Kurita Hirofumi, Inaishi Ken-ichi, Torii Ken, Urisu Madoka, Nakano Michihiko, Katsura Shinji, Mizuno Akira
Department of Ecological Engineering, Toyohashi University of Technology, Aichi 441-8580, Japan.
J Biomol Struct Dyn. 2008 Apr;25(5):473-80. doi: 10.1080/07391102.2008.10507194.
Single-molecule DNA digestion by exonuclease III, which has 3' to 5' exonuclease activity, was analyzed using a micro-channel with two-layer laminar flow. First, a DNA-bead complex was optically trapped in one layer in the absence of exonuclease III permitted the DNA to be stretched by the laminar flow. The exonuclease III reaction was initiated by moving the trapped DNA-bead complex to another layer of flow, which contained exonuclease III. As the reaction proceeded, the fluorescently-stained DNA was observed to shorten. The process was photographed; examination of the photographs showed that the DNA molecule shortened in a linear fashion with respect to the reaction time. The digestion rate obtained from the single-molecule experiment was compared to that measured from a bulk experiment and was found to be ca. 28 times higher than the bulk digestion rate.
使用具有3'至5'核酸外切酶活性的核酸外切酶III对单分子DNA进行消化,并通过具有两层层流的微通道进行分析。首先,在不存在核酸外切酶III的情况下,将DNA-珠子复合物光学捕获在一层中,使DNA被层流拉伸。通过将捕获的DNA-珠子复合物移动到含有核酸外切酶III的另一层流中来启动核酸外切酶III反应。随着反应的进行,观察到荧光染色的DNA缩短。对该过程进行拍照;对照片的检查表明,DNA分子相对于反应时间呈线性缩短。将单分子实验获得的消化率与批量实验测量的消化率进行比较,发现前者约为后者的28倍。