Diversity in Genetic In Vivo Methods for Protein-Protein Interaction Studies: from the Yeast Two-Hybrid System to the Mammalian Split-Luciferase System

B Stynen, H Tournu, J Tavernier… - … and molecular biology …, 2012 - Am Soc Microbiol
The yeast two-hybrid system pioneered the field of in vivo protein-protein interaction
methods and undisputedly gave rise to a palette of ingenious techniques that are constantly …

SICLOPPS cyclic peptide libraries in drug discovery

A Tavassoli - Current Opinion in Chemical Biology, 2017 - Elsevier
Highlights•SICLOPPS allows the rapid generation of cyclic peptide libraries in cells.•A
variety of cyclic peptide ring sizes may be generated with SICLOPPS.•SICLOPPS libraries …

Biosensor-guided discovery and engineering of metabolic enzymes

HG Hwang, DY Ye, GY Jung - Biotechnology Advances, 2023 - Elsevier
A variety of chemicals have been produced through metabolic engineering approaches, and
enhancing biosynthesis performance can be achieved by using enzymes with high catalytic …

Peptides come round: using SICLOPPS libraries for early stage drug discovery

KR Lennard, A Tavassoli - Chemistry–A European Journal, 2014 - Wiley Online Library
Cyclic peptides are an emerging class of molecular therapeutics that are increasingly
viewed as ideal backbones for modulation of protein–protein interactions. A split‐intein …

Discovery of a new small-molecule inhibitor of p53–MDM2 interaction using a yeast-based approach

M Leao, C Pereira, A Bisio, Y Ciribilli, AM Paiva… - Biochemical …, 2013 - Elsevier
The virtual screening of a library of xanthone derivatives led us to the identification of
potential novel MDM2 ligands. The activity of these compounds as inhibitors of p53–MDM2 …

Identification of selective protein–protein interaction inhibitors using efficient in silico peptide-directed ligand design

AM Beekman, MMD Cominetti, SJ Walpole… - Chemical …, 2019 - pubs.rsc.org
The development of protein–protein interaction (PPI) inhibitors with therapeutic value is of
increasing importance as the first clinical agent has now been approved, but PPIs remain …

Optimized Construction of a Yeast SICLOPPS Library for Unbiased In Vivo Selection of Cyclic Peptides

N Birkmose, EU Frydendahl, CR Knudsen - Biochemistry, 2024 - ACS Publications
DNA-encoded libraries hold great potential for discovering small, cyclized peptides with
drug potential. Split-intein circular ligation of peptides and proteins (SICLOPPS) is a well …

Intracellular detection and evolution of site-specific proteases using a genetic selection system

KD Verhoeven, OC Altstadt, SN Savinov - Applied biochemistry and …, 2012 - Springer
Abstract Development of endoproteases, programmed to promote degradation of peptides
or proteins responsible for pathogenic states, represents an attractive therapeutic strategy …

Expanding the horizon of chemotherapeutic targets: from MDM2 to MDMX (MDM4)

A Macchiarulo, N Giacchè, A Carotti, F Moretti… - …, 2011 - pubs.rsc.org
Alterations of p53 signalling pathway is the most frequent event in human cancers. About
50% of these, albeit showing wild-type p53, have flaws in the control mechanisms of p53 …

Phage Display as a Combinatorial Chemistry Platform for Discovery of Chemical Structure-Activity Relationships

V Triana Guzman - 2018 - era.library.ualberta.ca
Optimization of chemical reactions, discovery of optimal substrates and determination of
substrate scope involve exhaustive screening of conditions as well as measurements of …