Studies in solid-phase peptide synthesis: A personal perspective

被引:6
作者
Mitchell, Alexander R. [1 ]
机构
[1] Lawrence Livermore Natl Lab, Energet Mat Ctr, Livermore, CA 94550 USA
关键词
solid-phase peptide synthesis; SPPS; side reactions; amino acid insertions; N-alpha-trifluoroacetylation; N-alpha epsilon-alkylation; coupling efficiency in SPPS; deletion sequences; PAM-resin;
D O I
10.1002/bip.20812
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
By the early 1970s it had became apparent that the solid-phase synthesis of ribonuclease A could not be generalized. Consequently, virtually every aspect of solid-phase peptide synthesis (SPPS) was reexamined and improved during the decade of the 1970s. The sensitive detection and elimination of possible side reactions (amino acid insertion, N-alpha-trifluoroacetylation, N-alpha epsilon-alkylation) were examined. The quantitation of coupling efficiency in SPPS as a function of chain length was studied. A new and improved support for SPPS, the "PAM-resin," was prepared and evaluated. These and many other studies from the Merrifield laboratory and elsewhere increased the general acceptance of SPPS leading to the 1984 Nobel Prize in Chemistry for Bruce Merrifield. (C) 2007 Wiley Periodicals, Inc. Biopolymers (Pept Sci) 90: 215-233, 2008.
引用
收藏
页码:215 / 233
页数:19
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