Cleavage site analysis in picornaviral polyproteins: Discovering cellular targets by neural networks

被引:203
作者
Blom, N
Hansen, J
Blaas, D
Brunak, S
机构
[1] TECH UNIV DENMARK, CTR BIOL SEQUENCE ANAL, DEPT CHEM, DK-2800 LYNGBY, DENMARK
[2] UNIV VIENNA, INST BIOCHEM, A-1030 VIENNA, AUSTRIA
关键词
cleavage site prediction; neural networks; picornavirus; proteinase; surface exposure;
D O I
10.1002/pro.5560051107
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
Picornaviral proteinases are responsible for maturation cleavages of the viral polyprotein, but also catalyze the degradation of cellular targets. Using graphical visualization techniques and neural network algorithms, we have investigated the sequence specificity of the two proteinases 2A(pro) and 3C(pro). The cleavage of VP0 (giving rise to VP2 and VP4), which is carried out by a so-far unknown proteinase, was also examined. In combination with a novel surface exposure prediction algorithm, our neural network approach successfully distinguishes known cleavage sites from noncleavage sites and yields a more consistent definition of features common to these sites. The method is able to predict experimentally determined cleavage sites in cellular proteins. We present a list of mammalian and other proteins that are predicted to be possible targets for the viral proteinases. Whether these proteins are indeed cleaved awaits experimental verification. Additionally, we report several errors detected in the protein databases. A computer server for prediction of cleavage sites by picornaviral proteinases is publicly available at the e-mail address NetPicoRNA@cbs.dtu.dk or via WWW at http://www.cbs.dtu.dk/services/NetPicoRNA/.
引用
收藏
页码:2203 / 2216
页数:14
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