VIBRANT: spectral profiling for single-cell drug responses

被引:6
|
作者
Liu, Xinwen [1 ]
Shi, Lixue [1 ,5 ,6 ]
Zhao, Zhilun [1 ]
Shu, Jian [2 ,3 ]
Min, Wei [1 ,4 ]
机构
[1] Columbia Univ, Dept Chem, New York, NY 10027 USA
[2] Harvard Med Sch, Massachusetts Gen Hosp, Cutaneous Biol Res Ctr, Boston, MA USA
[3] Broad Inst MIT & Harvard, Cambridge, MA USA
[4] Columbia Univ, Dept Biomed Engn, New York, NY 10027 USA
[5] Fudan Univ, Shanghai Xuhui Cent Hosp, Zhongshan Xuhui Hosp, Shanghai Med Coll, Shanghai, Peoples R China
[6] Fudan Univ, Inst Biomed Sci, Shanghai Med Coll, Shanghai Key Lab Med Epigenet,Int Colab Med Epigen, Shanghai, Peoples R China
基金
美国国家卫生研究院;
关键词
MASS CYTOMETRY; BREAST-CANCER; METABOLOMICS; INHIBITOR; DISCOVERY; INIPARIB; MODEL;
D O I
10.1038/s41592-024-02185-x
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
High-content cell profiling has proven invaluable for single-cell phenotyping in response to chemical perturbations. However, methods with improved throughput, information content and affordability are still needed. We present a new high-content spectral profiling method named vibrational painting (VIBRANT), integrating mid-infrared vibrational imaging, multiplexed vibrational probes and an optimized data analysis pipeline for measuring single-cell drug responses. Three infrared-active vibrational probes were designed to measure distinct essential metabolic activities in human cancer cells. More than 20,000 single-cell drug responses were collected, corresponding to 23 drug treatments. The resulting spectral profile is highly sensitive to phenotypic changes under drug perturbation. Using this property, we built a machine learning classifier to accurately predict drug mechanism of action at single-cell level with minimal batch effects. We further designed an algorithm to discover drug candidates with new mechanisms of action and evaluate drug combinations. Overall, VIBRANT has demonstrated great potential across multiple areas of phenotypic screening. Vibrational painting (VIBRANT) is a high-content single-cell phenotypic profiling method using mid-infrared imaging with vibrational probes for metabolic activity, which offers high accuracy with minimal batch effects to capture cellular responses to perturbation.
引用
收藏
页码:501 / 511
页数:24
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