Sasaki Naoki, Gunji Yoshitaka, Kase Chikako, Sato Kae
Department of Applied Chemistry, Faculty of Science and Engineering, Toyo University, 2100 Kujirai, Kawagoe, Saitama 350-8585, Japan.
Department of Applied Chemistry, Faculty of Science and Engineering, Toyo University, 2100 Kujirai, Kawagoe, Saitama 350-8585, Japan.
Anal Biochem. 2017 Feb 15;519:15-18. doi: 10.1016/j.ab.2016.12.002. Epub 2016 Dec 7.
Bead-based padlock rolling circle amplification (RCA), an ultrasensitive and accurate DNA detection technique, was conducted in a molecular crowding environment created by poly(ethylene glycol) (PEG). The number of RCA products generated increased and exhibited a bell-shaped dependence on PEG concentration. Experiments using magnetic beads suggested that facilitation of DNA ligation and hybridization is the main reason for the observed increase. Selectivity of the technique was retained in the presence of PEG. This technique is simple and can be utilized to detect target DNA with high accuracy and sensitivity in a variety of areas such as medical diagnosis and food analysis.
基于微珠的锁式滚环扩增(RCA)是一种超灵敏且准确的DNA检测技术,该技术在聚乙二醇(PEG)营造的分子拥挤环境中进行。所产生的RCA产物数量增加,并且呈现出对PEG浓度的钟形依赖性。使用磁珠进行的实验表明,DNA连接和杂交的促进是观察到的增加的主要原因。在PEG存在的情况下,该技术的选择性得以保留。此技术操作简单,可用于医学诊断和食品分析等多个领域中高精度、高灵敏度地检测目标DNA。