千碱基长度单链DNA生产方法的比较

Chang-Yong Oh, E. Henderson
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引用次数: 1

摘要

DNA纳米工程,特别是DNA折纸在许多领域都有潜在的应用,例如,纳米电子学、生物医学诊断和治疗学。为了充分发挥DNA自组装在这些和其他领域的潜力,必须找到经济、可扩展和可靠的方法,从几乎任何来源生产单链DNA (ssDNA)支架。在这篇综述中,我们将描述生成ssDNA的四种策略的优点和缺点,包括滚动圈扩增(RCA),链特异性外切酶切,化学变性和不对称PCR (aPCR),并提出优化每种方法使用的方法建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Comparison of Methods for the Production of Kilobase-Length Single-Stranded DNA
DNA nanoengineering, in particular, DNA origami has potential applications in a variety of areas including, for example, nanoelectronics, biomedical diagnostics, and therapeutics. To fully realize the potential of DNA self-assembly in these and other areas, methods must be available for economical, scalable, and reliable production of single-stranded DNA (ssDNA) scaffolds from virtually any source. In this review, we will describe the virtues and liabilities of four strategies for generating ssDNA, including Rolling Circle Amplification (RCA), strand-specific exonuclease digestion, chemical denaturation, and asymmetric PCR (aPCR), with suggestions for approaches to optimize the use of each method.
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