Chen Bob, Lim Sungwon, Kannan Arvind, Alford Spencer C, Sunden Fanny, Herschlag Daniel, Dimov Ivan K, Baer Thomas M, Cochran Jennifer R
Department of Bioengineering, Stanford University, Stanford, California, USA.
Department of Chemical Engineering, Stanford University, Stanford, California, USA.
Nat Chem Biol. 2016 Feb;12(2):76-81. doi: 10.1038/nchembio.1978. Epub 2015 Dec 7.
We describe a multipurpose technology platform, termed μSCALE (microcapillary single-cell analysis and laser extraction), that enables massively parallel, quantitative biochemical and biophysical measurements on millions of protein variants expressed from yeast or bacteria. μSCALE spatially segregates single cells within a microcapillary array, enabling repeated imaging, cell growth and protein expression. We performed high-throughput analysis of cells and their protein products using a range of fluorescent assays, including binding-affinity measurements and dynamic enzymatic assays. A precise laser-based extraction method allows rapid recovery of live clones and their genetic material from microcapillaries for further study. With μSCALE, we discovered a new antibody against a clinical cancer target, evolved a fluorescent protein biosensor and engineered an enzyme to reduce its sensitivity to its inhibitor. These protein analysis and engineering applications each have unique assay requirements and different host organisms, highlighting the flexibility and technical capabilities of the μSCALE platform.
我们描述了一种多功能技术平台,称为μSCALE(微毛细管单细胞分析与激光提取),它能够对数百万个由酵母或细菌表达的蛋白质变体进行大规模并行、定量的生化和生物物理测量。μSCALE在微毛细管阵列中对单细胞进行空间分离,实现重复成像、细胞生长和蛋白质表达。我们使用一系列荧光检测方法,包括结合亲和力测量和动态酶检测,对细胞及其蛋白质产物进行了高通量分析。一种精确的基于激光的提取方法允许从微毛细管中快速回收活克隆及其遗传物质,以供进一步研究。借助μSCALE,我们发现了一种针对临床癌症靶点的新抗体,改进了一种荧光蛋白生物传感器,并改造了一种酶以降低其对抑制剂的敏感性。这些蛋白质分析和工程应用各自具有独特的检测要求和不同的宿主生物体,突出了μSCALE平台的灵活性和技术能力。