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单分子DNA测序的进展:单色演示

Progress towards single-molecule DNA sequencing: a one color demonstration.

作者信息

Werner James H, Cai Hong, Jett James H, Reha-Krantz Linda, Keller Richard A, Goodwin Peter M

机构信息

Bioscience Division, Los Alamos National Laboratory, Mail Stop J586, Los Alamos, NM 87545, USA.

出版信息

J Biotechnol. 2003 Apr 10;102(1):1-14. doi: 10.1016/s0168-1656(03)00006-3.

Abstract

Single molecules of fluorescently labeled nucleotides were detected during the cleavage of individual DNA fragments by a processive exonuclease. In these experiments, multiple (10-100) strands of DNA with tetramethyl rhodamine labeled dUMP (TMR-dUMP) incorporated into the sequence were anchored in flow upstream of the detection region of an ultra sensitive flow cytometer. A dilute solution of Exonuclease I passed over the microspheres. When an exonuclease attached to a strand, processive digestion of that strand began. The liberated, labeled bases flowed through the detection region and were detected at high efficiency at the single-molecule level by laser-induced fluorescence. The digestion of a single strand of DNA by a single exonuclease was discernable in these experiments. This result demonstrates the feasibility of single-molecule DNA sequencing. In addition, these experiments point to a new and practical means of arriving at a consensus sequence by individually reading out identical sequences on multiple fragments.

摘要

在单个DNA片段被连续外切核酸酶切割的过程中,检测到了荧光标记核苷酸的单分子。在这些实验中,将多个(10 - 100个)掺入了四甲基罗丹明标记的dUMP(TMR - dUMP)的DNA链固定在超灵敏流式细胞仪检测区域上游的流体中。外切核酸酶I的稀溶液流过微球。当一个外切核酸酶附着到一条链上时,该链的连续消化就开始了。释放出的标记碱基流过检测区域,并通过激光诱导荧光在单分子水平上被高效检测到。在这些实验中,可以辨别出单个外切核酸酶对单条DNA链的消化。这一结果证明了单分子DNA测序的可行性。此外,这些实验还指出了一种新的实用方法,即通过分别读出多个片段上的相同序列来获得一致序列。

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