville, VA 22903 USA
机构:
[1] Univ Virginia, Dept Mol Physiol & Biol Phys, Charlottesville, VA 22903 USA
基金:
美国国家卫生研究院;
关键词:
IMMUNODEFICIENCY-VIRUS TYPE-1;
MURINE LEUKEMIA VIRUSES;
AMINO-TERMINAL DOMAIN;
HUMAN TRIM5-ALPHA;
REVERSE TRANSCRIPTION;
CYTOPLASMIC BODIES;
CRYSTAL-STRUCTURE;
PREINTEGRATION COMPLEX;
B30.2(SPRY) DOMAIN;
CAPSID RECOGNITION;
D O I:
10.1038/s41579-019-0225-2
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Mammalian cells express a variety of innate immune proteins - known as restriction factors - which defend against invading retroviruses such as HIV-1. Two members of the tripartite motif protein family - TRIM5 alpha and TRIMCyp - were identified in 2004 as restriction factors that recognize and inactivate the capsid shell that surrounds and protects the incoming retroviral core. Research on these TRIM5 proteins has uncovered a novel mode of non-self recognition that protects against cross-species transmission of retroviruses. Our developing understanding of the mechanism of TRIM5 restriction underscores the concept that core uncoating and reverse transcription of the viral genome are coordinated processes rather than discrete steps of the post-entry pathway of retrovirus replication. In this Review, we provide an overview of the current state of knowledge of the molecular mechanism of TRIM5-mediated restriction, highlight recent advances and discuss implications for the development of capsid-targeted antiviral therapeutics.
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页码:546 / 556
页数:11
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