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由缺乏细胞识别结构域的修饰型绿脓杆菌外毒素A构建的免疫毒素的活性。

Activity of immunotoxins constructed with modified Pseudomonas exotoxin A lacking the cell recognition domain.

作者信息

Kondo T, FitzGerald D, Chaudhary V K, Adhya S, Pastan I

机构信息

Laboratory of Molecular Biology, National Cancer Institute, Bethesda, Maryland 20892.

出版信息

J Biol Chem. 1988 Jul 5;263(19):9470-5.

PMID:3132465
Abstract

Pseudomonas exotoxin (PE) contains three domains whose functions are cell recognition, membrane translocation, and ADP ribosylation of elongation factor 2. PE40 is a form of PE which is missing the cell recognition domain. To study the properties of PE40, it was expressed in Escherichia coli using a vector which contains a T7 phage promoter, an OmpA signal sequence, and that portion of the PE gene encoding PE40. Upon induction with isopropyl-1-thio-beta-D-galactopyranoside, large amounts of PE40 were secreted, and highly purified PE40 was prepared from the culture medium. PE40 was chemically coupled to different monoclonal antibodies, and protein synthesis inhibition activities of these immunotoxins was assessed on various cell lines. These activities were compared with the activities of the corresponding immunotoxins made with native PE. These data indicate that PE40 may be useful in the construction of certain immunotoxins.

摘要

铜绿假单胞菌外毒素(PE)包含三个结构域,其功能分别是细胞识别、膜转运以及对延伸因子2进行ADP核糖基化。PE40是PE的一种形式,缺失细胞识别结构域。为了研究PE40的特性,使用一种载体在大肠杆菌中表达它,该载体包含T7噬菌体启动子、OmpA信号序列以及编码PE40的PE基因部分。用异丙基-1-硫代-β-D-半乳糖吡喃糖苷诱导后,大量的PE40被分泌出来,并从培养基中制备出高度纯化的PE40。将PE40化学偶联到不同的单克隆抗体上,并在各种细胞系上评估这些免疫毒素的蛋白质合成抑制活性。将这些活性与用天然PE制备的相应免疫毒素的活性进行比较。这些数据表明PE40可能在某些免疫毒素的构建中有用。

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