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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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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. |
format | Online Article Text |
id | pubmed-9762315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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