New developments in RiPP discovery, enzymology and engineering

M Montalbán-López, TA Scott, S Ramesh… - Natural product …, 2021 - pubs.rsc.org
Covering: up to June 2020 Ribosomally-synthesized and post-translationally modified
peptides (RiPPs) are a large group of natural products. A community-driven review in 2013 …

Diversification of phage-displayed peptide libraries with noncanonical amino acid mutagenesis and chemical modification

JT Hampton, WR Liu - Chemical reviews, 2024 - ACS Publications
Sitting on the interface between biologics and small molecules, peptides represent an
emerging class of therapeutics. Numerous techniques have been developed in the past 30 …

Methods for generating and screening libraries of genetically encoded cyclic peptides in drug discovery

C Sohrabi, A Foster, A Tavassoli - Nature Reviews Chemistry, 2020 - nature.com
Drug discovery has traditionally focused on using libraries of small molecules to identify
therapeutic drugs, but new modalities, especially libraries of genetically encoded cyclic …

Peptide therapeutics: targeting the undruggable space

N Tsomaia - European journal of medicinal chemistry, 2015 - Elsevier
Rapid advancements in genomics have brought a better understanding of molecular
mechanisms for various pathologies and identified a number of highly attractive target …

Therapeutics targeting the fibrinolytic system

H Lin, L Xu, S Yu, W Hong, M Huang… - Experimental & molecular …, 2020 - nature.com
The function of the fibrinolytic system was first identified to dissolve fibrin to maintain
vascular patency. Connections between the fibrinolytic system and many other physiological …

Phage selection of cyclic peptides for application in research and drug development

K Deyle, XD Kong, C Heinis - Accounts of chemical research, 2017 - ACS Publications
Conspectus Cyclic peptides can bind to protein targets with high affinities and selectivities,
which makes them an attractive modality for the development of research reagents and …

A Cysteine‐Directed Proximity‐Driven Crosslinking Method for Native Peptide Bicyclization

FJ Chen, N Pinnette, F Yang, J Gao - Angewandte Chemie, 2023 - Wiley Online Library
Efficient and site‐specific modification of native peptides and proteins is desirable for
synthesizing antibody‐drug conjugates as well as for constructing chemically modified …

Identification of highly selective covalent inhibitors by phage display

S Chen, S Lovell, S Lee, M Fellner, PD Mace… - Nature …, 2021 - nature.com
Molecules that covalently bind macromolecular targets have found widespread applications
as activity-based probes and as irreversibly binding drugs. However, the general reactivity of …

Selection-based discovery of druglike macrocyclic peptides

T Passioura, T Katoh, Y Goto… - Annual review of …, 2014 - annualreviews.org
Macrocyclic peptides are an emerging class of therapeutics that can modulate protein–
protein interactions. In contrast to the heavily automated high-throughput screening systems …

Disulfide-directed multicyclic peptide libraries for the discovery of peptide ligands and drugs

S Lu, S Fan, S **ao, J Li, S Zhang, Y Wu… - Journal of the …, 2023 - ACS Publications
Multicyclic peptides with stable 3D structures are a kind of novel and promising peptide
formats for drug design and discovery as they have the potential to combine the best …