| Literature DB >> 34767659 |
Yousef Bagheri1, Ahsan Ausaf Ali1, Puspam Keshri1, James Chambers2, Anne Gershenson3, Mingxu You1.
Abstract
The cell membrane is a dynamic and heterogeneous structure composed of distinct sub-compartments. Within these compartments, preferential interactions occur among various lipids and proteins. Currently, it is still challenging to image these short-lived membrane complexes, especially in living cells. In this work, we present a DNA-based probe, termed "DNA Zipper", which allows the membrane order and pattern of transient interactions to be imaged in living cells using standard fluorescence microscopes. By fine-tuning the length and binding affinity of DNA duplex, these probes can precisely extend the duration of membrane lipid interactions via dynamic DNA hybridization. The correlation between membrane order and the activation of T-cell receptor signaling has also been studied. These programmable DNA probes function after a brief cell incubation, which can be easily adapted to study lipid interactions and membrane order during different membrane signaling events.Entities:
Keywords: DNA probes; FRET; T-cell activation; cell membrane imaging; membrane order
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Year: 2021 PMID: 34767659 PMCID: PMC8792286 DOI: 10.1002/anie.202112033
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336