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High-throughput label-free molecular fingerprinting flow cytometry.
Hiramatsu, Kotaro; Ideguchi, Takuro; Yonamine, Yusuke; Lee, SangWook; Luo, Yizhi; Hashimoto, Kazuki; Ito, Takuro; Hase, Misa; Park, Jee-Woong; Kasai, Yusuke; Sakuma, Shinya; Hayakawa, Takeshi; Arai, Fumihito; Hoshino, Yu; Goda, Keisuke.
Afiliación
  • Hiramatsu K; Department of Chemistry, The University of Tokyo, Tokyo 113-0033, Japan.
  • Ideguchi T; Research Centre for Spectrochemistry, The University of Tokyo, Tokyo 113-0033, Japan.
  • Yonamine Y; PRESTO, Japan Science and Technology Agency, Saitama 332-0012, Japan.
  • Lee S; Research Centre for Spectrochemistry, The University of Tokyo, Tokyo 113-0033, Japan.
  • Luo Y; PRESTO, Japan Science and Technology Agency, Saitama 332-0012, Japan.
  • Hashimoto K; Department of Physics, The University of Tokyo, Tokyo 113-0033, Japan.
  • Ito T; Department of Chemical Engineering, Kyushu University, Fukuoka 819-0395, Japan.
  • Hase M; Department of Chemistry, The University of Tokyo, Tokyo 113-0033, Japan.
  • Park JW; Department of Chemistry, The University of Tokyo, Tokyo 113-0033, Japan.
  • Kasai Y; Department of Chemistry, The University of Tokyo, Tokyo 113-0033, Japan.
  • Sakuma S; Department of Chemistry, The University of Tokyo, Tokyo 113-0033, Japan.
  • Hayakawa T; Japan Science and Technology Agency, Saitama 332-0012, Japan.
  • Arai F; Department of Chemistry, The University of Tokyo, Tokyo 113-0033, Japan.
  • Hoshino Y; Department of Chemistry, The University of Tokyo, Tokyo 113-0033, Japan.
  • Goda K; Department of Micro-Nano Mechanical Science and Engineering, Nagoya University, Aichi 464-8603, Japan.
Sci Adv ; 5(1): eaau0241, 2019 01.
Article en En | MEDLINE | ID: mdl-30746443
ABSTRACT
Flow cytometry is an indispensable tool in biology for counting and analyzing single cells in large heterogeneous populations. However, it predominantly relies on fluorescent labeling to differentiate cells and, hence, comes with several fundamental drawbacks. Here, we present a high-throughput Raman flow cytometer on a microfluidic chip that chemically probes single live cells in a label-free manner. It is based on a rapid-scan Fourier-transform coherent anti-Stokes Raman scattering spectrometer as an optical interrogator, enabling us to obtain the broadband molecular vibrational spectrum of every single cell in the fingerprint region (400 to 1600 cm-1) with a record-high throughput of ~2000 events/s. As a practical application of the method not feasible with conventional flow cytometry, we demonstrate high-throughput label-free single-cell analysis of the astaxanthin productivity and photosynthetic dynamics of Haematococcus lacustris.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Espectrometría Raman / Citometría de Flujo Idioma: En Revista: Sci Adv Año: 2019 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Espectrometría Raman / Citometría de Flujo Idioma: En Revista: Sci Adv Año: 2019 Tipo del documento: Article País de afiliación: Japón
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