Single cell multiplexed assay for proteolytic activity using droplet microfluidics

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• 作者：Ee Xien Ng^a ; Miles A. Miller^b ; Tengyang Jing^a ; ^c ; Chia-Hung Chen^a ; ^d ; ^{biecch@nus.edu.sg" class="auth_mail" title="E-mail the corresponding author}
• 关键词：Single cell assay ; Proteolytic activity matrix analysis ; Droplet microfluidics ; FRET-sensors
• 刊名：Biosensors and Bioelectronics
• 出版年：2016
• 出版时间：15 July 2016
• 年：2016
• 卷：81
• 期：Complete
• 页码：408-414
• 全文大小：3939 K

文摘

Cellular enzymes interact in a post-translationally regulated fashion to govern individual cell behaviors, yet current platform technologies are limited in their ability to measure multiple enzyme activities simultaneously in single cells. Here, we developed multi-color Förster resonance energy transfer (FRET)-based enzymatic substrates and use them in a microfluidics platform to simultaneously measure multiple specific protease activities from water-in-oil droplets that contain single cells. By integrating the microfluidic platform with a computational analytical method, Proteolytic Activity Matrix Analysis (PrAMA), we are able to infer six different protease activity signals from individual cells in a high throughput manner (~100 cells/experimental run). We characterized protease activity profiles at single cell resolution for several cancer cell lines including breast cancer cell line MDA-MB-231, lung cancer cell line PC-9, and leukemia cell line K-562 using both live-cell and in-situ cell lysis assay formats, with special focus on metalloproteinases important in metastasis. The ability to measure multiple proteases secreted from or expressed in individual cells allows us to characterize cell heterogeneity and has potential applications including systems biology, pharmacology, cancer diagnosis and stem cell biology.