Cargando…
A Quenched Annexin V‐Fluorophore for the Real‐Time Fluorescence Imaging of Apoptotic Processes In Vitro and In Vivo
Annexin‐based probes have long been used to study apoptotic cell death, which is of key importance to many areas of biological research, drug discovery, and clinical applications. Although apoptosis is a dynamic biological event with cell‐to‐cell variations, current annexin‐based probes are impracti...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7740095/ https://www.ncbi.nlm.nih.gov/pubmed/33344139 http://dx.doi.org/10.1002/advs.202002988 |
_version_ | 1783623451707179008 |
---|---|
author | Kim, Hyunjin Kim, Hee Yeon Lee, Eun Young Choi, Boem Kyu Jang, Hyonchol Choi, Yongdoo |
author_facet | Kim, Hyunjin Kim, Hee Yeon Lee, Eun Young Choi, Boem Kyu Jang, Hyonchol Choi, Yongdoo |
author_sort | Kim, Hyunjin |
collection | PubMed |
description | Annexin‐based probes have long been used to study apoptotic cell death, which is of key importance to many areas of biological research, drug discovery, and clinical applications. Although apoptosis is a dynamic biological event with cell‐to‐cell variations, current annexin‐based probes are impractical for monitoring apoptosis in real‐time. Herein, a quenched annexin V‐near‐infrared fluorophore conjugate (Q‐annexin V) is reported as the first OFF‐ON annexin protein‐based molecular sensor for real‐time near‐infrared fluorescence imaging of apoptosis. Q‐annexin V is non‐fluorescent in the extracellular region, due to photoinduced electron transfer interactions between the conjugated dye and amino acid quenchers (tryptophan and tyrosine). The probe becomes highly fluorescent when bound to phosphatidylserines on the outer layer of cell membranes during apoptosis, thereby enabling apoptosis to be monitored in real‐time in 2D and 3D cell structures. In particular, Q‐annexin V shows superior utility for in vivo apoptosis fluorescence imaging in animal models of cisplatin‐induced acute kidney injury and cancer immune therapy, compared to the conventional polarity‐sensitive pSIVA‐IANBD or annexin V‐Alexa647 conjugates. |
format | Online Article Text |
id | pubmed-7740095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77400952020-12-18 A Quenched Annexin V‐Fluorophore for the Real‐Time Fluorescence Imaging of Apoptotic Processes In Vitro and In Vivo Kim, Hyunjin Kim, Hee Yeon Lee, Eun Young Choi, Boem Kyu Jang, Hyonchol Choi, Yongdoo Adv Sci (Weinh) Full Papers Annexin‐based probes have long been used to study apoptotic cell death, which is of key importance to many areas of biological research, drug discovery, and clinical applications. Although apoptosis is a dynamic biological event with cell‐to‐cell variations, current annexin‐based probes are impractical for monitoring apoptosis in real‐time. Herein, a quenched annexin V‐near‐infrared fluorophore conjugate (Q‐annexin V) is reported as the first OFF‐ON annexin protein‐based molecular sensor for real‐time near‐infrared fluorescence imaging of apoptosis. Q‐annexin V is non‐fluorescent in the extracellular region, due to photoinduced electron transfer interactions between the conjugated dye and amino acid quenchers (tryptophan and tyrosine). The probe becomes highly fluorescent when bound to phosphatidylserines on the outer layer of cell membranes during apoptosis, thereby enabling apoptosis to be monitored in real‐time in 2D and 3D cell structures. In particular, Q‐annexin V shows superior utility for in vivo apoptosis fluorescence imaging in animal models of cisplatin‐induced acute kidney injury and cancer immune therapy, compared to the conventional polarity‐sensitive pSIVA‐IANBD or annexin V‐Alexa647 conjugates. John Wiley and Sons Inc. 2020-10-28 /pmc/articles/PMC7740095/ /pubmed/33344139 http://dx.doi.org/10.1002/advs.202002988 Text en © 2020 The Authors. Published by Wiley‐VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Kim, Hyunjin Kim, Hee Yeon Lee, Eun Young Choi, Boem Kyu Jang, Hyonchol Choi, Yongdoo A Quenched Annexin V‐Fluorophore for the Real‐Time Fluorescence Imaging of Apoptotic Processes In Vitro and In Vivo |
title | A Quenched Annexin V‐Fluorophore for the Real‐Time Fluorescence Imaging of Apoptotic Processes In Vitro and In Vivo |
title_full | A Quenched Annexin V‐Fluorophore for the Real‐Time Fluorescence Imaging of Apoptotic Processes In Vitro and In Vivo |
title_fullStr | A Quenched Annexin V‐Fluorophore for the Real‐Time Fluorescence Imaging of Apoptotic Processes In Vitro and In Vivo |
title_full_unstemmed | A Quenched Annexin V‐Fluorophore for the Real‐Time Fluorescence Imaging of Apoptotic Processes In Vitro and In Vivo |
title_short | A Quenched Annexin V‐Fluorophore for the Real‐Time Fluorescence Imaging of Apoptotic Processes In Vitro and In Vivo |
title_sort | quenched annexin v‐fluorophore for the real‐time fluorescence imaging of apoptotic processes in vitro and in vivo |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7740095/ https://www.ncbi.nlm.nih.gov/pubmed/33344139 http://dx.doi.org/10.1002/advs.202002988 |
work_keys_str_mv | AT kimhyunjin aquenchedannexinvfluorophorefortherealtimefluorescenceimagingofapoptoticprocessesinvitroandinvivo AT kimheeyeon aquenchedannexinvfluorophorefortherealtimefluorescenceimagingofapoptoticprocessesinvitroandinvivo AT leeeunyoung aquenchedannexinvfluorophorefortherealtimefluorescenceimagingofapoptoticprocessesinvitroandinvivo AT choiboemkyu aquenchedannexinvfluorophorefortherealtimefluorescenceimagingofapoptoticprocessesinvitroandinvivo AT janghyonchol aquenchedannexinvfluorophorefortherealtimefluorescenceimagingofapoptoticprocessesinvitroandinvivo AT choiyongdoo aquenchedannexinvfluorophorefortherealtimefluorescenceimagingofapoptoticprocessesinvitroandinvivo AT kimhyunjin quenchedannexinvfluorophorefortherealtimefluorescenceimagingofapoptoticprocessesinvitroandinvivo AT kimheeyeon quenchedannexinvfluorophorefortherealtimefluorescenceimagingofapoptoticprocessesinvitroandinvivo AT leeeunyoung quenchedannexinvfluorophorefortherealtimefluorescenceimagingofapoptoticprocessesinvitroandinvivo AT choiboemkyu quenchedannexinvfluorophorefortherealtimefluorescenceimagingofapoptoticprocessesinvitroandinvivo AT janghyonchol quenchedannexinvfluorophorefortherealtimefluorescenceimagingofapoptoticprocessesinvitroandinvivo AT choiyongdoo quenchedannexinvfluorophorefortherealtimefluorescenceimagingofapoptoticprocessesinvitroandinvivo |