Identification of residues in the putative 5th helical region of human interleukin-6, important for activation of the IL-6 signal transducer, gp130

被引:6
作者
Brakenhoff, JPJ
Bos, HK
Grotzinger, J
RoseJohn, S
Aarden, LA
机构
[1] UNIV AMSTERDAM, EXPT & CLIN IMMUNOL LAB, NL-1066 CX AMSTERDAM, NETHERLANDS
[2] RHEIN WESTFAL TH AACHEN, DEPT BIOCHEM, D-52057 AACHEN, GERMANY
[3] UNIV MAINZ, SECT PATHOPHYSIOL, MED CLIN 1, D-55101 MAINZ, GERMANY
来源
FEBS LETTERS | 1996年 / 395卷 / 2-3期
关键词
interleukin-6; structure-function analysis; gp130;
D O I
10.1016/0014-5793(96)00974-X
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
We have previously shown that L58 in the putative 5th helical region of human interleukin-6 (IL-6) is important for activation of the IL-6 signal transducer gp130 [de Hon et al. (1995) FEBS Lett, 369, 187-191]. To further explore the importance of individual residues in this region for gp130 activation we have now combined Ala substitutions of residues E52, S53, S54, K55, E56, L58 and E60 with other substitutions in IL-6, known to affect gp130 activation (Q160E and T163P). The combination mutant protein with L58A completely lost the capacity to induce the proliferation of XG-1 myeloma cells, and could effectively antagonize wild type IL-6 activity on these cells. Moreover, the data suggest that besides L58, S54 particularly, but also E52, S53, K55 and E56 contribute to gp130 activation.
引用
收藏
页码:235 / 240
页数:6
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