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The development of a high-affinity conformation-sensitive antibody mimetic using a biocompatible copolymer carrier (iBody)

K. Blažková, J. Beranová, M. Hradilek, L. Kostka, V. Šubr, T. Etrych, P. Šácha, J. Konvalinka

. 2021 ; 297 (5) : 101342. [pub] 20211025

Jazyk angličtina Země Spojené státy americké

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc22003316

Peptide display methods are a powerful tool for discovering new ligands of pharmacologically relevant targets. However, the selected ligands often suffer from low affinity. Using phage display, we identified a new bicyclic peptide binder of prostate-specific membrane antigen (PSMA), a metalloprotease frequently overexpressed in prostate cancer. We show that linking multiple copies of a selected low-affinity peptide to a biocompatible water-soluble N-(2-hydroxypropyl)methacrylamide copolymer carrier (iBody) improved binding of the conjugate by several orders of magnitude. Furthermore, using ELISA, enzyme kinetics, confocal microscopy, and other approaches, we demonstrate that the resulting iBody can distinguish between different conformations of the target protein. The possibility to develop stable, fully synthetic, conformation-selective antibody mimetics has potential applications for molecular recognition, diagnosis and treatment of many pathologies. This strategy could significantly contribute to more effective drug discovery and design.

Citace poskytuje Crossref.org

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$a Peptide display methods are a powerful tool for discovering new ligands of pharmacologically relevant targets. However, the selected ligands often suffer from low affinity. Using phage display, we identified a new bicyclic peptide binder of prostate-specific membrane antigen (PSMA), a metalloprotease frequently overexpressed in prostate cancer. We show that linking multiple copies of a selected low-affinity peptide to a biocompatible water-soluble N-(2-hydroxypropyl)methacrylamide copolymer carrier (iBody) improved binding of the conjugate by several orders of magnitude. Furthermore, using ELISA, enzyme kinetics, confocal microscopy, and other approaches, we demonstrate that the resulting iBody can distinguish between different conformations of the target protein. The possibility to develop stable, fully synthetic, conformation-selective antibody mimetics has potential applications for molecular recognition, diagnosis and treatment of many pathologies. This strategy could significantly contribute to more effective drug discovery and design.
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$a Beranová, Jana $u Institute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czech Republic; First Medical Faculty, Charles University, Prague, Czech Republic
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$a Hradilek, Martin $u Institute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czech Republic
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$a Kostka, Libor $u Institute of Macromolecular Chemistry, Czech Academy of Sciences, Prague, Czech Republic
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$a Šubr, Vladimír $u Institute of Macromolecular Chemistry, Czech Academy of Sciences, Prague, Czech Republic
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$a Etrych, Tomáš $u Institute of Macromolecular Chemistry, Czech Academy of Sciences, Prague, Czech Republic
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$a Šácha, Pavel $u Institute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czech Republic. Electronic address: pavelsacha@gmail.com
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$a Konvalinka, Jan $u Institute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czech Republic; Department of Cell and Developmental Biology, Faculty of Science, Charles University, Prague, Czech Republic. Electronic address: jan.konvalinka@uochb.cas.cz
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