Počet záznamů: 1
Biomimetic Macrocyclic Inhibitors of Human Cathepsin D: Structure–Activity Relationship and Binding Mode Analysis
- 1.0522693 - ÚOCHB 2021 RIV US eng J - Článek v odborném periodiku
Houštecká, Radka - Hadzima, Martin - Fanfrlík, Jindřich - Brynda, Jiří - Pallová, Lenka - Hánová, Iva - Mertlíková-Kaiserová, Helena - Lepšík, Martin - Horn, Martin - Smrčina, M. - Majer, Pavel - Mareš, Michael
Biomimetic Macrocyclic Inhibitors of Human Cathepsin D: Structure–Activity Relationship and Binding Mode Analysis.
Journal of Medicinal Chemistry. Roč. 63, č. 4 (2020), s. 1576-1596. ISSN 0022-2623. E-ISSN 1520-4804
Grant CEP: GA MŠMT(CZ) EF16_019/0000729; GA ČR GA15-18929S; GA MŠMT LO1302
Institucionální podpora: RVO:61388963
Klíčová slova: inhibitor * macrocycle * protease
Obor OECD: Biochemistry and molecular biology
Impakt faktor: 7.446, rok: 2020
Způsob publikování: Omezený přístup
https://pubs.acs.org/doi/10.1021/acs.jmedchem.9b01351
Human cathepsin D (CatD), a pepsin-family aspartic protease, plays an important role in tumor progression and metastasis. Here, we report the development of biomimetic inhibitors of CatD as novel tools for regulation of this therapeutic target. We designed a macrocyclic scaffold to mimic the spatial conformation of the minimal pseudo-dipeptide binding motif of pepstatin A, a microbial oligopeptide inhibitor, in the CatD active site. A library of more than 30 macrocyclic peptidomimetic inhibitors was employed for scaffold optimization, mapping of subsite interactions, and profiling of inhibitor selectivity. Furthermore, we solved high-resolution crystal structures of three macrocyclic inhibitors with low nanomolar or subnanomolar potency in complex with CatD and determined their binding mode using quantum chemical calculations. The study provides a new structural template and functional profile that can be exploited for design of potential chemotherapeutics that specifically inhibit CatD and related aspartic proteases.
Trvalý link: http://hdl.handle.net/11104/0307144
Počet záznamů: 1