Selective inhibition of fibroblast activation protein protease based on dipeptide substrate specificity
Selective inhibition of fibroblast activation protein protease based on dipeptide substrate specificity
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DOI:
10.1074/jbc.m511112200
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发表时间:
2006-03-17
影响因子:
4.8
通讯作者:
Wolf, BB
中科院分区:
文献类型:
--
作者:
Edosada, CY;Quan, C;Wolf, BB
Fibroblast activation protein (FAP) is a transmembrane serine peptidase that belongs to the prolyl peptidase family. FAP has been implicated in cancer; however, its specific role remains elusive because inhibitors that distinguish FAP from other prolyl peptidases like dipeptidyl peptidase-4 (DPP-4) have not been developed. To identify peptide motifs for FAP-selective inhibitor design, we used P-2-Pro(1) and acetyl (Ac)-P-2-Pro(1) dipeptide substrate libraries, where P-2 was varied and substrate hydrolysis occurs between Pro(1) and a fluorescent leaving group. With the P-2-Pro(1) library, FAP preferred Ile, Pro, or Arg at the P-2 residue; however, DPP-4 showed broad reactivity against this library, precluding selectivity. By contrast, with the Ac-P-2-Pro(1) library, FAP cleaved only Ac-Gly-Pro, whereas DPP-4 showed little reactivity with all substrates. FAP also cleaved formyl-, benzyloxycarbonyl-, biotinyl-, and peptidyl-Gly-Pro substrates, which DPP-4 cleaved poorly, suggesting an N-acyl-Gly- Pro motif for inhibitor design. Therefore, we synthesized and tested the compound Ac-Gly-prolineboronic acid, which inhibited FAP with a K-i of 23 +/- 3 nM. This was similar to 9- to similar to 5400-fold lower than the Ki values for other prolyl peptidases, including DPP-4, DPP-7, DPP-8, DPP-9, prolyl oligopeptidase, and acylpeptide hydrolase. These results identify Ac-Gly-BoroPro as a FAP-selective inhibitor and suggest that N-acyl-Gly- Pro-based inhibitors will allow testing of FAP as a therapeutic target.