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靶向类胰蛋白酶丝氨酸蛋白酶的新型抑制剂及基于活性的探针

Novel Inhibitors and Activity-Based Probes Targeting Trypsin-Like Serine Proteases.

作者信息

Ferguson Timothy E G, Reihill James A, Martin S Lorraine, Walker Brian

机构信息

Biomolecular Sciences Research Group, School of Pharmacy, Queen's University Belfast, Belfast, United Kingdom.

出版信息

Front Chem. 2022 Apr 21;10:782608. doi: 10.3389/fchem.2022.782608. eCollection 2022.

DOI:10.3389/fchem.2022.782608
PMID:35529696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9068901/
Abstract

The trypsin-like proteases (TLPs) play widespread and diverse roles, in a host of physiological and pathological processes including clot dissolution, extracellular matrix remodelling, infection, angiogenesis, wound healing and tumour invasion/metastasis. Moreover, these enzymes are involved in the disruption of normal lung function in a range of respiratory diseases including allergic asthma where several allergenic proteases have been identified. Here, we report the synthesis of a series of peptide derivatives containing an -alkyl glycine analogue of arginine, bearing differing electrophilic leaving groups (carbamate and triazole urea), and demonstrate their function as potent, irreversible inhibitors of trypsin and TLPs, to include activities from cockroach extract. As such, these inhibitors are suitable for use as activity probes (APs) in activity-based profiling (ABP) applications.

摘要

类胰蛋白酶(TLPs)在许多生理和病理过程中发挥着广泛而多样的作用,包括血栓溶解、细胞外基质重塑、感染、血管生成、伤口愈合以及肿瘤侵袭/转移。此外,这些酶还参与了一系列呼吸系统疾病中正常肺功能的破坏,包括过敏性哮喘,其中已鉴定出几种变应原性蛋白酶。在此,我们报道了一系列含有精氨酸的α-烷基甘氨酸类似物的肽衍生物的合成,这些衍生物带有不同的亲电离去基团(氨基甲酸酯和三唑脲),并证明它们作为胰蛋白酶和TLPs的强效不可逆抑制剂的功能,包括对蟑螂提取物活性的抑制。因此,这些抑制剂适用于基于活性的分析(ABP)应用中的活性探针(APs)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/441e/9068901/a6fe276a6226/fchem-10-782608-g013.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/441e/9068901/a6fe276a6226/fchem-10-782608-g013.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/441e/9068901/965f22f26b59/fchem-10-782608-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/441e/9068901/c13642c44736/fchem-10-782608-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/441e/9068901/d125781c1277/fchem-10-782608-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/441e/9068901/3935f19af6e4/fchem-10-782608-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/441e/9068901/a931aa08e28e/fchem-10-782608-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/441e/9068901/37a192a88df3/fchem-10-782608-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/441e/9068901/2cac791b0063/fchem-10-782608-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/441e/9068901/8ddb65028aa8/fchem-10-782608-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/441e/9068901/c9a6d24995e3/fchem-10-782608-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/441e/9068901/6127c3f72108/fchem-10-782608-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/441e/9068901/afe6ff432846/fchem-10-782608-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/441e/9068901/a6fe276a6226/fchem-10-782608-g013.jpg

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