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...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Hyunjin, Kim, Hee Yeon, Lee, Eun Young, Choi, Boem Kyu, Jang, Hyonchol, Choi, Yongdoo
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