Mizel Steven B, West A Phillip, Hantgan Roy R
Department of Microbiology, Wake Forest University School of Medicine, Winston-Salem, North Carolina 27157, USA.
J Biol Chem. 2003 Jun 27;278(26):23624-9. doi: 10.1074/jbc.M303481200. Epub 2003 Apr 23.
Flagellins from Gram-negative bacteria activate inflammatory cells by a toll-like receptor 5 (TLR5)-dependent signaling pathway. We have examined the interaction between flagellin and TLR5 using an in vitro binding assay. Purified recombinant His-tagged flagellin from Salmonella enteritidis bound to TLR5 in detergent lysates from COS-1 cells transiently transfected with a human TLR5 expression plasmid. Flagellins from Salmonella typhimurium and Escherichia coli also bound to TLR5. The specificity of this interaction was demonstrated by its concentration dependence and lack of TLR5 binding to a biologically inactive form of flagellin or to a His-tagged non-flagellar protein. Flagellin bound to the extracellular domain of TLR5 expressed on the surface of COS-1 cells and to a soluble, monomeric form of the extracellular domain (amino acids 1-636). Although a TLR5 extracellular domain containing amino acids 1-407 retained flagellin binding activity, binding was not evident with a TLR5 peptide encoding residues 1-386. Conversely, a peptide containing amino acid residues 386-636 retained flagellin binding. Thus it is likely that amino acids 386-407 is a binding site for flagellin. This sequence contains a putative leucine-rich repeat. These results support the conclusion that flagellin signaling via TLR5 involves a direct interaction between flagellin and a leucine-rich region in TLR5. We also show that the NH2-terminal 358 amino acids of TLR5 play an important role in its signaling activity. Our results provide, for the first time, a molecular basis for the agonist specificity of a TLR.
革兰氏阴性菌的鞭毛蛋白通过Toll样受体5(TLR5)依赖性信号通路激活炎性细胞。我们使用体外结合试验研究了鞭毛蛋白与TLR5之间的相互作用。从肠炎沙门氏菌纯化的重组His标签鞭毛蛋白与用人类TLR5表达质粒瞬时转染的COS-1细胞的去污剂裂解物中的TLR5结合。鼠伤寒沙门氏菌和大肠杆菌的鞭毛蛋白也与TLR5结合。这种相互作用的特异性通过其浓度依赖性以及TLR5不与生物无活性形式的鞭毛蛋白或His标签非鞭毛蛋白结合来证明。鞭毛蛋白与COS-1细胞表面表达的TLR5细胞外结构域以及细胞外结构域的可溶性单体形式(氨基酸1-636)结合。虽然包含氨基酸1-407的TLR5细胞外结构域保留了鞭毛蛋白结合活性,但编码残基1-386的TLR5肽未显示明显结合。相反,包含氨基酸残基386-636的肽保留了鞭毛蛋白结合。因此,氨基酸386-407可能是鞭毛蛋白的结合位点。该序列包含一个假定的富含亮氨酸重复序列。这些结果支持以下结论:通过TLR5的鞭毛蛋白信号传导涉及鞭毛蛋白与TLR5中富含亮氨酸区域之间的直接相互作用。我们还表明,TLR5的NH2末端358个氨基酸在其信号传导活性中起重要作用。我们的结果首次为TLR的激动剂特异性提供了分子基础。