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登革病毒诱导的细胞毒性因子的纯化及氨基末端序列

Purification and amino-terminal sequence of the dengue virus-induced cytotoxic factor.

作者信息

Khanna M, Chaturvedi U C

机构信息

Postgraduate Department of Microbiology, K.G. Medical College, Lucknow, India.

出版信息

Int J Exp Pathol. 1992 Feb;73(1):43-9.

Abstract

The present study was undertaken to purify the dengue type 2 virus (DV)-induced cytotoxic factor (CF) and analyse its amino-terminal sequence. Spleens collected from DV-infected moribund mice were made into a single cell suspension and cultured for 24 h. The culture supernatant was purified using fast protein liquid chromatography (FPLC) and polyacrylamide gel electrophoresis (PAGE). CF could be purified in a single step by FPLC and native PAGE. The isoelectric point of CF was pH 6.5. Purified CF had a molecular weight of 45 kDa on native-PAGE while on SDS-PAGE it dissociated into two bands of 20 and 25 kDa. Anti-CF-antisera reacted specifically with CF bands separated on native and SDS-PAGE in a Western blot assay. A sequence of 19 amino-acids of the N-terminus of CF was analysed which on comparison with that of other known cytotoxic proteins indicated that CF differs from them. Thus, CF appears to be a unique cytotoxic protein induced by a virus.

摘要

本研究旨在纯化登革2型病毒(DV)诱导的细胞毒性因子(CF)并分析其氨基末端序列。从感染DV的濒死小鼠收集脾脏,制成单细胞悬液并培养24小时。培养上清液用快速蛋白质液相色谱(FPLC)和聚丙烯酰胺凝胶电泳(PAGE)进行纯化。CF可通过FPLC和天然PAGE一步纯化。CF的等电点为pH 6.5。纯化的CF在天然PAGE上的分子量为45 kDa,而在SDS-PAGE上则解离为20 kDa和25 kDa的两条带。在蛋白质免疫印迹分析中,抗CF抗血清与在天然和SDS-PAGE上分离的CF条带特异性反应。分析了CF N末端的19个氨基酸序列,与其他已知细胞毒性蛋白的序列比较表明CF与它们不同。因此,CF似乎是一种由病毒诱导的独特细胞毒性蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ac/2002458/d2823121623c/ijexpath00019-0054-a.jpg

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