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核酸酶活性提示的白喉毒素第二条细胞毒性途径。

Second cytotoxic pathway of diphtheria toxin suggested by nuclease activity.

作者信息

Chang M P, Baldwin R L, Bruce C, Wisnieski B J

机构信息

Department of Microbiology, University of California, Los Angeles 90024.

出版信息

Science. 1989 Dec 1;246(4934):1165-8. doi: 10.1126/science.2531465.

Abstract

Diphtheria toxin (DTx) provokes extensive internucleosomal degradation of DNA before cell lysis. The possibility that DNA cleavage stems from direct chromosomal attack by intracellular toxin molecules was tested by in vitro assays for a DTx-associated nuclease activity. DTx incubated with DNA in solution or in a DNA-gel assay showed Ca2+- and Mg2+-stimulated nuclease activity. This activity proved susceptible to inhibition by specific antitoxin and migrated with fragment A of the toxin. Assays in which supercoiled double-stranded DNA was used revealed rapid endonucleolytic attack. Discovery of a DTx-associated nuclease activity lends support to the model that DTx-induced cell lysis is not a simple consequence of protein synthesis inhibition.

摘要

白喉毒素(DTx)在细胞裂解前会引发广泛的DNA核小体间降解。通过体外检测与DTx相关的核酸酶活性,来测试DNA切割是否源于细胞内毒素分子对染色体的直接攻击。在溶液中或DNA凝胶分析中与DNA一起孵育的DTx显示出Ca2+和Mg2+刺激的核酸酶活性。该活性被证明易受特异性抗毒素的抑制,并与毒素的A片段一起迁移。使用超螺旋双链DNA的分析显示了快速的内切核酸酶攻击。与DTx相关的核酸酶活性的发现支持了DTx诱导的细胞裂解不是蛋白质合成抑制的简单结果这一模型。

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