PH ON-OFF SWITCHING OF ANTIBODY HAPTEN BINDING BY SITE-SPECIFIC CHEMICAL MODIFICATION OF TYROSINE

被引:27
作者
TAWFIK, DS
CHAP, R
ESHHAR, Z
GREEN, BS
机构
[1] HEBREW UNIV JERUSALEM,FAC MED,DEPT PHARMACEUT CHEM,IL-91120 JERUSALEM,ISRAEL
[2] WEIZMANN INST SCI,DEPT CHEM IMMUNOL,IL-76100 REHOVOT,ISRAEL
来源
PROTEIN ENGINEERING | 1994年 / 7卷 / 03期
关键词
ANTIBODY ENGINEERING; BINDING REGULATION; NITROTYROSINE; TETRANITROMETHANE;
D O I
10.1093/protein/7.3.431
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
Tetranitromethane (TNM) chemically mutates the binding sites of antibodies so that the nitrated antibodies exhibit pa-dependent binding near physiological pH. Three monoclonal antibodies were selectively modified, each under different conditions, with the resultant loss of binding activity at pH > 8 which is recovered at pH < 6. Recovery and loss of binding are ascribed to the protonation and deprotonation, respectively, of the hydroxyl group of the resulting 3-nitrotyrosine side chain (pK(a) similar to 7) at the binding site of these antibodies. pH on-off dependency of binding activity, common to all TNM-modified antibodies studied by us so far, may find use in a variety of applications in which controlled modulation under mild conditions is required.
引用
收藏
页码:431 / 434
页数:4
相关论文
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TAWFIK, DS ;
GREEN, BS ;
CHAP, R ;
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ESHHAR, Z .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (02) :373-377