鞭毛蛋白
高变区
抗原性
TLR5型
生物
表位
重组DNA
遗传学
抗原
分子生物学
抗体
基因
先天免疫系统
免疫系统
Toll样受体
作者
Fang Liu,Jingyi Yang,Yan Zhang,Demin Zhou,Yao-Qing Chen,Weiwei Gai,Wei Shi,Qiaoli Li,Po Tien,Huimin Yan
标识
DOI:10.1016/j.bbrc.2010.01.077
摘要
Flagellin contains conserved N/C domains for TLR5 binding to activate innate immunity and a middle hypervariable domain harboring the major antigenic epitopes. However, conflict results existed in the previous studies as to whether the hypervariable domain was involved in the cytokine production and adjuvancy of flagellin. Here we constructed three flagellin variants (designated as FliCΔ190–278, FliCΔ220–320, and FliCΔ180–400) with deletions in the hypervariable domain. Our data demonstrated that all deletion variants lost substantial antigenicity but not mucosal adjuvancy. Surprisingly, the variant with deletion of amino acids 220–320 (FliCΔ220–320) induced higher production of IL-8, MCP-1, and TNF-α, and showed higher mucosal adjuvancy than full-length FliC flagellin. Our data supported the notion that the hypervariable domain was involved in the cytokine production by flagellin and more importantly demonstrated that the hypervariable domain was important for the mucosal adjuvancy of flagellin.
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