化学
拉曼光谱
细胞
计算生物学
核糖核酸
光学镊子
单细胞分析
纳米技术
生物化学
基因
生物
材料科学
量子力学
光学
物理
作者
Teng Fang,Wenhao Shang,Lei Zhu,Yaoyao Liu,Anpei Ye
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2020-07-09
卷期号:92 (15): 10433-10441
被引量:19
标识
DOI:10.1021/acs.analchem.0c00912
摘要
Single-cell analysis has become a state-of-art approach to heterogeneity profiling in tumor cells. Herein, we realize a kind of single-cell multimodal analytical approach by combining single-cell RNA sequencing (scRNA-seq) with Raman optical tweezers (ROT), a label-free single-cell identification and isolation technique, and apply it to investigate drug sensitivity. The drug sensitivity of human BGC823 gastric cancer cells toward different drugs, paclitaxel and sodium dichloroacetate, was distinguished in the conjoint analytical way including morphology monitoring, Raman identification, and transcriptomic profiling. Each individual BGC823 cancer cell was measured by Raman spectroscopy, then nondestructively isolated out by ROT, and finally RNA-sequenced. Our results demonstrate each analytical mode can reflect cell response to the drugs from different perspectives and is consistent and complementary with each other. Therefore, we believe the multimodal analytical approach offers an access to comprehensive characterizations of the unicellular complexity, which especially makes sense for studying tumor heterogeneity or a desired special cell from a mixture cell sample such as whole blood.
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