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酶促肽合成的新进展。

New developments in enzymatic peptide synthesis.

作者信息

Wong C H, Wang K T

机构信息

Department of Chemistry, Scripps Research Institute, La Jolla, California 92037.

出版信息

Experientia. 1991 Dec 1;47(11-12):1123-9. doi: 10.1007/BF01918376.

DOI:10.1007/BF01918376
PMID:1765124
Abstract

This review article describes new enzymatic methods developed for the efficient and irreversible synthesis of peptides based on native and modified proteases, and for the synthesis of polypeptides containing D- and/or unnatural amino acids. Potential opportunities for future developments in the field based on new enzymes, tailor-made catalytic antibodies, and on the technique of in vitro mutagenesis are also described.

摘要

这篇综述文章描述了基于天然和修饰蛋白酶开发的用于高效且不可逆合成肽的新酶法,以及用于合成含D-氨基酸和/或非天然氨基酸的多肽的方法。还描述了基于新酶、定制催化抗体和体外诱变技术在该领域未来发展的潜在机会。

相似文献

1
New developments in enzymatic peptide synthesis.酶促肽合成的新进展。
Experientia. 1991 Dec 1;47(11-12):1123-9. doi: 10.1007/BF01918376.
2
Development of new enzymatic catalysts for peptide synthesis in aqueous and organic solvents.用于在水性和有机溶剂中进行肽合成的新型酶催化剂的开发。
Biomed Biochim Acta. 1991;50(10-11):S9-14.
3
New developments in the synthesis of natural and unnatural amino acids.天然和非天然氨基酸合成的新进展。
Ann N Y Acad Sci. 1992 Nov 30;672:510-27.
4
Serine proteinase-catalyzed incorporation of D-amino into model peptides in acetonitrile with low water content.丝氨酸蛋白酶催化在低含水量乙腈中将D-氨基酸掺入模型肽中。
Biomed Biochim Acta. 1991;50(10-11):S44-9.
5
Dynamic kinetic resolution in the asymmetric synthesis of beta-amino acids by organocatalytic reduction of enamines with trichlorosilane.通过三氯硅烷对烯胺进行有机催化还原实现β-氨基酸不对称合成中的动态动力学拆分
Chemistry. 2008;14(27):8082-5. doi: 10.1002/chem.200801244.
6
[Asymmetric Synthesis of Unnatural Amino Acid-containing Peptides via Direct Asymmetric Reaction of Peptidyl Compounds].通过肽基化合物的直接不对称反应实现含非天然氨基酸肽的不对称合成
Yakugaku Zasshi. 2018;138(11):1371-1379. doi: 10.1248/yakushi.18-00143.
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[Enzymatic synthesis of acyl peptides containing p-nitroanilides of basic amino acids].[含碱性氨基酸对硝基苯胺的酰基肽的酶促合成]
Bioorg Khim. 1991 Aug;17(8):1066-73.
8
Robust asymmetric synthesis of unnatural alkenyl amino acids for conformationally constrained α-helix peptides.用于构象受限α-螺旋肽的非天然烯基氨基酸的稳健不对称合成。
Org Biomol Chem. 2014 Nov 21;12(43):8775-82. doi: 10.1039/c4ob01832j.
9
Substrate specificity and stereospecificity of proteases in hydro-organic cosolvent systems.
Biomed Biochim Acta. 1991;50(10-11):S127-30.
10
Enzymatic manipulation of protecting groups: more than deprotection.
Biomed Biochim Acta. 1991;50(10-11):S19-31.

引用本文的文献

1
An enigmatic peptide ligation reaction: protease-catalyzed oligomerization of a native protein segment in neat aqueous solution.一种神秘的肽连接反应:蛋白酶催化的天然蛋白质片段在纯水溶液中的寡聚化。
Protein Sci. 2000 Apr;9(4):734-41. doi: 10.1110/ps.9.4.734.
2
Tuning the activity of an enzyme for unusual environments: sequential random mutagenesis of subtilisin E for catalysis in dimethylformamide.调整酶在特殊环境中的活性:枯草杆菌蛋白酶E在二甲基甲酰胺中催化作用的连续随机诱变
Proc Natl Acad Sci U S A. 1993 Jun 15;90(12):5618-22. doi: 10.1073/pnas.90.12.5618.
3
Physicochemical properties of alkaline serine proteases in alcohol.

本文引用的文献

1
Enzymatic synthesis in biphasic aqueous-organic systems. I. Chemical equilibrium shift.双相水-有机体系中的酶促合成。I. 化学平衡移动
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Separation of the proteolytic and esterasic activities of trypsin by reversible structural modifications.
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Catalysis of a stereospecific bimolecular amide synthesis by an antibody.抗体催化立体特异性双分子酰胺合成。
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6
A general method for site-specific incorporation of unnatural amino acids into proteins.一种将非天然氨基酸位点特异性掺入蛋白质的通用方法。
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7
Generation of a large combinatorial library of the immunoglobulin repertoire in phage lambda.利用λ噬菌体构建免疫球蛋白全套的大型组合文库。
Science. 1989 Dec 8;246(4935):1275-81. doi: 10.1126/science.2531466.
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Peptide and protein synthesis by segment synthesis-condensation.
Science. 1989 Jan 13;243(4888):187-92. doi: 10.1126/science.2492114.
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Diastereoselective hydrolysis of peptide esters by alkaline protease. Preparation of racemization-free peptides.碱性蛋白酶催化肽酯的非对映选择性水解。无消旋肽的制备。
Int J Pept Protein Res. 1991 Apr;37(4):347-50. doi: 10.1111/j.1399-3011.1991.tb00749.x.
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Synthesis of peptide bonds by proteinases. Addition of organic cosolvents shifts peptide bond equilibria toward synthesis.
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