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Expression systems of human β-defensins: vectors, purification and biological activities

机译:人β-防御素的表达系统:载体,纯化和生物学活性

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摘要

Human beta-defensins are 2–5 kDa, cationic, microbicidal peptides, which represent the first-line host defense against several Gram-negative and Gram-positive bacteria, fungi and viruses. They contain a conserved disulfide-bridge pattern of three pairs of intramolecular cystine bonds. The well-known public health problem related with the growing number of multiresistant bacteria has driven research to look for novel antibiotics, such beta-defensins and a feasible way to produce them. Heterologous expression of beta-defensins could be one way to generate large quantities of beta-defensins for clinical research; however, heterologous expression of beta-defensins has some biochemical problems, such toxicity toward the host cell, peptide degradation by proteolytic cell enzymes, size, folding constrains and low recombinant peptide yields. In this communication, several heterologous systems for producing human beta-defensins are reviewed.
机译:人β-防御素是2–5 kDa的阳离子杀微生物肽,代表一线宿主防御多种革兰氏阴性和革兰氏阳性细菌,真菌和病毒的能力。它们包含三对分子内胱氨酸键的保守的二硫键-桥接模式。与多重耐药菌数量增加有关的众所周知的公共卫生问题已推动研究寻找新型抗生素,例如β-防御素以及生产它们的可行方法。 β-防御素的异源表达可能是产生大量β-防御素用于临床研究的一种方法。然而,β-防御素的异源表达存在一些生化问题,例如对宿主细胞的毒性,蛋白水解细胞酶对肽的降解,大小,折叠限制和重组肽产量低。在本通讯中,综述了几种产生人β-防御素的异源系统。

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