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Ionophore constructed from non-covalent assembly of a G-quadruplex and liponucleoside transports K(+)-ion across biological membranes

The selective transport of ions across cell membranes, controlled by membrane proteins, is critical for a living organism. DNA-based systems have emerged as promising artificial ion transporters. However, the development of stable and selective artificial ion transporters remains a formidable task....

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Detalles Bibliográficos
Autores principales: Debnath, Manish, Chakraborty, Sandipan, Kumar, Y. Pavan, Chaudhuri, Ritapa, Jana, Biman, Dash, Jyotirmayee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6981123/
https://www.ncbi.nlm.nih.gov/pubmed/31980608
http://dx.doi.org/10.1038/s41467-019-13834-7
Descripción
Sumario:The selective transport of ions across cell membranes, controlled by membrane proteins, is critical for a living organism. DNA-based systems have emerged as promising artificial ion transporters. However, the development of stable and selective artificial ion transporters remains a formidable task. We herein delineate the construction of an artificial ionophore using a telomeric DNA G-quadruplex (h-TELO) and a lipophilic guanosine (MG). MG stabilizes h-TELO by non-covalent interactions and, along with the lipophilic side chain, promotes the insertion of h-TELO within the hydrophobic lipid membrane. Fluorescence assays, electrophysiology measurements and molecular dynamics simulations reveal that MG/h-TELO preferentially transports K(+)-ions in a stimuli-responsive manner. The preferential K(+)-ion transport is presumably due to conformational changes of the ionophore in response to different ions. Moreover, the ionophore transports K(+)-ions across CHO and K-562 cell membranes. This study may serve as a design principle to generate selective DNA-based artificial transporters for therapeutic applications.