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Raman-Activated Droplet Sorting (RADS) for Label-Free High-Throughput Screening of Microalgal Single-Cells
Author(s) -
Xixian Wang,
Lihui Ren,
Yetian Su,
Yuetong Ji,
Yaoping Liu,
Chunyu Li,
Xunrong Li,
Yi Zhang,
Wei Wang,
Qiang Hu,
Danxiang Han,
Jian Xu,
Bo Ma
Publication year - 2017
Publication title -
analytical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.117
H-Index - 332
eISSN - 1520-6882
pISSN - 0003-2700
DOI - 10.1021/acs.analchem.7b03884
Subject(s) - chemistry , raman spectroscopy , throughput , cell sorting , sorting , microfluidics , haematococcus pluvialis , flow cytometry , nanotechnology , cell , microbiology and biotechnology , biochemistry , computer science , biology , optics , materials science , physics , telecommunications , astaxanthin , carotenoid , wireless , programming language
Raman-activated cell sorting (RACS) has attracted increasing interest, yet throughput remains one major factor limiting its broader application. Here we present an integrated Raman-activated droplet sorting (RADS) microfluidic system for functional screening of live cells in a label-free and high-throughput manner, by employing AXT-synthetic industrial microalga Haematococcus pluvialis (H. pluvialis) as a model. Raman microspectroscopy analysis of individual cells is carried out prior to their microdroplet encapsulation, which is then directly coupled to DEP-based droplet sorting. To validate the system, H. pluvialis cells containing different levels of AXT were mixed and underwent RADS. Those AXT-hyperproducing cells were sorted with an accuracy of 98.3%, an enrichment ratio of eight folds, and a throughput of ∼260 cells/min. Of the RADS-sorted cells, 92.7% remained alive and able to proliferate, which is equivalent to the unsorted cells. Thus, the RADS achieves a much higher throughput than existing RACS systems, preserves the vitality of cells, and facilitates seamless coupling with downstream manipulations such as single-cell sequencing and cultivation.

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