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Amino acid sequencing methods of the amino terminus of the protein

机译:蛋白质氨基末端的氨基酸测序方法

摘要

PROBLEM TO BE SOLVED: To make determinable an amino acid sequence by chemically/ biochemically cutting protein having a modified amino-terminal, allowing carboxylic acid anhydride or an isocyanate compound to act on the obtained peptide, analyzing the mass of peptide before and after the action of carboxylic acid anhydride or isocyanate compound, and comparing the results to specify peptide.;SOLUTION: A protein having a modified amino-terminal is cut by a chemical/biochemical means, carboxylic acid anhydride represented by (R1CO)2O is made to act on the obtained peptide when the pH is below 5, and an isocyanate compound represented by R2 NCO is acted on the same when pH is below 6. In the formulas, R1 is an alkyl group, R2 is an optionally substituted alkyl group, phenyl group, naphthyl group or pyridyl group. The mass of peptide before and after the action is analyzed, the results are compared to specify peptide derived from an amino-terminal of protein, and the amino acid sequence of a specified peptide is determined. Thereby, N-end amino acid can be modified with high selectivity even in the co-existence of ε-amino group.;COPYRIGHT: (C)2000,JPO
机译:解决的问题:通过化学/生化切割具有修饰的氨基末端的蛋白质,使羧酸酐或异氰酸酯化合物作用于所得肽上,分析该作用前后的肽质量来确定氨基酸序列解决方案:通过化学/生化手段切割具有修饰的氨基末端的蛋白质,使以(R1CO)2O表示的羧酸酐作用于当pH低于5时,得到的肽,当pH低于6时,由R2 NCO代表的异氰酸酯化合物作用于该肽。式中,R1为烷基,R2为任选取代的烷基,苯基,萘基或吡啶基。分析作用前后的肽质量,将结果进行比较以指定衍生自蛋白质氨基末端的特定肽,并确定特定肽的氨基酸序列。由此,即使在ε-氨基的共存下,也可以高选择性地修饰N端氨基酸。版权所有:(C)2000,日本特许厅

著录项

  • 公开/公告号JP4524823B2

    专利类型

  • 公开/公告日2010-08-18

    原文格式PDF

  • 申请/专利权人 住友化学株式会社;

    申请/专利号JP19990331123

  • 发明设计人 柳 和則;三上 寿幸;中澤 宏;

    申请日1999-11-22

  • 分类号G01N27/62;G01N33/68;

  • 国家 JP

  • 入库时间 2022-08-21 19:01:34

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