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用于多肽合成的自组装模板。

Self-assembled templates for polypeptide synthesis.

作者信息

Ryadnov Maxim G, Woolfson Derek N

机构信息

School of Chemistry, University of Bristol, Cantock's Close, Bristol BS8 1TS, UK.

出版信息

J Am Chem Soc. 2007 Nov 14;129(45):14074-81. doi: 10.1021/ja072960s. Epub 2007 Oct 20.

Abstract

The chemical synthesis of polypeptide chains >50 amino acids with prescribed sequences is challenging. In one approach, native chemical ligation (NCL), short, unprotected peptides are connected through peptide bonds to render proteins in water. Here we combine chemical ligation with peptide self-assembly to deliver extremely long polypeptide chains with stipulated, repeated sequences. We use a self-assembling fiber (SAF) system to form structures tens of micrometers long. In these assemblies, tens of thousands of peptides align with their N- and C-termini abutting. This arrangement facilitates chemical ligation without the usual requirement for a catalytic cysteine residue at the reactive N-terminus. We introduced peptides with C-terminal thioester moieties into the SAFs. Subsequent ligation and disassembly of the noncovalent components produced extended chains > or =10 microm long and estimated at > or =3 MDa in mass. These extremely long molecules were characterized by a combination of biophysical, hydrodynamic, and microscopic measurements.

摘要

化学合成具有特定序列且氨基酸数量超过50个的多肽链具有挑战性。在一种方法中,即天然化学连接(NCL),短的、未受保护的肽通过肽键连接,从而在水中生成蛋白质。在此,我们将化学连接与肽自组装相结合,以递送具有规定重复序列的极长多肽链。我们使用自组装纤维(SAF)系统来形成长达数十微米的结构。在这些组装体中,数以万计的肽以其N端和C端相邻的方式排列。这种排列方式有助于化学连接,而无需在反应性N端通常所需的催化性半胱氨酸残基。我们将带有C端硫酯部分的肽引入到SAF中。随后对非共价成分进行连接和拆解,得到了长度大于或等于10微米、质量估计大于或等于3兆道尔顿的延伸链。这些极长的分子通过生物物理、流体动力学和显微镜测量相结合的方法进行了表征。

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