| Literature DB >> 27922213 |
Maxime Rossato1, Guillaume Miralles1, Céline M'Kadmi1, Mathieu Maingot1, Muriel Amblard1, Bernard Mouillac2, Didier Gagne1, Jean Martinez1, Gilles Subra1, Christine Enjalbal1, Sonia Cantel1.
Abstract
Radiolabeling of ligands is still the gold standard in the study of high-affinity receptor-ligand interactions. In an effort toward safer and simpler alternatives to the use of radioisotopes, we developed a quantitative and highly sensitive matrix-assisted laser desorption ionization mass spectrometry (MALDI-MS) method that relies on the use of chemically tagged ligands designed to be specifically detectable when present as traces in complex biological mixtures such as cellular lysates. This innovative technology allows easy, sensitive detection and accurate quantification of analytes at the sub-nanomolar level. After statistical validation, we were able to perform pharmacological evaluations of G protein-coupled receptor (V1A-R)-ligand interactions. Both saturation and competitive binding assays were successfully processed.Entities:
Keywords: CHCA labeling; MALDI mass spectrometry; MS binding assays; peptide ligands; quantification; stable isotope dilution
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Year: 2016 PMID: 27922213 DOI: 10.1002/cmdc.201600447
Source DB: PubMed Journal: ChemMedChem ISSN: 1860-7179 Impact factor: 3.466