Angenendt Philipp, Nyarsik Lajos, Szaflarski Witold, Glökler Jörn, Nierhaus Knud H, Lehrach Hans, Cahill Dolores J, Lueking Angelika
Max-Planck-Institute for Molecular Genetics, Ihnestrasse 73, 14195 Berlin, Germany.
Anal Chem. 2004 Apr 1;76(7):1844-9. doi: 10.1021/ac035114i.
The expression and characterization of large protein libraries requires high-throughput tools for rapid and cost-effective expression and screening. A promising tool to meet these requirements is miniaturized high-density plates in chip format, consisting of an array of wells with submicroliter volumes. Here, we show the combination of nanowell chip technology and cell-free transcription and translation of proteins. Using piezoelectric dispensers, we transferred proteins into nanowells down to volumes of 100 nL and successfully detected fluorescence using confocal laser scanning. Moreover, we showed cell-free expression of proteins on a nanoliter scale using commercially available coupled transcription and translation systems. To reduce costs, we demonstrated the feasibility of diluting the coupled in vitro transcription and translation mix prior to expression. Additionally, we present an enzymatic inhibition assay in nanowells to anticipate further applications, such as the high-throughput screening of drug candidates or the identification of novel enzymes for biotechnology.
大型蛋白质文库的表达和表征需要高通量工具,以实现快速且经济高效的表达和筛选。满足这些要求的一种有前景的工具是芯片形式的小型化高密度板,它由一系列具有亚微升体积的孔组成。在此,我们展示了纳米孔芯片技术与蛋白质的无细胞转录和翻译的结合。使用压电分配器,我们将蛋白质转移到低至100 nL体积的纳米孔中,并使用共聚焦激光扫描成功检测到荧光。此外,我们使用市售的偶联转录和翻译系统展示了纳升级规模的蛋白质无细胞表达。为了降低成本,我们证明了在表达前稀释偶联的体外转录和翻译混合物的可行性。此外,我们展示了纳米孔中的酶抑制测定,以预期进一步的应用,例如药物候选物的高通量筛选或生物技术新型酶的鉴定。