Cargando…
Covalent Modification of Mutant Rat P2X2 Receptors with a Thiol-Reactive Fluorophore Allows Channel Activation by Zinc or Acidic pH without ATP
Rat P2X2 receptors open at an undetectably low rate in the absence of ATP. Furthermore, two allosteric modulators, zinc and acidic pH, cannot by themselves open these channels. We describe here the properties of a mutant receptor, K69C, before and after treatment with the thiol-reactive fluorophore...
Autores principales: | Dellal, Shlomo S., Hume, Richard I. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3480388/ https://www.ncbi.nlm.nih.gov/pubmed/23112811 http://dx.doi.org/10.1371/journal.pone.0047147 |
Ejemplares similares
-
Covalent and non-covalent coupling of a Au(102) nanocluster with a fluorophore: energy transfer, quenching and intracellular pH sensing
por: Hulkko, Eero, et al.
Publicado: (2021) -
Azidobupramine, an Antidepressant-Derived Bifunctional Neurotransmitter Transporter Ligand Allowing Covalent Labeling and Attachment of Fluorophores
por: Kirmeier, Thomas, et al.
Publicado: (2016) -
Color-Tunable Indolizine-Based Fluorophores and Fluorescent pH Sensor
por: Kim, Taegwan, et al.
Publicado: (2021) -
Methyltransferase-directed covalent coupling of fluorophores to DNA
por: Lauer, Milena Helmer, et al.
Publicado: (2017) -
Amino-isocyanoacridines: Novel, Tunable Solvatochromic Fluorophores as Physiological pH Probes
por: Nagy, Miklós, et al.
Publicado: (2019)