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Biocompatible fluorescent silicon nanocrystals for single-molecule tracking and fluorescence imaging
Fluorescence microscopy is used extensively in cell-biological and biomedical research, but it is often plagued by three major problems with the presently available fluorescent probes: photobleaching, blinking, and large size. We have addressed these problems, with special attention to single-molecu...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3776351/ https://www.ncbi.nlm.nih.gov/pubmed/24043702 http://dx.doi.org/10.1083/jcb.201301053 |
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author | Nishimura, Hirohito Ritchie, Ken Kasai, Rinshi S. Goto, Miki Morone, Nobuhiro Sugimura, Hiroyuki Tanaka, Koichiro Sase, Ichiro Yoshimura, Akihiko Nakano, Yoshitaro Fujiwara, Takahiro K. Kusumi, Akihiro |
author_facet | Nishimura, Hirohito Ritchie, Ken Kasai, Rinshi S. Goto, Miki Morone, Nobuhiro Sugimura, Hiroyuki Tanaka, Koichiro Sase, Ichiro Yoshimura, Akihiko Nakano, Yoshitaro Fujiwara, Takahiro K. Kusumi, Akihiro |
author_sort | Nishimura, Hirohito |
collection | PubMed |
description | Fluorescence microscopy is used extensively in cell-biological and biomedical research, but it is often plagued by three major problems with the presently available fluorescent probes: photobleaching, blinking, and large size. We have addressed these problems, with special attention to single-molecule imaging, by developing biocompatible, red-emitting silicon nanocrystals (SiNCs) with a 4.1-nm hydrodynamic diameter. Methods for producing SiNCs by simple chemical etching, for hydrophilically coating them, and for conjugating them to biomolecules precisely at a 1:1 ratio have been developed. Single SiNCs neither blinked nor photobleached during a 300-min overall period observed at video rate. Single receptor molecules in the plasma membrane of living cells (using transferrin receptor) were imaged for ≥10 times longer than with other probes, making it possible for the first time to observe the internalization process of receptor molecules at the single-molecule level. Spatial variations of molecular diffusivity in the scale of 1–2 µm, i.e., a higher level of domain mosaicism in the plasma membrane, were revealed. |
format | Online Article Text |
id | pubmed-3776351 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-37763512014-03-16 Biocompatible fluorescent silicon nanocrystals for single-molecule tracking and fluorescence imaging Nishimura, Hirohito Ritchie, Ken Kasai, Rinshi S. Goto, Miki Morone, Nobuhiro Sugimura, Hiroyuki Tanaka, Koichiro Sase, Ichiro Yoshimura, Akihiko Nakano, Yoshitaro Fujiwara, Takahiro K. Kusumi, Akihiro J Cell Biol Research Articles Fluorescence microscopy is used extensively in cell-biological and biomedical research, but it is often plagued by three major problems with the presently available fluorescent probes: photobleaching, blinking, and large size. We have addressed these problems, with special attention to single-molecule imaging, by developing biocompatible, red-emitting silicon nanocrystals (SiNCs) with a 4.1-nm hydrodynamic diameter. Methods for producing SiNCs by simple chemical etching, for hydrophilically coating them, and for conjugating them to biomolecules precisely at a 1:1 ratio have been developed. Single SiNCs neither blinked nor photobleached during a 300-min overall period observed at video rate. Single receptor molecules in the plasma membrane of living cells (using transferrin receptor) were imaged for ≥10 times longer than with other probes, making it possible for the first time to observe the internalization process of receptor molecules at the single-molecule level. Spatial variations of molecular diffusivity in the scale of 1–2 µm, i.e., a higher level of domain mosaicism in the plasma membrane, were revealed. The Rockefeller University Press 2013-09-16 /pmc/articles/PMC3776351/ /pubmed/24043702 http://dx.doi.org/10.1083/jcb.201301053 Text en © 2013 Nishimura et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Nishimura, Hirohito Ritchie, Ken Kasai, Rinshi S. Goto, Miki Morone, Nobuhiro Sugimura, Hiroyuki Tanaka, Koichiro Sase, Ichiro Yoshimura, Akihiko Nakano, Yoshitaro Fujiwara, Takahiro K. Kusumi, Akihiro Biocompatible fluorescent silicon nanocrystals for single-molecule tracking and fluorescence imaging |
title | Biocompatible fluorescent silicon nanocrystals for single-molecule tracking and fluorescence imaging |
title_full | Biocompatible fluorescent silicon nanocrystals for single-molecule tracking and fluorescence imaging |
title_fullStr | Biocompatible fluorescent silicon nanocrystals for single-molecule tracking and fluorescence imaging |
title_full_unstemmed | Biocompatible fluorescent silicon nanocrystals for single-molecule tracking and fluorescence imaging |
title_short | Biocompatible fluorescent silicon nanocrystals for single-molecule tracking and fluorescence imaging |
title_sort | biocompatible fluorescent silicon nanocrystals for single-molecule tracking and fluorescence imaging |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3776351/ https://www.ncbi.nlm.nih.gov/pubmed/24043702 http://dx.doi.org/10.1083/jcb.201301053 |
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