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PaperClip DNA 组装:减少、再利用、回收。

PaperClip DNA Assembly: Reduce, Reuse, Recycle.

机构信息

School of Biological Sciences, University of Edinburgh, Edinburgh, UK.

School of Engineering, University of Edinburgh, Edinburgh, UK.

出版信息

Methods Mol Biol. 2020;2205:161-177. doi: 10.1007/978-1-0716-0908-8_10.

Abstract

Creating DNA constructs is a basic and fundamental step in molecular and synthetic biology. While prices for gene synthesis are decreasing, it is still more economical in most cases to assemble constructs from a library of components (Parts). Many methods for DNA assembly are available, but most require either a fixed and inflexible format for the construct, with all Parts first being cloned in specific donor plasmids, or remaking Parts with new homology ends for each specific assembly reaction, requiring large numbers of single-use oligonucleotides. PaperClip assembly allows Parts stored in any format (linear PCR products or synthetic DNA, or cloned in any plasmid) to be used in totally flexible assembly reactions; up to 11 parts can be assembled in a single reaction, in any order, to give a linear or circular construct, and the oligonucleotides required in the assembly process can be reused in any subsequent assembly. In addition to constructing plasmids for bacterial transformation, PaperClip is also well suited to generate linear products for direct transfection of yeast, mammalian, or cyanobacterial cell lines. Thus, PaperClip offers a simple, flexible, and economical route to multipart assembly of constructs for a wide variety of purposes.

摘要

构建 DNA 构建体是分子和合成生物学的基本和基础步骤。虽然基因合成的价格在下降,但在大多数情况下,从组件(部件)库中组装构建体仍然更经济。有许多 DNA 组装方法,但大多数方法都要求构建体具有固定且不灵活的格式,所有部件首先都在特定的供体质粒中克隆,或者为每个特定的组装反应重新制作具有新同源末端的部件,需要大量的一次性寡核苷酸。PaperClip 组装允许以任何格式(线性 PCR 产物或合成 DNA,或克隆在任何质粒中)存储的部件用于完全灵活的组装反应;多达 11 个部件可以在单个反应中以任何顺序组装成线性或圆形构建体,组装过程中所需的寡核苷酸可以在任何后续组装中重复使用。除了构建用于细菌转化的质粒外,PaperClip 还非常适合生成用于直接转染酵母、哺乳动物或蓝细菌细胞系的线性产物。因此,PaperClip 为各种目的的构建体的多部件组装提供了一种简单、灵活和经济的途径。

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