Kawaoka Y, Webster R G
Department of Virology and Molecular Biology, St. Jude Children's Research Hospital, Memphis, TN 38101.
Proc Natl Acad Sci U S A. 1988 Jan;85(2):324-8. doi: 10.1073/pnas.85.2.324.
Cleavage of the hemagglutinin (HA) in tissue culture systems has been correlated with virulence of avian influenza viruses. To examine the structural requirements for cleavage of the HA, the HA gene from a virulent H5 influenza virus was expressed in mammalian cells (CV-1), and the cleavage site of the HA was explored by using site-specific mutagenesis. The expressed HA protein exhibited normal cleavage, transport to the cell membrane, and ability to adsorb and to fuse erythrocytes at pH 5. Site-specific mutagenesis of the HA directly established that (i) most of the basic amino acids at this site are critical for cleavage activation; (ii) besides the connecting peptide sequence, at least one other structural feature of the HA is required for enzyme recognition; and (iii) the length of the connecting peptide can abrogate the structural feature(s).
在组织培养系统中,血凝素(HA)的裂解与禽流感病毒的毒力相关。为了研究HA裂解的结构要求,将一种强毒株H5流感病毒的HA基因在哺乳动物细胞(CV-1)中表达,并通过定点诱变探索HA的裂解位点。所表达的HA蛋白表现出正常的裂解、转运至细胞膜以及在pH 5时吸附和融合红细胞的能力。HA的定点诱变直接证实:(i)该位点的大多数碱性氨基酸对裂解激活至关重要;(ii)除连接肽序列外,HA的至少一个其他结构特征是酶识别所必需的;(iii)连接肽的长度可消除该结构特征。