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High Electrochemiluminescence from Ru(bpy)(3) (2+) Embedded Metal–Organic Frameworks to Visualize Single Molecule Movement at the Cellular Membrane

Direct imaging of single‐molecule and its movement is of fundamental importance in biology, but challenging. Herein, aided by the nanoconfinement effect and resultant high reaction activity within metal–organic frameworks (MOFs), the designed Ru(bpy)(3) (2+) embedded MOF complex (RuMOFs) exhibits br...

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Autores principales: Li, Binxiao, Huang, Xuedong, Lu, Yanwei, Fan, Zihui, Li, Bin, Jiang, Dechen, Sojic, Neso, Liu, Baohong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9762315/
https://www.ncbi.nlm.nih.gov/pubmed/36328787
http://dx.doi.org/10.1002/advs.202204715
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author Li, Binxiao
Huang, Xuedong
Lu, Yanwei
Fan, Zihui
Li, Bin
Jiang, Dechen
Sojic, Neso
Liu, Baohong
author_facet Li, Binxiao
Huang, Xuedong
Lu, Yanwei
Fan, Zihui
Li, Bin
Jiang, Dechen
Sojic, Neso
Liu, Baohong
author_sort Li, Binxiao
collection PubMed
description Direct imaging of single‐molecule and its movement is of fundamental importance in biology, but challenging. Herein, aided by the nanoconfinement effect and resultant high reaction activity within metal–organic frameworks (MOFs), the designed Ru(bpy)(3) (2+) embedded MOF complex (RuMOFs) exhibits bright electrochemiluminescence (ECL) emission permitting high‐quality imaging of ECL events at single molecule level. By labeling individual proteins of living cells with single RuMOFs, the distribution of membrane tyrosine‐protein‐kinase‐like7 (PTK7) proteins at low‐expressing cells is imaged via ECL. More importantly, the efficient capture of ECL photons generated inside the MOFs results in a stable ECL emission up to 1 h, allowing the in operando visualization of protein movements at the cellular membrane. As compared with the fluorescence observation, near‐zero ECL background surrounding the target protein with the ECL emitter gives a better contrast for the dynamic imaging of discrete protein movement. This achievement of single molecule ECL dynamic imaging using RuMOFs will provide a more effective nanoemitter to observe the distribution and motion of individual proteins at living cells.
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spelling pubmed-97623152022-12-20 High Electrochemiluminescence from Ru(bpy)(3) (2+) Embedded Metal–Organic Frameworks to Visualize Single Molecule Movement at the Cellular Membrane Li, Binxiao Huang, Xuedong Lu, Yanwei Fan, Zihui Li, Bin Jiang, Dechen Sojic, Neso Liu, Baohong Adv Sci (Weinh) Research Articles Direct imaging of single‐molecule and its movement is of fundamental importance in biology, but challenging. Herein, aided by the nanoconfinement effect and resultant high reaction activity within metal–organic frameworks (MOFs), the designed Ru(bpy)(3) (2+) embedded MOF complex (RuMOFs) exhibits bright electrochemiluminescence (ECL) emission permitting high‐quality imaging of ECL events at single molecule level. By labeling individual proteins of living cells with single RuMOFs, the distribution of membrane tyrosine‐protein‐kinase‐like7 (PTK7) proteins at low‐expressing cells is imaged via ECL. More importantly, the efficient capture of ECL photons generated inside the MOFs results in a stable ECL emission up to 1 h, allowing the in operando visualization of protein movements at the cellular membrane. As compared with the fluorescence observation, near‐zero ECL background surrounding the target protein with the ECL emitter gives a better contrast for the dynamic imaging of discrete protein movement. This achievement of single molecule ECL dynamic imaging using RuMOFs will provide a more effective nanoemitter to observe the distribution and motion of individual proteins at living cells. John Wiley and Sons Inc. 2022-11-03 /pmc/articles/PMC9762315/ /pubmed/36328787 http://dx.doi.org/10.1002/advs.202204715 Text en © 2022 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Li, Binxiao
Huang, Xuedong
Lu, Yanwei
Fan, Zihui
Li, Bin
Jiang, Dechen
Sojic, Neso
Liu, Baohong
High Electrochemiluminescence from Ru(bpy)(3) (2+) Embedded Metal–Organic Frameworks to Visualize Single Molecule Movement at the Cellular Membrane
title High Electrochemiluminescence from Ru(bpy)(3) (2+) Embedded Metal–Organic Frameworks to Visualize Single Molecule Movement at the Cellular Membrane
title_full High Electrochemiluminescence from Ru(bpy)(3) (2+) Embedded Metal–Organic Frameworks to Visualize Single Molecule Movement at the Cellular Membrane
title_fullStr High Electrochemiluminescence from Ru(bpy)(3) (2+) Embedded Metal–Organic Frameworks to Visualize Single Molecule Movement at the Cellular Membrane
title_full_unstemmed High Electrochemiluminescence from Ru(bpy)(3) (2+) Embedded Metal–Organic Frameworks to Visualize Single Molecule Movement at the Cellular Membrane
title_short High Electrochemiluminescence from Ru(bpy)(3) (2+) Embedded Metal–Organic Frameworks to Visualize Single Molecule Movement at the Cellular Membrane
title_sort high electrochemiluminescence from ru(bpy)(3) (2+) embedded metal–organic frameworks to visualize single molecule movement at the cellular membrane
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9762315/
https://www.ncbi.nlm.nih.gov/pubmed/36328787
http://dx.doi.org/10.1002/advs.202204715
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