Structure and function of chicken interleukin-1 beta mutants: uncoupling of receptor binding and in vivo biological activity

被引:11
作者
Chen, Wen-Ting [1 ,2 ]
Huang, Wen-Yang [1 ,2 ]
Chen, Ting [1 ,2 ]
Salawu, Emmanuel Oluwatobi [1 ,2 ,3 ]
Wang, Dongli [4 ]
Lee, Yi-Zong [1 ,2 ]
Chang, Yuan-Yu [1 ,2 ]
Yang, Lee-Wei [1 ,2 ,3 ]
Sue, Shih-Che [1 ,2 ]
Wang, Xinquan [4 ]
Yin, Hsien-Sheng [1 ,2 ]
机构
[1] Natl Tsing Hua Univ, Inst Bioinformat & Struct Biol, 101,Sect 2,Kuang Fu Rd, Hsinchu 30013, Taiwan
[2] Natl Tsing Hua Univ, Coll Life Sci, 101,Sect 2,Kuang Fu Rd, Hsinchu 30013, Taiwan
[3] Acad Sinica, Taiwan Int Grad Program, Bioinformat Program, Taipei 115, Taiwan
[4] Tsinghua Univ, Sch Life Sci, Beijing 100084, Peoples R China
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
关键词
CRYSTAL-STRUCTURE; IL-6; PRODUCTION; IL-1-BETA; IDENTIFICATION; INDUCTION; SITE; ACTIVATION; PROTEINS; SEQUENCE; IMMUNITY;
D O I
10.1038/srep27729
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Receptor-binding and subsequent signal-activation of interleukin-1 beta (IL-1 beta) are essential to immune and proinflammatory responses. We mutated 12 residues to identify sites important for biological activity and/or receptor binding. Four of these mutants with mutations in loop 9 (T117A, E118K, E118A, E118R) displayed significantly reduced biological activity. Neither T117A nor E118K mutants substantially affected receptor binding, whereas both mutants lack the IL-1 beta signaling in vitro but can antagonize wild-type (WT) IL-1 beta. Crystal structures of T117A, E118A, and E118K revealed that the secondary structure or surface charge of loop 9 is dramatically altered compared with that of wild-type chicken IL-1 beta. Molecular dynamics simulations of IL-1 beta bound to its receptor (IL-1RI) and receptor accessory protein (IL-1RAcP) revealed that loop 9 lies in a pocket that is formed at the IL-1RI/IL-1RAcP interface. This pocket is also observed in the human ternary structure. The conformations of above mutants in loop 9 may disrupt structural packing and therefore the stability in a chicken IL-1 beta/IL-1RI/IL-1RAcP signaling complex. We identify the hot spots in IL-1 beta that are essential to immune responses and elucidate a mechanism by which IL-1 beta activity can be inhibited. These findings should aid in the development of new therapeutics that neutralize IL-1 activity.
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页数:11
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