Raman image-activated cell sorting

Author:

Nitta NaoORCID,Iino Takanori,Isozaki Akihiro,Yamagishi MaiORCID,Kitahama Yasutaka,Sakuma Shinya,Suzuki Yuta,Tezuka Hiroshi,Oikawa Minoru,Arai Fumihito,Asai Takuya,Deng Dinghuan,Fukuzawa HideyaORCID,Hase Misa,Hasunuma TomohisaORCID,Hayakawa TakeshiORCID,Hiraki Kei,Hiramatsu Kotaro,Hoshino YuORCID,Inaba Mary,Inoue Yuki,Ito TakuroORCID,Kajikawa Masataka,Karakawa Hiroshi,Kasai YusukeORCID,Kato YuichiORCID,Kobayashi HirofumiORCID,Lei Cheng,Matsusaka Satoshi,Mikami HideharuORCID,Nakagawa Atsuhiro,Numata KeijiORCID,Ota Tadataka,Sekiya Takeichiro,Shiba Kiyotaka,Shirasaki YoshitakaORCID,Suzuki Nobutake,Tanaka Shunji,Ueno Shunnosuke,Watarai Hiroshi,Yamano TakashiORCID,Yazawa Masayuki,Yonamine Yusuke,Di Carlo Dino,Hosokawa Yoichiroh,Uemura Sotaro,Sugimura Takeaki,Ozeki YasuyukiORCID,Goda KeisukeORCID

Abstract

AbstractThe advent of image-activated cell sorting and imaging-based cell picking has advanced our knowledge and exploitation of biological systems in the last decade. Unfortunately, they generally rely on fluorescent labeling for cellular phenotyping, an indirect measure of the molecular landscape in the cell, which has critical limitations. Here we demonstrate Raman image-activated cell sorting by directly probing chemically specific intracellular molecular vibrations via ultrafast multicolor stimulated Raman scattering (SRS) microscopy for cellular phenotyping. Specifically, the technology enables real-time SRS-image-based sorting of single live cells with a throughput of up to ~100 events per second without the need for fluorescent labeling. To show the broad utility of the technology, we show its applicability to diverse cell types and sizes. The technology is highly versatile and holds promise for numerous applications that are previously difficult or undesirable with fluorescence-based technologies.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

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