Stapled helical peptides bearing different anchoring residues
A large proportion of protein–protein interactions (PPIs) occur between a short peptide and a
globular protein domain; the peptides involved in surface interactions play important roles …
globular protein domain; the peptides involved in surface interactions play important roles …
Macrocyclization strategies for cyclic peptides and peptidomimetics
C Bechtler, C Lamers - RSC Medicinal Chemistry, 2021 - pubs.rsc.org
Peptides are a growing therapeutic class due to their unique spatial characteristics that can
target traditionally “undruggable” protein–protein interactions and surfaces. Despite their …
target traditionally “undruggable” protein–protein interactions and surfaces. Despite their …
Recent advances of thiol-selective bioconjugation reactions
P Ochtrop, CPR Hackenberger - Current Opinion in Chemical Biology, 2020 - Elsevier
Proteins are the most abundant biomolecules within a cell and are involved in all
biochemical cellular processes, fulfilling specific functions with unmatched precision. This …
biochemical cellular processes, fulfilling specific functions with unmatched precision. This …
Arylation chemistry for bioconjugation
C Zhang, EV Vinogradova… - Angewandte Chemie …, 2019 - Wiley Online Library
Bioconjugation chemistry has been used to prepare modified biomolecules with functions
beyond what nature intended. Central to these techniques is the development of highly …
beyond what nature intended. Central to these techniques is the development of highly …
Cyclic Peptide Screening Methods for Preclinical Drug Discovery: Miniperspective
X Li, TW Craven, PM Levine - Journal of Medicinal Chemistry, 2022 - ACS Publications
Cyclic peptides are among the most diverse architectures for current drug discovery efforts.
Their size, stability, and ease of synthesis provide attractive scaffolds to engage and …
Their size, stability, and ease of synthesis provide attractive scaffolds to engage and …
A strategy to select macrocyclic peptides featuring asymmetric molecular scaffolds as cyclization units by phage display
TR Oppewal, ID Jansen, J Hekelaar… - Journal of the American …, 2022 - ACS Publications
Macrocyclic peptides (MPs) have positioned themselves as a privileged class of compounds
for the discovery of therapeutics and development of chemical probes. Aided by the …
for the discovery of therapeutics and development of chemical probes. Aided by the …
Genetically encoded fragment-based discovery from phage-displayed macrocyclic libraries with genetically encoded unnatural pharmacophores
AI Ekanayake, L Sobze, P Kelich, J Youk… - Journal of the …, 2021 - ACS Publications
Genetically encoded macrocyclic peptide libraries with unnatural pharmacophores are
valuable sources for the discovery of ligands for many targets of interest. Traditionally …
valuable sources for the discovery of ligands for many targets of interest. Traditionally …
Discovery of Thioether-Cyclized Macrocyclic Covalent Inhibitors by mRNA Display
Macrocyclic peptides are promising scaffolds for the covalent ligand discovery. However,
platforms enabling the direct identification of covalent macrocyclic ligands in a high …
platforms enabling the direct identification of covalent macrocyclic ligands in a high …
Chemical modification of proteins–challenges and trends at the start of the 2020s
NH Fischer, MT Oliveira, F Diness - Biomaterials Science, 2023 - pubs.rsc.org
Ribosomally expressed proteins perform multiple, versatile, and specialized tasks
throughout Nature. In modern times, chemically modified proteins, including improved …
throughout Nature. In modern times, chemically modified proteins, including improved …
Palladium oxidative addition complexes for peptide and protein cross-linking
A new method for cysteine–lysine cross-linking in peptides and proteins using palladium
oxidative addition complexes is presented. First, a biarylphosphine-supported palladium …
oxidative addition complexes is presented. First, a biarylphosphine-supported palladium …