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新城疫病毒核衣壳蛋白上与其磷蛋白相互作用的区域。

Regions on nucleocapsid protein of Newcastle disease virus that interact with its phosphoprotein.

作者信息

Kho C L, Tan W S, Tey B T, Yusoff K

机构信息

Department of Biochemistry and Microbiology, Faculty of Science and Environmental Studies, Universiti Putra Malaysia, Serdang, Selangor, Malaysia.

出版信息

Arch Virol. 2004 May;149(5):997-1005. doi: 10.1007/s00705-003-0273-8. Epub 2004 Jan 29.

Abstract

The nucleocapsid (NP) and phospho-(P) proteins of paramyxoviruses are involved in transcription and replication of the viral genome. An in vitro protein binding assay was used to investigate the regions on NP protein that interact with the P protein of Newcastle disease virus (NDV). Truncated NP mutants were first immobilised on a solid phase and then interacted with radio-labelled [(35)S]-P protein synthesised in rabbit reticulocyte. The interaction affinity was quantitated by measuring the radioactivity that was retained on the solid phase. Using this approach, a highly interactive region was identified to be resided at the first 25 amino acids of NP N-terminus. The interaction between these two proteins remained strong even with the removal of 114 amino acids from the C-terminal end of NP. However, it is possible that the 49 amino acids at the C-terminal end might have another contact region for P protein, which is not as critical as the N-terminal end. The interaction regions mapped in this study are significantly different from the other two paramyxoviruses: Sendai and measles viruses in which the C-termini of their NP proteins play an important role in binding to the P.

摘要

副粘病毒的核衣壳(NP)蛋白和磷(P)蛋白参与病毒基因组的转录和复制。采用体外蛋白结合试验研究NP蛋白上与新城疫病毒(NDV)P蛋白相互作用的区域。首先将截短的NP突变体固定在固相上,然后与在兔网织红细胞中合成的放射性标记的[(35)S]-P蛋白相互作用。通过测量保留在固相上的放射性来定量相互作用亲和力。使用这种方法,一个高度相互作用的区域被确定位于NP N端的前25个氨基酸处。即使从NP的C末端去除114个氨基酸,这两种蛋白之间的相互作用仍然很强。然而,NP C末端的49个氨基酸可能存在另一个与P蛋白的接触区域,但其重要性不如N末端。本研究中定位的相互作用区域与另外两种副粘病毒——仙台病毒和麻疹病毒显著不同,后两者NP蛋白的C末端在与P蛋白结合中起重要作用。

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