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2
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本文引用的文献

1
Directed evolution of ligand dependence: small-molecule-activated protein splicing.配体依赖性的定向进化:小分子激活的蛋白质剪接
Proc Natl Acad Sci U S A. 2004 Jul 20;101(29):10505-10. doi: 10.1073/pnas.0402762101. Epub 2004 Jul 9.
2
The Staudinger ligation-a gift to chemical biology.施陶丁格连接反应——给化学生物学的一份礼物。
Angew Chem Int Ed Engl. 2004 Jun 14;43(24):3106-16. doi: 10.1002/anie.200401744.
3
Conjugation of glycopeptide thioesters to expressed protein fragments: semisynthesis of glycosylated interleukin-2.糖肽硫酯与表达的蛋白质片段的缀合:糖基化白细胞介素-2的半合成
Methods Mol Biol. 2004;283:255-66. doi: 10.1385/1-59259-813-7:255.
4
Incorporation of nonnatural amino acids into proteins.将非天然氨基酸掺入蛋白质中。
Annu Rev Biochem. 2004;73:147-76. doi: 10.1146/annurev.biochem.73.012803.092429.
5
Simultaneous triggering of protein activity and fluorescence.蛋白质活性与荧光的同步触发。
J Am Chem Soc. 2004 Jun 16;126(23):7170-1. doi: 10.1021/ja0499142.
6
Developments in peptide and amide synthesis.肽与酰胺合成的进展。
Curr Opin Chem Biol. 2004 Jun;8(3):211-21. doi: 10.1016/j.cbpa.2004.03.002.
7
Toward fully synthetic glycoproteins by ultimately convergent routes: a solution to a long-standing problem.通过最终汇聚途径迈向全合成糖蛋白:解决一个长期存在的问题。
J Am Chem Soc. 2004 Jun 2;126(21):6576-8. doi: 10.1021/ja0491836.
8
The ribosome as an entropy trap.核糖体作为一个熵阱。
Proc Natl Acad Sci U S A. 2004 May 25;101(21):7897-901. doi: 10.1073/pnas.0402488101. Epub 2004 May 12.
9
Semisynthesis of phosphovariants of Smad2 reveals a substrate preference of the activated T beta RI kinase.Smad2磷酸化变体的半合成揭示了活化的TβRI激酶的底物偏好。
Biochemistry. 2004 May 18;43(19):5698-706. doi: 10.1021/bi0498407.
10
A one-pot total synthesis of crambin.一种一步法全合成克拉宾。
Angew Chem Int Ed Engl. 2004 May 3;43(19):2534-8. doi: 10.1002/anie.200353540.

蛋白质的化学合成

Chemical synthesis of proteins.

作者信息

Nilsson Bradley L, Soellner Matthew B, Raines Ronald T

机构信息

Department of Chemistry, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

出版信息

Annu Rev Biophys Biomol Struct. 2005;34:91-118. doi: 10.1146/annurev.biophys.34.040204.144700.

DOI:10.1146/annurev.biophys.34.040204.144700
PMID:15869385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2845543/
Abstract

Proteins have become accessible targets for chemical synthesis. The basic strategy is to use native chemical ligation, Staudinger ligation, or other orthogonal chemical reactions to couple synthetic peptides. The ligation reactions are compatible with a variety of solvents and proceed in solution or on a solid support. Chemical synthesis enables a level of control on protein composition that greatly exceeds that attainable with ribosome-mediated biosynthesis. Accordingly, the chemical synthesis of proteins is providing previously unattainable insight into the structure and function of proteins.

摘要

蛋白质已成为化学合成可及的目标。基本策略是使用天然化学连接、施陶丁格连接或其他正交化学反应来偶联合成肽段。这些连接反应与多种溶剂兼容,可在溶液中或在固体支持物上进行。化学合成能够对蛋白质组成进行控制,其程度大大超过核糖体介导的生物合成所能达到的水平。因此,蛋白质的化学合成正在为蛋白质的结构和功能提供前所未有的深入见解。