[HTML][HTML] Capturing peptide–GPCR interactions and their dynamics

A Kaiser, I Coin - Molecules, 2020 - mdpi.com
Many biological functions of peptides are mediated through G protein-coupled receptors
(GPCRs). Upon ligand binding, GPCRs undergo conformational changes that facilitate the …

Oligomerization and membrane-binding properties of covalent adducts formed by the interaction of α-synuclein with the toxic dopamine metabolite 3, 4 …

C Follmer, E Coelho-Cerqueira… - Journal of Biological …, 2015 - jbc.org
Oxidative deamination of dopamine produces the highly toxic aldehyde 3, 4-
dihydroxyphenylacetaldehyde (DOPAL), enhanced production of which is found in post …

An enzyme cascade for selective modification of tyrosine residues in structurally diverse peptides and proteins

AW Struck, MR Bennett, SA Shepherd… - Journal of the …, 2016 - ACS Publications
Bioorthogonal chemistry enables a specific moiety in a complex biomolecule to be
selectively modified in the presence of many reactive functional groups and other cellular …

[HTML][HTML] A paradigm for peptide hormone-GPCR analyses

F Naider, JM Becker - Molecules, 2020 - mdpi.com
Work from our laboratories over the last 35 years that has focused on Ste2p, a G protein-
coupled receptor (GPCR), and its tridecapeptide ligand α-factor is reviewed. Our work …

The annexin I sequence Gln9-Ala10-Trp11-Phe12 is a core structure for interaction with the formyl peptide receptor 1

C Movitz, L Brive, K Hellstrand, MJ Rabiet… - Journal of Biological …, 2010 - jbc.org
The N-terminal part of the calcium-regulated and phospholipid-binding protein annexin AI
contains peptide sequences with pro-and anti-inflammatory activities. We have earlier …

Hydrogen/deuterium exchange of cross-linkable α-amino acid derivatives in deuterated triflic acid

L Wang, Y Murai, T Yoshida, M Okamoto… - Bioscience …, 2014 - academic.oup.com
In this paper we report here a hydrogen/deuterium exchange (H/D exchange) of cross-
linkable α-amino acid derivatives with deuterated trifluoromethanesulfonic acid (TfOD). H/D …

Differential interactions of fluorescent agonists and antagonists with the yeast G protein coupled receptor Ste2p

E Mathew, A Bajaj, SM Connelly, H Sargsyan… - Journal of molecular …, 2011 - Elsevier
We describe a rapid method to probe for mutations in cell surface ligand-binding proteins
that affect the environment of bound ligand. The method uses fluorescence-activated cell …

Bio-orthogonal and combinatorial approaches for the design of binding growth factors

Y Ito, S Tada - Biomaterials, 2013 - Elsevier
Merrifield chemistry enables the convenient synthesis of oligonucleotides and peptides,
while recombinant DNA technology has facilitated protein engineering. Recently, protein …

Identification of residue-to-residue contact between a peptide ligand and its G protein-coupled receptor using periodate-mediated dihydroxyphenylalanine cross …

GKE Umanah, L Huang, F Ding, B Arshava… - Journal of Biological …, 2010 - jbc.org
Fundamental knowledge about how G protein-coupled receptors and their ligands interact is
important for understanding receptor-ligand binding and the development of new drug …

Binding of fluorinated phenylalanine α-factor analogues to ste2p: Evidence for a cation− π binding interaction between a peptide ligand and its cognate G protein …

S Tantry, FX Ding, M Dumont, JM Becker, F Naider - Biochemistry, 2010 - ACS Publications
Ste2p, a G protein-coupled receptor (GPCR), binds α-factor, WHWLQLKPGQPMY, a
tridecapeptide pheromone secreted by yeast cells. Upon α-factor binding, Ste2p undergoes …