Eid John, Fehr Adrian, Gray Jeremy, Luong Khai, Lyle John, Otto Geoff, Peluso Paul, Rank David, Baybayan Primo, Bettman Brad, Bibillo Arkadiusz, Bjornson Keith, Chaudhuri Bidhan, Christians Frederick, Cicero Ronald, Clark Sonya, Dalal Ravindra, Dewinter Alex, Dixon John, Foquet Mathieu, Gaertner Alfred, Hardenbol Paul, Heiner Cheryl, Hester Kevin, Holden David, Kearns Gregory, Kong Xiangxu, Kuse Ronald, Lacroix Yves, Lin Steven, Lundquist Paul, Ma Congcong, Marks Patrick, Maxham Mark, Murphy Devon, Park Insil, Pham Thang, Phillips Michael, Roy Joy, Sebra Robert, Shen Gene, Sorenson Jon, Tomaney Austin, Travers Kevin, Trulson Mark, Vieceli John, Wegener Jeffrey, Wu Dawn, Yang Alicia, Zaccarin Denis, Zhao Peter, Zhong Frank, Korlach Jonas, Turner Stephen
Pacific Biosciences, 1505 Adams Drive, Menlo Park, CA 94025, USA.
Science. 2009 Jan 2;323(5910):133-8. doi: 10.1126/science.1162986. Epub 2008 Nov 20.
We present single-molecule, real-time sequencing data obtained from a DNA polymerase performing uninterrupted template-directed synthesis using four distinguishable fluorescently labeled deoxyribonucleoside triphosphates (dNTPs). We detected the temporal order of their enzymatic incorporation into a growing DNA strand with zero-mode waveguide nanostructure arrays, which provide optical observation volume confinement and enable parallel, simultaneous detection of thousands of single-molecule sequencing reactions. Conjugation of fluorophores to the terminal phosphate moiety of the dNTPs allows continuous observation of DNA synthesis over thousands of bases without steric hindrance. The data report directly on polymerase dynamics, revealing distinct polymerization states and pause sites corresponding to DNA secondary structure. Sequence data were aligned with the known reference sequence to assay biophysical parameters of polymerization for each template position. Consensus sequences were generated from the single-molecule reads at 15-fold coverage, showing a median accuracy of 99.3%, with no systematic error beyond fluorophore-dependent error rates.
我们展示了通过DNA聚合酶使用四种可区分的荧光标记脱氧核糖核苷三磷酸(dNTP)进行不间断模板导向合成而获得的单分子实时测序数据。我们利用零模式波导纳米结构阵列检测了它们酶促掺入生长中的DNA链的时间顺序,该阵列提供光学观察体积限制,并能够并行、同时检测数千个单分子测序反应。将荧光团与dNTP的末端磷酸基团共轭,使得能够在不受空间位阻的情况下对数千个碱基的DNA合成进行连续观察。这些数据直接报告了聚合酶动力学,揭示了与DNA二级结构相对应的不同聚合状态和暂停位点。将序列数据与已知参考序列比对,以测定每个模板位置的聚合生物物理参数。从覆盖度为15倍的单分子读数生成了一致序列,显示中位数准确率为99.3%,除了与荧光团相关的错误率外没有系统误差。