TY - JOUR
T1 - Raman-Activated Droplet Sorting (RADS) for Label-Free High-Throughput Screening of Microalgal Single-Cells
AU - Wang, Xixian
AU - Ren, Lihui
AU - Su, Yetian
AU - Ji, Yuetong
AU - Liu, Yaoping
AU - Li, Chunyu
AU - Li, Xunrong
AU - Zhang, Yi
AU - Wang, Wei
AU - Hu, Qiang
AU - Han, Danxiang
AU - Xu, Jian
AU - Ma, Bo
N1 - Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/11/21
Y1 - 2017/11/21
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/85035036749
U2 - 10.1021/acs.analchem.7b03884
DO - 10.1021/acs.analchem.7b03884
M3 - 文章
C2 - 29099582
AN - SCOPUS:85035036749
SN - 0003-2700
VL - 89
SP - 12569
EP - 12577
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 22
ER -