Quantitative analysis of drug-receptor interactions: I. Determination of kinetic and equilibrium properties

GA Weiland, PB Molinoff - Life sciences, 1981 - Elsevier
It has recently become possible to characterize a variety of different receptors by studying
the binding of appropriate drugs labelled with 3 H or 125 I. The goal of this review is to …

Snake toxins with high selectivity for subtypesof muscarinic acetylcholine receptors

E Karlsson, M Jolkkonen, E Mulugeta, P Onali, A Adem - Biochimie, 2000 - Elsevier
There are five subtypes of muscarinic acetylcholine receptors (M1 to M5) which control a
large number of physiological processes, such as the function of heart and smooth muscles …

Thermodynamic analysis of an antibody functional epitope

RF Kelley, MP O'Connell - Biochemistry, 1993 - ACS Publications
Revised Manuscript Received April 29, 1993 abstract: We have probed the relative
contribution of polar and nonpolar interactions to antibody-antigen interaction by measuring …

Fluorescent pirenzepine derivatives as potential bitopic ligands of the human M1 muscarinic receptor

C Tahtaoui, I Parrot, P Klotz, F Guillier… - Journal of medicinal …, 2004 - ACS Publications
Following a recent description of fluorescence resonance energy transfer between
enhanced green fluorescent protein (EGFP)-fused human muscarinic M1 receptors and …

Vasoactive intestinal polypeptide enhances muscarinic ligand binding in cat submandibular salivary gland

JM Lundberg, B Hedlund, T Bartfai - Nature, 1982 - nature.com
The salivary secretion from the cat submandibular salivary gland induced by
parasympathetic nerve stimulation is considered to be due to release of acetylcholine (ACh) …

[HTML][HTML] Current advances in allosteric modulation of muscarinic receptors

J Jakubik, EE El-Fakahany - Biomolecules, 2020 - mdpi.com
Allosteric modulators are ligands that bind to a site on the receptor that is spatially separated
from the orthosteric binding site for the endogenous neurotransmitter. Allosteric modulators …

Characterization of [3H](+/-) carazolol binding to beta-adrenergic receptors. Application to study of beta-adrenergic receptor subtypes in canine ventricular …

AS Manalan, HR Besch Jr, AM Watanabe - Circulation research, 1981 - Am Heart Assoc
[3H](+/-) Carazolol, a newly available beta-adrenergic receptor antagonist, can be used to
characterize beta-adrenergic receptor subtypes present in membrane vesicles derived from …

[HTML][HTML] Pirenzepine promotes the dimerization of muscarinic M1 receptors through a three-step binding process

B Ilien, N Glasser, JP Clamme, P Didier… - Journal of biological …, 2009 - ASBMB
Ligand binding to G protein-coupled receptors is a complex process that involves sequential
receptor conformational changes, ligand translocation, and possibly ligand-induced receptor …

Practical aspects of radioligand binding

M McKinney, R Raddatz - Current protocols in pharmacology, 2006 - Wiley Online Library
Radioligand binding has been used for many years to identify new binding sites,
characterize receptors, and identify novel ligands. Although various techniques have been …

Evidence of paired M2 muscarinic receptors.

LT Potter, LA Ballesteros, LH Bichajian… - Molecular …, 1991 - ASPET
Binding assays involving various antagonists, including N-[3H] methylscopolamine,[3H]
quinuclidinyl benzilate, AFDX-116, pirenzepine, and propylbenzilylcholine mustard …