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Università degli Studi di Milano

SALICYLALDEHYDE-TAGGED PEPTIDES FOR THE REVERSIBLE-COVALENT ENGAGEMENT OF PROTEIN LYSINE RESIDUES

Abstract

dc:description

Covalent drug discovery has recently re-emerged as a powerful approach for targeting clinically-relevant proteins, offering enhanced potency and selectivity through controlled covalent interactions. In particular, reversible covalent (RC) chemistry combines the strength of covalent binding with the tunability of non-covalent interactions, mitigating the risks of permanent off-target reactivity. Within this context, this PhD thesis explores the use of salicylaldehyde (SA) as a reversible electrophilic warhead for peptide-based ligand design. The first part of this thesis focuses on the synthesis of SA-modified amino acids and their incorporation into model peptides. Later on, a more straightforward and versatile approach was devised, consisting in the late-stage peptide functionalization with copper-catalyzed azide- alkyne cycloaddition (CuAAC). This second strategy enabled efficient installation of SA moieties onto pre-assembled peptides specific for two protein targets, namely SHP2 and NEMO. Moreover, using human serum albumin as model target, the CuAAC protocol was instrumental for the design of a new combinatorial approach to SA-tagged small molecules. The final part of the work, carried out at the University of Tokyo, integrates SA-based reversible covalent chemistry into the RaPID (Random nonstandard Peptides Integrated Discovery) platform, paving the way to a novel strategy towards macrocyclic peptide libraries displaying a Lys-engaging electrophile. Overall, this work expands the chemical space of peptide-based RC ligands, providing new synthetic and methodological tools to access selective, tunable covalent binders to target specific proteins or to inhibit clinically-relevant protein-protein interactions.

Degree

thesis:*
Grantor dc:publisher
Università degli Studi di Milano
Year dc:date
2026

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • MASON, MATTIA
Contributors dc:contributor
  • tutor: A. Dal Corso ; PhD coordinator: D. Passarella
  • M. Mason
  • DAL CORSO, ALBERTO
  • PASSARELLA, DANIELE

Subjects

dc:subject × 1

Rights

dc:rights
Statement dc:rights
  • info:eu-repo/semantics/embargoedAccess
  • license:Creative commons
  • license uri:http://creativecommons.org/licenses/by-sa/4.0/
Language dc:language
eng

Identifiers

dc:identifier.*
OAI identifier oai:identifier
oai:air.unimi.it:2434/1205020

Chain of custody

source
Harvested from
Università degli Studi di Milano
Base URL
air.unimi.it/oai/request
Last updated
2026-07-27
Source record
OAI-PMH GetRecord
citation

MASON, MATTIA. SALICYLALDEHYDE-TAGGED PEPTIDES FOR THE REVERSIBLE-COVALENT ENGAGEMENT OF PROTEIN LYSINE RESIDUES. Università degli Studi di Milano, 2026. https://hdl.handle.net/2434/1205020