Biocompatible fluorescent silicon nanocrystals for single-molecule tracking and fluorescence imaging

Author:

Nishimura Hirohito11,Ritchie Ken2,Kasai Rinshi S.1,Goto Miki1,Morone Nobuhiro1,Sugimura Hiroyuki1,Tanaka Koichiro1,Sase Ichiro3,Yoshimura Akihiko4,Nakano Yoshitaro3,Fujiwara Takahiro K.1,Kusumi Akihiro11

Affiliation:

1. Institute for Integrated Cell-Material Sciences, Institute for Frontier Medical Sciences, and Department of Materials Science and Engineering, Kyoto University, Kyoto 606-8501, Japan

2. Department of Physics, Purdue University, West Lafayette, IN 47907

3. Instruments Company, Nikon Corporation, Yokohama 244-8533, Japan

4. Department of Microbiology and Immunology, Keio University School of Medicine, Tokyo 160-8582, Japan

Abstract

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.

Publisher

Rockefeller University Press

Subject

Cell Biology

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