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Convenient Approach to Polypeptide Copolymers Derived from Native Proteins

机译:天然蛋白衍生的多肽共聚物的简便方法

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摘要

A convenient approach for the synthesis of narrowly dispersed polypeptide copolymers of defined compositions is presented. The controlled denaturation of the proteins serum albumin and lysozyme followed by an in situ stabilization with polyethylene(oxide) chains yields polypeptide side chain copolymers of precisely defined backbone lengths as well as the presence of secondary structure elements, Supramolecular architectures are formed in solution because of the presence of hydrophobic and hydrophilic amino acids along the polypeptide main chain. Polypeptide copolymers reported herein reveal excellent solubility and stability in aqueous media and no significant cytotoxicity at relevant concentrations, and they can be degraded via proteolysis, which is very attractive for biomedical applications. This "semi-synthetic chemistry" approach is based on a novel and convenient concept for producing synthetic polypeptides from native protein resources, which complements traditional polypeptide synthesis and expression approaches and offers great opportunities for the preparation of diverse polypeptides with unique architectures.
机译:提出了一种合成限定组成的窄分散多肽共聚物的简便方法。蛋白质血清白蛋白和溶菌酶的受控变性,然后用聚乙烯氧化物链原位稳定化,可产生具有精确定义的骨架长度的多肽侧链共聚物,并且存在二级结构元件。由于沿着多肽主链存在疏水性和亲水性氨基酸。本文报道的多肽共聚物显示出在水性介质中的优异溶解性和稳定性,并且在相关浓度下没有明显的细胞毒性,并且它们可以通过蛋白水解降解,这对于生物医学应用是非常有吸引力的。这种“半合成化学”方法基于从天然蛋白质资源生产合成多肽的新颖方便的概念,它补充了传统的多肽合成和表达方法,为制备具有独特结构的多种多肽提供了巨大的机会。

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