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逆转录病毒出芽。

Retrovirus budding.

作者信息

Demirov Dimiter G, Freed Eric O

机构信息

Virus-Cell Interaction Section, HIV Drug Resistance Program, National Cancer Institute at Frederick, Bldg. 535/Rm. 124, Frederick, MD 21702-1201, USA.

出版信息

Virus Res. 2004 Dec;106(2):87-102. doi: 10.1016/j.virusres.2004.08.007.

Abstract

The release of retrovirus particles from the infected cell is greatly stimulated by short motifs, known as "late" or "L" domains, present within the Gag precursor protein. Three distinct classes of L domains have been identified; these bear the core sequence: Pro-Thr/Ser-Ala-Pro [P(T/S)AP], Pro-Pro-x-Tyr (PPxY), or Tyr-Pro-x-Leu (YPxL). A number of recent studies have demonstrated that L domains function by interacting with components of the machinery responsible for sorting cellular proteins into the multivesicular body (MVB) pathway. This review traces the history of L domain discovery and characterization, and highlights the relationship between L domain activity, retrovirus release, and the host endosomal sorting machinery.

摘要

被感染细胞中逆转录病毒颗粒的释放受到Gag前体蛋白中存在的短基序(称为“晚期”或“L”结构域)的极大刺激。已鉴定出三种不同类型的L结构域;它们具有核心序列:脯氨酸-苏氨酸/丝氨酸-丙氨酸-脯氨酸[P(T/S)AP]、脯氨酸-脯氨酸-x-酪氨酸(PPxY)或酪氨酸-脯氨酸-x-亮氨酸(YPxL)。最近的一些研究表明,L结构域通过与负责将细胞蛋白分选到多泡体(MVB)途径的机制成分相互作用来发挥功能。本综述追溯了L结构域发现和表征的历史,并强调了L结构域活性、逆转录病毒释放与宿主内体分选机制之间的关系。

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