Department of Chemistry, University of North Carolina, Chapel Hill, NC 27599, USA.
Analyst. 2013 Jan 7;138(1):220-8. doi: 10.1039/c2an36065a. Epub 2012 Oct 25.
A microengineered array to sample clonal colonies is described. The cells were cultured on an array of individually releasable elements until the colonies expanded to cover multiple elements. Single elements were released using a laser-based system and collected to sample cells from individual colonies. A greater than an 85% rate in splitting and collecting colonies was achieved using a 3-dimensional cup-like design or "microcup". Surface modification using patterned titanium deposition of the glass substrate improved the stability of microcup adhesion to the glass while enabling minimization of the laser energy for splitting the colonies. Smaller microcup dimensions and slotting the microcup walls reduced the time needed for colonies to expand into multiple microcups. The stem cell colony retained on the array and the collected fraction within released microcups remained undifferentiated and viable. The colony samples were characterized by both reporter gene expression and a destructive assay (PCR) to identify target colonies. The platform is envisioned as a means to rapidly establish cell lines using a destructive assay to identify desired clones.
本文描述了一种用于采集克隆菌落的微工程化阵列。细胞在可单独释放的元件阵列上培养,直到菌落扩展覆盖多个元件。使用基于激光的系统释放单个元件,并将其收集以从单个菌落中取样细胞。使用三维杯状设计或“微杯”实现了大于 85%的分裂和收集菌落的速率。通过在玻璃基板上进行图案化钛沉积进行表面改性,提高了微杯与玻璃的附着力的稳定性,同时最小化了用于分裂菌落的激光能量。较小的微杯尺寸和微杯壁开槽减少了菌落扩展到多个微杯所需的时间。保留在阵列上的干细胞菌落和收集的释放微杯内的部分保持未分化和存活状态。通过报告基因表达和破坏性测定(PCR)对菌落样本进行了特征分析,以鉴定目标菌落。该平台旨在通过破坏性测定快速建立细胞系,以鉴定所需的克隆。