Multimodality probes appear of great interest for innovative imaging applications in disease diagnosis. Herein, we present a chemical strategy enabling site-specific doublemodification and cyclization of a peptide probe exploiting native chemical ligation (NCL) and thiol-maleimide addition. The synthetic strategy is straightforward and of general applicability for the development of double-labeled peptide multimodality probes.

A Chemical Strategy for the Preparation of Multimodified Peptide Imaging Probes

De Rosa, Lucia
Co-primo
;
Di Stasi, Rossella;D'Andrea, Luca Domenico
Ultimo
2023

Abstract

Multimodality probes appear of great interest for innovative imaging applications in disease diagnosis. Herein, we present a chemical strategy enabling site-specific doublemodification and cyclization of a peptide probe exploiting native chemical ligation (NCL) and thiol-maleimide addition. The synthetic strategy is straightforward and of general applicability for the development of double-labeled peptide multimodality probes.
2023
Istituto di Scienze e Tecnologie Chimiche "Giulio Natta" - SCITEC
Istituto di Biostrutture e Bioimmagini - IBB - Sede Napoli
Cyclization
Monomers
Organic polymers
Peptides and proteins
Probes
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/463627
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