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与先驱者隔厅相望。

Across the Hall from Pioneers.

机构信息

HIV Dynamics and Replication Program, National Cancer Institute, Frederick, MD 21702, USA.

出版信息

Viruses. 2021 Mar 16;13(3):491. doi: 10.3390/v13030491.

Abstract

I was fortunate to be associated with the lab of Stephen Oroszlan at the US National Cancer Institute from ~1982 until his conversion to Emeritus status in 1995. His lab made groundbreaking discoveries on retroviral proteins during that time, including many features that could not have been inferred or anticipated from straightforward sequence information. Building on the Oroszlan lab results, my colleagues and I demonstrated that the zinc fingers in nucleocapsid proteins play a crucial role in genomic RNA encapsidation; that the N-terminal myristylation of the Gag proteins of many retroviruses is important for their association with the plasma membrane before particle assembly is completed; and that gammaretroviruses initially synthesize their Env protein as an inactive precursor and then truncate the cytoplasmic tail of the transmembrane protein, activating Env fusogenicity, during virus maturation. We also elucidated several aspects of the mechanism of translational suppression in gene expression in gammaretroviruses; amazingly, this is a fundamentally different mechanism of suppression from that in most other retroviral genera.

摘要

我很幸运,从 1982 年左右到 1995 年他转为名誉教授,一直与美国国立癌症研究所的斯蒂芬·奥罗斯兰(Stephen Oroszlan)实验室合作。在此期间,他的实验室在逆转录病毒蛋白方面取得了开创性的发现,其中包括许多仅凭序列信息无法推断或预见的特征。基于奥罗斯兰实验室的结果,我的同事和我证明了核衣壳蛋白中的锌指在基因组 RNA 包装中起着至关重要的作用;许多逆转录病毒的 Gag 蛋白的 N 端豆蔻酰化对于它们在完成颗粒组装之前与质膜的结合很重要;γ逆转录病毒最初将其 Env 蛋白合成作为无活性的前体,然后在病毒成熟过程中截短跨膜蛋白的细胞质尾巴,激活 Env 的融合活性。我们还阐明了γ逆转录病毒基因表达中翻译抑制的几个方面;令人惊讶的是,这是一种与大多数其他逆转录病毒属根本不同的抑制机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67e9/8002223/666ef3e3d5d6/viruses-13-00491-g001.jpg

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