Studies on Peptides. XLIV. Synthesis of the Basic Trypsin Inhibitor from Bovine Pancreas (Kunitz and Northrop) by the Fragment Condensation Procedure on Polymer Support
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概要
- 論文の詳細を見る
Five protected peptide subunits which cover the entire 58 amino acid residues of the bovine pancreatic basic trypsin inhibitor, i.e., Z-Arg (NO_2)-Pro-Asp (OBzl)-Phe-Cys (Bzl)-Leu-Glu (OBzl)-Pro-Pro-Tyr-Thr-Gly-OH (I, positions 1-12), Z (OMe)-Pro-Cys (Bzl)-Lys (Z)-Ala-Arg (Tos)-Ile-Ile-Arg (Tos)-Tyr-Phe-Tyr-Asn-Ala-Lys (Z)-Ala-Gly-OH (II, positions 13-28), Z (OMe)-Leu-Cys (Bzl)-Gln-Thr-Phe-Val-Tyr-Gly-Gly-OH (III, positions 29-37), Z (OMe)-Cys (Bzl)-Arg (Tos)-Ala-Lys (Z)-Arg (Tos)-Asn-Asn-Phe-Lys (Z)-Ser-Ala-Glu (OBzl)-Cys (Bzl)-Met-Arg (Tos)-Thr-Cys (Bzl)-Gly-OH (IV, positions 38-56), Z (OMe)-Gly-Ala-OH (V, positions 57-58), were successively assembled on the polymer support by means of dicyclohexylcarbodiimide plus N-hydroxysuccinimide. In each step, the Z (OMe) group was deprotected by trifluoroacetic acid and the unreacted amino component on the resin was masked by acetylation. After deblocking of all protecting groups by HF and subsequent oxidation followed by affinity chromatographic purification, a highly active peptide, specific activity 82%, indistinguishable from the natural bovine pancreatic basic trypsin inhibitor, was isolated.
- 社団法人日本薬学会の論文
- 1974-05-25
著者
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矢島 治明
Faculty of Pharmaceutical Sciences, Kyoto University
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木曾 良明
Faculty of Pharmaceutical Sciences, Kyoto University
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木曾 良明
Faculty Of Pharmaceutical Sciences Kyoto University
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矢島 治明
Faculty Of Pharmaceutical Sciences Kyoto University
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