Parallel All-Optical Assay to Study Use-Dependent Functioning of Voltage-Gated Ion Channels in a Miniaturized Format.
Algal Proteins
/ antagonists & inhibitors
Biological Assay
Calcium Channel Blockers
/ pharmacology
Calcium Channels
/ genetics
Calcium Channels, L-Type
/ genetics
Cell Line
Chlamydomonas reinhardtii
Fluorescent Dyes
/ chemistry
Gene Expression
HEK293 Cells
Humans
Intracellular Signaling Peptides and Proteins
/ antagonists & inhibitors
Ion Channel Gating
/ drug effects
Myocytes, Cardiac
/ cytology
NAV1.5 Voltage-Gated Sodium Channel
/ genetics
Nerve Tissue Proteins
/ antagonists & inhibitors
Optical Imaging
/ methods
Optogenetics
/ methods
Potassium Channel Blockers
/ pharmacology
Potassium Channels, Inwardly Rectifying
/ antagonists & inhibitors
Potassium Channels, Tandem Pore Domain
/ antagonists & inhibitors
Rhodopsin
/ antagonists & inhibitors
cardiotoxicity
high-throughput screening
ion channel
optogenetics
use dependency
Journal
SLAS discovery : advancing life sciences R & D
ISSN: 2472-5560
Titre abrégé: SLAS Discov
Pays: United States
ID NLM: 101697563
Informations de publication
Date de publication:
03 2021
03 2021
Historique:
pubmed:
19
12
2020
medline:
1
3
2022
entrez:
18
12
2020
Statut:
ppublish
Résumé
Voltage-gated ion channels produce rapid transmembrane currents responsible for action potential generation and propagation at the neuronal, muscular, and cardiac levels. They represent attractive clinical targets because their altered firing frequency is often the hallmark of pathological signaling leading to several neuromuscular disorders. Therefore, a method to study their functioning upon repeated triggers at different frequencies is desired to develop new drug molecules selectively targeting pathological phenotype. Optogenetics provides powerful tools for millisecond switch of cellular excitability in contactless, physiological, and low-cost settings. Nevertheless, its application to large-scale drug-screening operations is still limited by long processing time (due to sequential well read), rigid flashing pattern, lack of online compound addition, or high consumable costs of existing methods. Here, we developed a method that enables simultaneous analysis of 384-well plates with optical pacing, fluorescence recording, and liquid injection. We used our method to deliver programmable millisecond-switched depolarization through light-activated opsin in concomitance with continuous optical recording by a fluorescent indicator. We obtained 384-well pacing of recombinant voltage-activated sodium or calcium channels, as well as induced pluripotent stem cell (iPSC)-derived cardiomyocytes, in all-optical parallel settings. Furthermore, we demonstrated the use-dependent behavior of known ion channel blockers by optogenetic pacing at normal or pathological firing frequencies, obtaining very good signal reproducibility and accordance with electrophysiology data. Our method provides a novel physiological approach to study frequency-dependent drug behavior using reversible programmable triggers. The all-optical parallel settings combined with contained operational costs make our method particularly suited for large-scale drug-screening campaigns as well as cardiac liability studies.
Identifiants
pubmed: 33334229
doi: 10.1177/2472555220976083
pii: S2472-5552(22)06692-8
doi:
Substances chimiques
Algal Proteins
0
CACNA1D protein, human
0
CACNA2D1 protein, human
0
CACNB3 protein, human
0
Calcium Channel Blockers
0
Calcium Channels
0
Calcium Channels, L-Type
0
Fluorescent Dyes
0
Intracellular Signaling Peptides and Proteins
0
KCNJ4 protein, human
0
NAV1.5 Voltage-Gated Sodium Channel
0
Nerve Tissue Proteins
0
Potassium Channel Blockers
0
Potassium Channels, Inwardly Rectifying
0
Potassium Channels, Tandem Pore Domain
0
SCN5A protein, human
0
chlamyopsin protein, Chlamydomonas reinhardtii
0
potassium channel subfamily K member 3
1HQ3YCN4GS
Rhodopsin
9009-81-8
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM