Target‐templated Construction of Functional Proteomimetics Using Photo‐foldamer Libraries

Current methods for proteomimetic engineering rely on structure‐based design. Here we describe a design strategy that allows the construction of proteomimetics against challenging targets without a priori characterization of the target surface. Our approach relies on (i) a 100‐membered photoreactive...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Wéber Edit
Ábrányi-Balogh Péter
Nagymihály Bence
Karancsiné Menyhárd Dóra
Péczka Nikolett
Gadanecz Márton
Schlosser Gitta (Vácziné)
Orgován Zoltán
Bogár Ferenc
Bajusz Dávid
Kecskeméti Gábor
Szabó Zoltán
Bartus Éva
Tököli Attila
Tóth Gábor
Szalai Tibor V.
Takács Tamás
de Araujo Elvin
Buday László
Perczel András
Martinek Tamás
Keserű György Miklós
Dokumentumtípus: Cikk
Megjelent: 2025
Sorozat:ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 64 No. 2
Tárgyszavak:
doi:10.1002/anie.202410435

mtmt:35431408
Online Access:http://publicatio.bibl.u-szeged.hu/34825
Leíró adatok
Tartalmi kivonat:Current methods for proteomimetic engineering rely on structure‐based design. Here we describe a design strategy that allows the construction of proteomimetics against challenging targets without a priori characterization of the target surface. Our approach relies on (i) a 100‐membered photoreactive foldamer library, the members of which act as local surface mimetics, and (ii) the subsequent affinity maturation of the primary hits using systems chemistry. Two surface‐oriented proteinogenic side chains drove the interactions between the short helical foldamer fragments and the proteins. Diazirine‐based photo‐crosslinking was applied to sensitively detected and localize binding even to shallow and dynamic patches on representatively difficult targets. Photo‐foldamers identified functionally relevant protein interfaces, allosteric and previously unexplored targetable regions on the surface of STAT3 and an oncogenic K‐Ras variant. Target‐templated dynamic linking of foldamer hits resulted in two orders of magnitude affinity improvement in a single step. The dimeric K‐Ras ligand mimicked protein‐like catalytic functions. The photo‐foldamer approach thus enables the highly efficient mapping of protein‐protein interaction sites and provides a viable starting point for proteomimetic ligand development without a priori structural hypotheses.
Terjedelem/Fizikai jellemzők:14
ISSN:1433-7851