National Cancer Institute, National Institutes of Health, Bethesda, MD, United States of America.
Department of Mechanical Engineering, University of Maryland, College Park, MD, United States of America.
Biofabrication. 2021 Jul 20;13(4). doi: 10.1088/1758-5090/ac1258.
Selective spatial isolation and manipulation of single chromosomes and the controlled formation of defined chromosome ensembles in a droplet-based microfluidic system is presented. The multifunctional microfluidic technology employs elastomer valves and membrane displacement traps to support deterministic manipulation of individual droplets. Picoliter droplets are formed in the 2D array of microscale traps by self-discretization of a nanoliter sample plug, with membranes positioned over each trap allowing controllable metering or full release of selected droplets. By combining discretization, optical interrogation, and selective droplet release for sequential delivery to a downstream merging zone, the system enables efficient manipulation of multiple chromosomes into a defined ensemble with single macromolecule resolution. Key design and operational parameters are explored, and co-compartmentalization of three chromosome pairs is demonstrated as a first step toward formation of precisely defined chromosome ensembles for applications in genetic engineering and synthetic biology.
本文提出了一种基于液滴微流控系统的单染色体选择性空间隔离和操作,以及定义染色体组合的可控形成。这种多功能微流控技术采用弹性体阀和膜位移阱来支持单个液滴的确定性操作。皮升液滴通过纳升级样品塞的自离散化在微尺度阱的 2D 阵列中形成,每个阱上方的膜允许对选定的液滴进行可控计量或完全释放。通过离散化、光学检测以及选择性释放液滴以顺序递送至下游合并区,该系统可实现对多个染色体进行高效操作,形成具有单大分子分辨率的定义明确的染色体组合。本文探索了关键的设计和操作参数,并演示了三个染色体对的共 compartmentalization,作为用于遗传工程和合成生物学的精确定义染色体组合形成的第一步。