Mapping protease substrates by using a biotinylated phage substrate library

被引:34
作者
Scholle, Michael D.
Kriplani, Ushma
Pabon, Amanda
Sishtla, Kamakshi
Glucksman, Marc J.
Kay, Brian K.
机构
[1] Argonne Natl Lab, Biosci Unit, Combinatorial Biol Unit, Argonne, IL 60439 USA
[2] Rosalind Franklin Univ Med & Sci, Chicago Med Sch, Dept Biochem & Mol Biol, Abbott Pk, IL 60064 USA
[3] Rosalind Franklin Univ Med & Sci, Chicago Med Sch, Midw Proteome Ctr, Abbott Pk, IL 60064 USA
关键词
combinatorial libraries; peptides; phage display; protease substrates; proteins;
D O I
10.1002/cbic.200500427
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
We describe a bacteriophage M13 substrate library encoding the AviTag (BirA substrate) and combinatorial heptamer peptides displayed at the N terminus of the mature form of capsid protein III. Phages are biotinylated efficiently (>= 50 %) when grown in E. coli cells coexpressing BirA, and such viral particles can be immobilized on a streptavidin-coated support and released by protease cleavage within the combinotorial peptide. We have used this library to map the specificity of human Factor Xa and a neuropeptidase, neurolysin (EC3.4.24.16). Validation by analysis of isolated peptide substrates has revealed that neurolysin recognizes the motif hydrophobic-X-Pro-Arg-hydrophobic, where Arg-hydrophobic is the scissile bond.
引用
收藏
页码:834 / 838
页数:5
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