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用于监测肉毒杆菌神经毒素B切割作用的突触小泡蛋白片段表达系统的构建。

Production of an expression system for a synaptobrevin fragment to monitor cleavage by botulinum neurotoxin B.

作者信息

Nowakowski J L, Courtney B C, Bing Q A, Adler M

机构信息

Pharmacology Division, U. S. Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, Maryland 21010-5425, USA.

出版信息

J Protein Chem. 1998 Jul;17(5):453-62. doi: 10.1023/a:1022570518330.

Abstract

Recombinant DNA techniques were used to develop an expression system for a 51-amino acid peptide fragment that encompasses residues 44-94 of human synaptobrevin 2. This protein is associated with secretory vesicles of nerve terminals and is a substrate for four of the seven serotypes of botulinum neurotoxin (BoNT). The DNA for the recombinant peptide was amplified by the polymerase chain reaction and cloned into the pTrxFus vector. The resulting synaptobrevin peptide was expressed as a thioredoxin fusion protein in E. coli and released into the medium by osmotic lysis. The 18.7-kDa thioredoxin-synaptobrevin protein, designated as TSB-51, is intended for use in a cell-free assay to test potential inhibitors of BoNT/B-mediated proteolysis of synaptobrevin with the ultimate aim of developing clinically effective therapeutic agents to counteract botulism. Incubation of TSB-51 with the purified light chain of BoNT/B resulted in proteolysis which was evident within 30 min and increased with time until completion (approximately 4 hr). Cleavage of TSB-51 appeared to be at the appropriate BoNT/B cleavage site as indicated by a reduced intensity of the 18.7-kDa band and the appearance of a band at 16.4 kDa on Tris-tricene polyacrylamide gradient gels. The concentration of free Zn2+ had a significant effect on the cleavage rate; low Zn2+ concentrations stimulated substrate cleavage, whereas high concentrations were inhibitory. Cleavage was not significantly depressed by the naturally occurring metalloprotease inhibitor phosphoramidon when tested at concentrations up to 5 mM. TSB-51 appears to be a useful substrate for studying BoNT/B and is expected to aid in the discovery of effective BoNT inhibitors.

摘要

利用重组DNA技术开发了一种表达系统,用于表达一种51个氨基酸的肽片段,该片段包含人突触小泡蛋白2的44 - 94位残基。这种蛋白质与神经末梢的分泌囊泡相关,并且是七种肉毒杆菌神经毒素(BoNT)血清型中四种的作用底物。通过聚合酶链反应扩增重组肽的DNA,并将其克隆到pTrxFus载体中。所得的突触小泡蛋白肽在大肠杆菌中作为硫氧还蛋白融合蛋白表达,并通过渗透裂解释放到培养基中。18.7 kDa的硫氧还蛋白 - 突触小泡蛋白,命名为TSB - 51,旨在用于无细胞测定,以测试BoNT/B介导的突触小泡蛋白蛋白水解的潜在抑制剂,最终目标是开发临床上有效的治疗药物来对抗肉毒中毒。TSB - 51与纯化的BoNT/B轻链孵育导致蛋白水解,在30分钟内明显可见,并随时间增加直至完成(约4小时)。如Tris - tricene聚丙烯酰胺梯度凝胶上18.7 kDa条带强度降低以及16.4 kDa条带出现所示,TSB - 51的切割似乎发生在合适 的BoNT/B切割位点。游离Zn2+的浓度对切割速率有显著影响;低Zn2+浓度刺激底物切割,而高浓度则具有抑制作用。当在高达5 mM的浓度下测试时,天然存在的金属蛋白酶抑制剂磷酰胺素对切割没有明显抑制作用。TSB - 51似乎是研究BoNT/B的有用底物,预计有助于发现有效的BoNT抑制剂。

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