2 PARTIAL ANTAGONISTS OF HUMAN INTERLEUKIN-2

被引:0
|
作者
WANG, ZY [1 ]
ZHENG, ZC [1 ]
SUN, LY [1 ]
LIU, XY [1 ]
机构
[1] ACAD SINICA,SHANGHAI INST BIOCHEM,SHANGHAI 200031,PEOPLES R CHINA
关键词
INTERLEUKIN-2 (IL-2); INTERLEUKIN-2 RECEPTOR (IL-2R); SITE-DIRECTED MUTAGENESIS; ANTAGONIST; STRUCTURE FUNCTION;
D O I
暂无
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
Using site-directed mutagenesis method, six human interleukin-2 (IL-2) muteins with markedly reduced bioactivities were obtained, among them two muteins 15Val-IL-2 and 126Asp-IL-2 could decrease the biological effect of wild-type IL-2 in a specific concentration range. In assays of competition inhibition to high-affinity IL-2 receptor (IL-2R), 15Val-IL-2 and 126Asp-IL-2 exhibited significant competitive abilities once again. These results showed that 15Val-IL-2 and 126Asp-IL-2 could partially antagonize the function of wild-type IL-2. Taking the analysis of IL-2 secondary structure and the knowledge of interaction between IL-2 and IL-2R into consideration, it may be concluded that the partial antagonism of 15Val-IL-2 and 126Asp-IL-2 lies in that substitution slightly disturb the tertiary binding microenviroment of IL-2 and IL-2R beta gamma subunits, thus interfering the binding of relevant IL-2 residues with IL-2R beta gamma subunits which yet is insufficient to totally disrupt such binding.
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页码:446 / 451
页数:6
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