Long-Lived States in Hyperpolarized Deuterated Methyl Groups Reveal Weak Binding of Small Molecules to Proteins.
Journal
The journal of physical chemistry letters
ISSN: 1948-7185
Titre abrégé: J Phys Chem Lett
Pays: United States
ID NLM: 101526034
Informations de publication
Date de publication:
04 Apr 2019
04 Apr 2019
Historique:
pubmed:
14
3
2019
medline:
19
4
2019
entrez:
14
3
2019
Statut:
ppublish
Résumé
We introduce a method for the detection of weak interactions of small molecules such as metabolites or medicaments that contain deuterated methyl groups with proteins in solution. The technique relies on long-lived imbalances of spin state populations, which are generated by dissolution dynamic nuclear polarization (D-DNP) and feature lifetimes that depend on the frequency of internal rotation of deuterated methyl groups. We demonstrate the technique for interactions between deuterated dimethyl sulfoxide (DMSO- d
Identifiants
pubmed: 30864805
doi: 10.1021/acs.jpclett.9b00149
doi:
Substances chimiques
Serum Albumin, Bovine
27432CM55Q
Deuterium
AR09D82C7G
Trypsin
EC 3.4.21.4
Dimethyl Sulfoxide
YOW8V9698H
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM