The role of matrix in HIV-1 envelope glycoprotein incorporation

被引:54
|
作者
Tedbury, Philip R. [1 ]
Freed, Eric O. [1 ]
机构
[1] NCI, Virus Cell Interact Sect, HIV Drug Resistance Program, Ctr Canc Res, Frederick, MD 21702 USA
基金
美国国家卫生研究院;
关键词
HIV-1; matrix; envelope; assembly; packaging; VIRUS TYPE-1 MATRIX; GP41 CYTOPLASMIC TAIL; MURINE LEUKEMIA-VIRUS; PLASMA-MEMBRANE; RETROVIRAL VECTOR; ENV INCORPORATION; ASSEMBLY SITES; GAG-PROTEINS; MYOSIN VB; IMMUNODEFICIENCY;
D O I
10.1016/j.tim.2014.04.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Incorporation of the viral envelope (Env) glycoprotein is a critical requirement for the production of infectious HIV-1 particles. It has long been appreciated that the matrix (MA) domain of the Gag polyprotein and the cytoplasmic tail of Env are central players in the process of Env incorporation, but the precise mechanisms have been elusive. Several recent developments have thrown light on the contributions of both proteins, prompting a re-evaluation of the role of MA during Env incorporation. The two domains appear to play distinct but complementary roles, with the cytoplasmic tail of Env responsible for directing Env to the site of assembly and the matrix domain accommodating the cytoplasmic tail of Env in the Gag lattice.
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页码:372 / 378
页数:7
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