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本文引用的文献

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NCp7: targeting a multitask protein for next-generation anti-HIV drug development part 2. Noncovalent inhibitors and nucleic acid binders.NCp7:针对多任务蛋白的下一代抗 HIV 药物研发(第二部分):非共价抑制剂和核酸结合物。
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NCp7: targeting a multitasking protein for next-generation anti-HIV drug development part 1: covalent inhibitors.NCp7:针对多功能蛋白的下一代抗 HIV 药物研发 第 1 部分:共价抑制剂。
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Gag-protease coevolution analyses define novel structural surfaces in the HIV-1 matrix and capsid involved in resistance to Protease Inhibitors.Gag-protease 共进化分析定义了 HIV-1 基质和衣壳中与蛋白酶抑制剂耐药性相关的新型结构表面。
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Viral reverse transcriptases.病毒逆转录酶
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Targeted binding of nucleocapsid protein transforms the folding landscape of HIV-1 TAR RNA.核衣壳蛋白的靶向结合改变了HIV-1 TAR RNA的折叠格局。
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Reverse Transcription of Retroviruses and LTR Retrotransposons.逆转录病毒和 LTR 反转座子的逆转录。
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Advances in targeting nucleocapsid-nucleic acid interactions in HIV-1 therapy.HIV-1治疗中靶向核衣壳-核酸相互作用的进展。
Virus Res. 2014 Nov 26;193:135-43. doi: 10.1016/j.virusres.2014.07.004. Epub 2014 Jul 12.
8
Selection of fully processed HIV-1 nucleocapsid protein is required for optimal nucleic acid chaperone activity in reverse transcription.逆转录过程中,最佳核酸伴侣活性需要经过完全加工的HIV-1核衣壳蛋白。
Virus Res. 2014 Nov 26;193:52-64. doi: 10.1016/j.virusres.2014.06.004. Epub 2014 Jun 20.
9
Distinct nucleic acid interaction properties of HIV-1 nucleocapsid protein precursor NCp15 explain reduced viral infectivity.HIV-1核衣壳蛋白前体NCp15独特的核酸相互作用特性解释了病毒感染性降低的原因。
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10
Retrovirus-specific differences in matrix and nucleocapsid protein-nucleic acid interactions: implications for genomic RNA packaging.逆转录病毒基质蛋白和核衣壳蛋白-核酸相互作用的特异性差异:对基因组 RNA 包装的影响。
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核衣壳蛋白前体NCp9和NCp15抑制HIV-1逆转录酶对AZT终止引物的ATP介导的挽救作用。

Nucleocapsid Protein Precursors NCp9 and NCp15 Suppress ATP-Mediated Rescue of AZT-Terminated Primers by HIV-1 Reverse Transcriptase.

作者信息

Árquez Moisés A, Martín-Alonso Samara, Gorelick Robert J, Scott Walter A, Acosta-Hoyos Antonio J, Menéndez-Arias Luis

机构信息

Grupo de Investigación en Genética, Laboratorio de Genética y Biología Molecular, Facultad de Ciencias Básicas y Biomédicas, Universidad Simón Bolívar, Barranquilla, Colombia.

Ciencias Biomédicas, Universidad del Valle, Cali, Colombia.

出版信息

Antimicrob Agents Chemother. 2020 Sep 21;64(10). doi: 10.1128/AAC.00958-20.

DOI:10.1128/AAC.00958-20
PMID:32747359
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7508609/
Abstract

In HIV-1, development of resistance to AZT (3'-azido-3'-deoxythymidine) is mediated by the acquisition of thymidine analogue resistance mutations (TAMs) (i.e., M41L, D67N, K70R, L210W, T215F/Y, and K219E/Q) in the viral reverse transcriptase (RT). Clinically relevant combinations of TAMs, such as M41L/T215Y or D67N/K70R/T215F/K219Q, enhance the ATP-mediated excision of AZT monophosphate (AZTMP) from the 3' end of the primer, allowing DNA synthesis to continue. Additionally, during HIV-1 maturation, the Gag polyprotein is cleaved to release a mature nucleocapsid protein (NCp7) and two intermediate precursors (NCp9 and NCp15). NC proteins interact with the viral genome and facilitate the reverse transcription process. Using wild-type and TAM-containing RTs, we showed that both NCp9 and NCp15 inhibited ATP-mediated rescue of AZTMP-terminated primers annealed to RNA templates but not DNA templates, while NCp7 had no effect on rescue activity. RNase H inactivation by introducing the active-site mutation E478Q led to the loss of the inhibitory effect shown by NCp9. NCp15 had a stimulatory effect on the RT's RNase H activity not observed with NCp7 and NCp9. However, analysis of RNase H cleavage patterns revealed that in the presence of NCp9, RNA/DNA complexes containing duplexes of 12 bp had reduced stability in comparison with those obtained in the absence of NC or with NCp7 or NCp15. These effects are expected to have a strong influence on the inhibitory action of NCp9 and NCp15 by affecting the efficiency of RNA-dependent DNA polymerization after unblocking DNA primers terminated with AZTMP and other nucleotide analogues.

摘要

在HIV-1中,对齐多夫定(3'-叠氮-3'-脱氧胸苷,AZT)产生耐药性是由病毒逆转录酶(RT)中获得胸苷类似物耐药性突变(TAMs)(即M41L、D67N、K70R、L210W、T215F/Y和K219E/Q)介导的。临床上相关的TAMs组合,如M41L/T215Y或D67N/K70R/T215F/K219Q,增强了ATP介导的从引物3'末端切除AZT单磷酸(AZTMP)的能力,使DNA合成得以继续。此外,在HIV-1成熟过程中,Gag多蛋白被切割以释放成熟的核衣壳蛋白(NCp7)和两个中间前体(NCp9和NCp15)。NC蛋白与病毒基因组相互作用并促进逆转录过程。使用野生型和含有TAM的RT,我们发现NCp9和NCp15均抑制ATP介导的与RNA模板退火的AZTMP终止引物的拯救,但对DNA模板无此作用,而NCp7对拯救活性无影响。通过引入活性位点突变E478Q使核糖核酸酶H失活,导致NCp9所显示的抑制作用丧失。NCp15对RT的核糖核酸酶H活性有刺激作用,而NCp7和NCp9未观察到这种作用。然而核糖核酸酶H切割模式分析表明,在存在NCp9的情况下,与不存在NC或存在NCp7或NCp15时相比,含有12 bp双链体的RNA/DNA复合物稳定性降低。预期这些效应会通过影响以AZTMP和其他核苷酸类似物终止的DNA引物解封后RNA依赖性DNA聚合的效率,对NCp9和NCp15的抑制作用产生强烈影响。