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Bright and Light-Up Sensing of Benzo[c,d]indole-oxazolopyridine Cyanine Dye for RNA and Its Application to Highly Sensitive Imaging of Nucleolar RNA in Living Cells
[Image: see text] Small molecular weight probes that can show a fluorescence signaling response upon binding to RNAs are promising for RNA imaging in living cells. Live-cell RNA imaging probes that can achieve a large light-up ability (>100-fold) and high Φ(bound) value for RNA (>0.50) have be...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9280936/ https://www.ncbi.nlm.nih.gov/pubmed/35847247 http://dx.doi.org/10.1021/acsomega.2c02408 |
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author | Higuchi, Kei Sato, Yusuke Togashi, Nao Suzuki, Michiyuki Yoshino, Yukina Nishizawa, Seiichi |
author_facet | Higuchi, Kei Sato, Yusuke Togashi, Nao Suzuki, Michiyuki Yoshino, Yukina Nishizawa, Seiichi |
author_sort | Higuchi, Kei |
collection | PubMed |
description | [Image: see text] Small molecular weight probes that can show a fluorescence signaling response upon binding to RNAs are promising for RNA imaging in living cells. Live-cell RNA imaging probes that can achieve a large light-up ability (>100-fold) and high Φ(bound) value for RNA (>0.50) have been rarely reported to date. Here, benzo[c,d]indole-oxazolopyridine (BIOP), an unsymmetrical monomethine cyanine analogue, was newly developed as a bright and large light-up probe for imaging of nucleolar RNA in living cells. BIOP served as a yellow-emissive probe (λ(em) = 570 nm) and exhibited a significant light-up response upon RNA binding (770-fold) with a high Φ(bound) value (0.52). We demonstrated the advantages of BIOP over a commercially available RNA-staining probe, SYTO RNA select, for robust and sensitive RNA sensing by a systematic comparison of fluorescent properties for RNA. In addition, BIOP was found to possess high membrane permeability and low cytotoxicity in living cells. The examination of live-cell imaging revealed that BIOP exhibited emission in the nucleolus upon binding to nucleolar RNA much stronger than that of SYTO RNA select. Furthermore, BIOP facilitated the highly sensitive imaging of nucleolar RNA, in which 50 nM BIOP can stain nucleolar RNA in living cells with a 20 min incubation. |
format | Online Article Text |
id | pubmed-9280936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-92809362022-07-15 Bright and Light-Up Sensing of Benzo[c,d]indole-oxazolopyridine Cyanine Dye for RNA and Its Application to Highly Sensitive Imaging of Nucleolar RNA in Living Cells Higuchi, Kei Sato, Yusuke Togashi, Nao Suzuki, Michiyuki Yoshino, Yukina Nishizawa, Seiichi ACS Omega [Image: see text] Small molecular weight probes that can show a fluorescence signaling response upon binding to RNAs are promising for RNA imaging in living cells. Live-cell RNA imaging probes that can achieve a large light-up ability (>100-fold) and high Φ(bound) value for RNA (>0.50) have been rarely reported to date. Here, benzo[c,d]indole-oxazolopyridine (BIOP), an unsymmetrical monomethine cyanine analogue, was newly developed as a bright and large light-up probe for imaging of nucleolar RNA in living cells. BIOP served as a yellow-emissive probe (λ(em) = 570 nm) and exhibited a significant light-up response upon RNA binding (770-fold) with a high Φ(bound) value (0.52). We demonstrated the advantages of BIOP over a commercially available RNA-staining probe, SYTO RNA select, for robust and sensitive RNA sensing by a systematic comparison of fluorescent properties for RNA. In addition, BIOP was found to possess high membrane permeability and low cytotoxicity in living cells. The examination of live-cell imaging revealed that BIOP exhibited emission in the nucleolus upon binding to nucleolar RNA much stronger than that of SYTO RNA select. Furthermore, BIOP facilitated the highly sensitive imaging of nucleolar RNA, in which 50 nM BIOP can stain nucleolar RNA in living cells with a 20 min incubation. American Chemical Society 2022-06-29 /pmc/articles/PMC9280936/ /pubmed/35847247 http://dx.doi.org/10.1021/acsomega.2c02408 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Higuchi, Kei Sato, Yusuke Togashi, Nao Suzuki, Michiyuki Yoshino, Yukina Nishizawa, Seiichi Bright and Light-Up Sensing of Benzo[c,d]indole-oxazolopyridine Cyanine Dye for RNA and Its Application to Highly Sensitive Imaging of Nucleolar RNA in Living Cells |
title | Bright and Light-Up Sensing of Benzo[c,d]indole-oxazolopyridine
Cyanine Dye for RNA and Its Application to
Highly Sensitive Imaging of Nucleolar RNA in Living Cells |
title_full | Bright and Light-Up Sensing of Benzo[c,d]indole-oxazolopyridine
Cyanine Dye for RNA and Its Application to
Highly Sensitive Imaging of Nucleolar RNA in Living Cells |
title_fullStr | Bright and Light-Up Sensing of Benzo[c,d]indole-oxazolopyridine
Cyanine Dye for RNA and Its Application to
Highly Sensitive Imaging of Nucleolar RNA in Living Cells |
title_full_unstemmed | Bright and Light-Up Sensing of Benzo[c,d]indole-oxazolopyridine
Cyanine Dye for RNA and Its Application to
Highly Sensitive Imaging of Nucleolar RNA in Living Cells |
title_short | Bright and Light-Up Sensing of Benzo[c,d]indole-oxazolopyridine
Cyanine Dye for RNA and Its Application to
Highly Sensitive Imaging of Nucleolar RNA in Living Cells |
title_sort | bright and light-up sensing of benzo[c,d]indole-oxazolopyridine
cyanine dye for rna and its application to
highly sensitive imaging of nucleolar rna in living cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9280936/ https://www.ncbi.nlm.nih.gov/pubmed/35847247 http://dx.doi.org/10.1021/acsomega.2c02408 |
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