Identification and characterization of Spodoptera frugiperda furin:: A thermostable subtilisin-like endoprotease

被引:21
作者
Cieplik, M [1 ]
Klenk, HD [1 ]
Garten, W [1 ]
机构
[1] Univ Marburg, Inst Virol, D-35037 Marburg, Germany
关键词
baculovirus; cysteine-rich domain; peptidylchloromethyl ketones; Spodoptera frugiperda; thermostability; trans-Golgi network proteinase furin (EC 3.4.21.);
D O I
10.1515/bchm.1998.379.12.1433
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
Spodoptera frugiperda (Sf9) cells are widely employed for high-level expression of heterologous recombinant genes from baculovirus vectors. Using a plasmid library encoding cDNA of Sf9 cells we have identified here the Spodoptera frugiperda analog of the proprotein convertase furin which plays an important role in posttranslational protein processing. Spodoptera frugiperda furin (Sfurin) is closest related to Drosophila melanogaster fu rin with which it shares an extended cysteine-rich domain, whereas mammalian furin shows high homology only in the catalytic domain. Mammalian furin and Sfurin were further compared by expression from baculovirus vectors. Substrate specificity and inhibitor profiles are identical for Sfurin and mammalian furin, whereas calcium-dependence, pH-optimum and thermostability differ. Cleavage of recombinant influenza virus hemagglutinin was significantly enhanced in Sf9 cells after overexpression of Sfurin.
引用
收藏
页码:1433 / 1440
页数:8
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