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通过与外膜蛋白traT融合,使外源抗原在大肠杆菌表面表达。

Expression of foreign antigens on the surface of Escherichia coli by fusion to the outer membrane protein traT.

作者信息

Chang H J, Sheu S Y, Lo S J

机构信息

Institute of Microbiology and Immunology, School of Life Science, National Yang-Ming University, Taipei, Taiwan, Republic of China.

出版信息

J Biomed Sci. 1999 Jan;6(1):64-70. doi: 10.1007/BF02256425.

Abstract

The traT gene is one of the F factor transfer genes and encodes an outer membrane protein which is involved in interactions between an Escherichia coli and its surroundings. This protein was altered so as to permit the expression of foreign proteins on the outer membrane of E. coli in this study. A 729-bp DNA fragment, including the leader and entire structural gene sequence of traT, was amplified and obtained by PCR. This sequence was then subcloned downstream of the tac promoter of pDR540, resulting in a TraT expression vector, pT2. Here, we report that the expression of TraT protein, fused either with a partial pre-S antigen of hepatitis B virus (60 and 98 amino acids, respectively) or with the snake venom rhodostomin (72 amino acids), was successfully achieved on the outer membrane of E. coli, using the pT2 plasmid. This result was demonstrated using dot blot and immunofluorescence analysis. This finding supports the notion that the pT2 plasmid can be used as an E. coli display system. This system can detect a foreign peptide of about 100 amino acid residues in length on the bacterial surface.

摘要

traT基因是F因子转移基因之一,编码一种外膜蛋白,该蛋白参与大肠杆菌与其周围环境之间的相互作用。在本研究中,对该蛋白进行了改造,以便在大肠杆菌外膜上表达外源蛋白。通过PCR扩增并获得了一个729 bp的DNA片段,其中包括traT的前导序列和完整的结构基因序列。然后将该序列亚克隆到pDR540的tac启动子下游,得到TraT表达载体pT2。在此,我们报告使用pT2质粒在大肠杆菌外膜上成功实现了与乙肝病毒部分前S抗原(分别为60和98个氨基酸)或蛇毒罗豆素(72个氨基酸)融合的TraT蛋白的表达。使用斑点印迹和免疫荧光分析证明了这一结果。这一发现支持了pT2质粒可作为大肠杆菌展示系统的观点。该系统能够在细菌表面检测到长度约为100个氨基酸残基的外源肽。

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