Tesauro Cinzia, Frøhlich Rikke, Stougaard Magnus, Ho Yi-Ping, Knudsen Birgitta R
Department of Molecular Biology and Genetics, Aarhus University, C.F. Mollers Alle 3, Building 1131, locale 328, 8000, Aarhus C, Denmark.
Department of Pathology, Aarhus University Hospital, Aarhus, Denmark.
Methods Mol Biol. 2015;1346:209-19. doi: 10.1007/978-1-4939-2987-0_14.
Cellular heterogeneity has presented a significant challenge in the studies of biology. While most of our understanding is based on the analysis of ensemble average, individual cells may process information and respond to perturbations very differently. Presented here is a highly sensitive platform capable of measuring enzymatic activity at the single-cell level. The strategy innovatively combines a rolling circle-enhanced enzyme activity detection (REEAD) assay with droplet microfluidics. The single-molecule sensitivity of REEAD allows highly sensitive detection of enzymatic activities, i.e. at the single catalytic event level, whereas the microfluidics enables isolation of single cells. Further, confined reactions in picoliter-sized droplets significantly improve enzyme extraction from human cells or microorganisms and result in faster reaction kinetics. Taken together, the described protocol is expected to open up new possibilities in the single-cell research, particularly for the elucidation of heterogeneity in a population of cells.
细胞异质性在生物学研究中提出了重大挑战。虽然我们的大部分理解基于总体平均值分析,但单个细胞处理信息和对扰动的反应可能非常不同。本文介绍了一种能够在单细胞水平测量酶活性的高灵敏度平台。该策略创新性地将滚环增强酶活性检测(REEAD)分析与液滴微流控技术相结合。REEAD的单分子灵敏度允许对酶活性进行高灵敏度检测,即在单个催化事件水平,而微流控技术能够分离单个细胞。此外,皮升大小液滴中的受限反应显著改善了从人类细胞或微生物中提取酶的效果,并导致更快的反应动力学。综上所述,所描述的方案有望在单细胞研究中开辟新的可能性,特别是用于阐明细胞群体中的异质性。