Single-Cell Digital Microfluidic Mass Spectrometry Platform for Efficient and Multiplex Genotyping of Circulating Tumor Cells

Gene mutation profiling of heterogeneous circulating tumor cells (CTCs) offers comprehensive and real-time molecular information of tumors for targeted therapy guidance, but the lack of efficient and multiplex genotyping techniques for single-CTC analysis greatly hinders its development and clinical...

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Veröffentlicht in:Analytical chemistry (Washington) 2022-01, Vol.94 (2), p.1108-1117
Hauptverfasser: Ruan, Qingyu, Yang, Jian, Zou, Fenxiang, Chen, Xiaofeng, Zhang, Qianqian, Zhao, Kaifeng, Lin, Xiaoye, Zeng, Xi, Yu, Xiyuan, Wu, Lingling, Lin, Shuichao, Zhu, Zhi, Yang, Chaoyong
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container_issue 2
container_start_page 1108
container_title Analytical chemistry (Washington)
container_volume 94
creator Ruan, Qingyu
Yang, Jian
Zou, Fenxiang
Chen, Xiaofeng
Zhang, Qianqian
Zhao, Kaifeng
Lin, Xiaoye
Zeng, Xi
Yu, Xiyuan
Wu, Lingling
Lin, Shuichao
Zhu, Zhi
Yang, Chaoyong
description Gene mutation profiling of heterogeneous circulating tumor cells (CTCs) offers comprehensive and real-time molecular information of tumors for targeted therapy guidance, but the lack of efficient and multiplex genotyping techniques for single-CTC analysis greatly hinders its development and clinical application. This paper reports a single-CTC mass spectrometry analysis method for efficient and multiplex mutation profiling based on digital microfluidics. Digital microfluidics affords integrated single-CTC manipulation, from single-CTC isolation to high-performance whole genome amplification, via nanoliter droplet-based wettability trapping and hydrodynamic adjustment of cell distribution. Coupled with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, multiplex mutation information of individual CTCs can be efficiently and accurately identified by the inherent mass differences of different DNA sequences. This platform achieves Kirsten rat sarcoma viral oncogene mutation profiling of heterogeneous CTCs at the single-cell level from cancer patient samples, offering new avenues for genotype profiling of single CTCs and cancer therapy guidance.
doi_str_mv 10.1021/acs.analchem.1c04194
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Chem</addtitle><description>Gene mutation profiling of heterogeneous circulating tumor cells (CTCs) offers comprehensive and real-time molecular information of tumors for targeted therapy guidance, but the lack of efficient and multiplex genotyping techniques for single-CTC analysis greatly hinders its development and clinical application. This paper reports a single-CTC mass spectrometry analysis method for efficient and multiplex mutation profiling based on digital microfluidics. Digital microfluidics affords integrated single-CTC manipulation, from single-CTC isolation to high-performance whole genome amplification, via nanoliter droplet-based wettability trapping and hydrodynamic adjustment of cell distribution. Coupled with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, multiplex mutation information of individual CTCs can be efficiently and accurately identified by the inherent mass differences of different DNA sequences. 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subjects Analytical chemistry
Cancer
Cell Line, Tumor
Cell Separation - methods
Chemistry
Deoxyribonucleic acid
DNA
Gene sequencing
Genomes
Genotype
Genotypes
Genotyping
Humans
Ionization
Ions
Mass Spectrometry
Mass spectroscopy
Microfluidics
Microfluidics - methods
Multiplexing
Mutation
Neoplastic Cells, Circulating - pathology
Nucleotide sequence
Point mutation
Sarcoma
Scientific imaging
Single-Cell Analysis - methods
Spectroscopy
Tumor cells
Tumors
Wettability
title Single-Cell Digital Microfluidic Mass Spectrometry Platform for Efficient and Multiplex Genotyping of Circulating Tumor Cells
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