Douglas Erik S, Chandra Ravi A, Bertozzi Carolyn R, Mathies Richard A, Francis Matthew B
UCSF/UC Berkeley Joint Graduate Group in Bioengineering, University of California, Berkeley, California 94720, USA.
Lab Chip. 2007 Nov;7(11):1442-8. doi: 10.1039/b708666k. Epub 2007 Sep 19.
The successful integration of living cells into synthetic devices requires precise control over cell patterning. Here we describe a versatile platform that can accomplish this goal through DNA hybridization. Living cells functionalized with exogenous cell-surface DNA strands bind to cognate sequences of DNA printed on glass slides. Attachment via these "cell-adhesion barcodes" is rapid and specific, with close-packed arrays of cells forming within minutes. The biophysical properties of the system are characterized, and the technique is used to form complex cellular patterns with single-cell line widths and self-assembled cellular microarrays. Key advantages of DNA-directed cell binding include the ability to immobilize both adherent and non-adherent cells, to capture cells selectively from a mixed population, to tune the binding properties of the cells, and to reuse substrates prepared with widely available DNA printing technologies.
将活细胞成功整合到合成装置中需要对细胞图案化进行精确控制。在此,我们描述了一个通用平台,该平台可通过DNA杂交实现这一目标。用外源细胞表面DNA链功能化的活细胞与印在载玻片上的DNA同源序列结合。通过这些“细胞粘附条形码”进行的附着快速且特异,几分钟内即可形成紧密堆积的细胞阵列。对该系统的生物物理特性进行了表征,并利用该技术形成了具有单细胞线宽的复杂细胞图案和自组装细胞微阵列。DNA定向细胞结合的主要优点包括能够固定贴壁细胞和非贴壁细胞、从混合群体中选择性捕获细胞、调节细胞的结合特性以及重复使用采用广泛可用的DNA打印技术制备的底物。