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利用磁珠固定化质粒实现无细胞蛋白合成的灵活编程。

Flexible programming of cell-free protein synthesis using magnetic bead-immobilized plasmids.

机构信息

Department of Fine Chemical Engineering and Applied Chemistry, Chungnam National University, Daejeon, Korea.

出版信息

PLoS One. 2012;7(3):e34429. doi: 10.1371/journal.pone.0034429. Epub 2012 Mar 28.

Abstract

The use of magnetic bead-immobilized DNA as movable template for cell-free protein synthesis has been investigated. Magnetic microbeads containing chemically conjugated plasmids were used to direct cell-free protein synthesis, so that protein generation could be readily programmed, reset and reprogrammed. Protein synthesis by using this approach could be ON/OFF-controlled through repeated addition and removal of the microbead-conjugated DNA and employed in sequential expression of different genes in a same reaction mixture. Since the incubation periods of individual template plasmids are freely controllable, relative expression levels of multiple proteins can be tuned to desired levels. We expect that the presented results will find wide application to the flexible design and execution of synthetic pathways in cell-free chassis.

摘要

已研究将磁珠固定化 DNA 用作无细胞蛋白质合成的可移动模板。使用含有化学偶联质粒的磁性微珠来指导无细胞蛋白质合成,从而可以轻松编程、重置和重新编程蛋白质生成。通过反复添加和去除微珠偶联 DNA 来控制这种方法的蛋白质合成的开启/关闭,并在同一反应混合物中连续表达不同的基因。由于各个模板质粒的孵育期可以自由控制,因此可以将多种蛋白质的相对表达水平调节到所需水平。我们预计,所提出的结果将广泛应用于无细胞底盘中合成途径的灵活设计和执行。

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