寡肽酶
脯氨酸
化学
生物化学
基质(水族馆)
成纤维细胞
底物特异性
立体化学
酶
氨基酸
生物
体外
生态学
作者
Kalyani Jambunathan,Douglas S. Watson,Aaron N. Endsley,Krishna Kodukula,Amit K. Galande
出处
期刊:FEBS Letters
[Wiley]
日期:2012-06-27
卷期号:586 (16): 2507-2512
被引量:17
标识
DOI:10.1016/j.febslet.2012.06.015
摘要
Post‐proline cleaving peptidases are promising therapeutic targets for neurodegenerative diseases, psychiatric conditions, metabolic disorders, and many cancers. Prolyl oligopeptidase (POP; E.C. 3.4.21.26) and fibroblast activation protein α (FAP; E.C. 3.4.24.B28) are two post‐proline cleaving endopeptidases with very similar substrate specificities. Both enzymes are implicated in numerous human diseases, but their study is impeded by the lack of specific substrate probes. We interrogated a combinatorial library of proteolytic substrates and identified novel and selective substrates of POP and FAP. These new sequences will be useful as probes for fundamental biochemical study, scaffolds for inhibitor design, and triggers for controlled drug delivery.
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