Department of Pharmaceutical Chemistry, University of California, San Francisco, CA 94143.
Department of Bioengineering and Therapeutic Sciences, California Institute for Quantitative Biosciences, University of California, San Francisco, CA 94158.
Proc Natl Acad Sci U S A. 2017 Aug 15;114(33):8728-8733. doi: 10.1073/pnas.1704020114. Epub 2017 Jul 31.
Although the elementary unit of biology is the cell, high-throughput methods for the microscale manipulation of cells and reagents are limited. The existing options either are slow, lack single-cell specificity, or use fluid volumes out of scale with those of cells. Here we present printed droplet microfluidics, a technology to dispense picoliter droplets and cells with deterministic control. The core technology is a fluorescence-activated droplet sorter coupled to a specialized substrate that together act as a picoliter droplet and single-cell printer, enabling high-throughput generation of intricate arrays of droplets, cells, and microparticles. Printed droplet microfluidics provides a programmable and robust technology to construct arrays of defined cell and reagent combinations and to integrate multiple measurement modalities together in a single assay.
虽然生物学的基本单位是细胞,但用于微尺度操控细胞和试剂的高通量方法却很有限。现有的方法要么速度慢,缺乏单细胞特异性,要么使用的流体体积与细胞体积不成比例。在这里,我们提出了印刷液滴微流控技术,这是一种能够以确定的控制方式分配皮升级液滴和细胞的技术。核心技术是一种与专门的基底结合的荧光激活液滴分选器,它共同作用形成皮升级液滴和单细胞打印机,从而能够高通量地生成复杂的液滴、细胞和微颗粒阵列。印刷液滴微流控技术为构建定义明确的细胞和试剂组合阵列以及在单个测定中整合多种测量模式提供了一种可编程和强大的技术。