Korlach Jonas, Bjornson Keith P, Chaudhuri Bidhan P, Cicero Ronald L, Flusberg Benjamin A, Gray Jeremy J, Holden David, Saxena Ravi, Wegener Jeffrey, Turner Stephen W
Pacific Biosciences, Menlo Park, California, USA.
Methods Enzymol. 2010;472:431-55. doi: 10.1016/S0076-6879(10)72001-2.
Pacific Biosciences has developed a method for real-time sequencing of single DNA molecules (Eid et al., 2009), with intrinsic sequencing rates of several bases per second and read lengths into the kilobase range. Conceptually, this sequencing approach is based on eavesdropping on the activity of DNA polymerase carrying out template-directed DNA polymerization. Performed in a highly parallel operational mode, sequential base additions catalyzed by each polymerase are detected with terminal phosphate-linked, fluorescence-labeled nucleotides. This chapter will first outline the principle of this single-molecule, real-time (SMRT) DNA sequencing method, followed by descriptions of its underlying components and typical sequencing run conditions. Two examples are provided which illustrate that, in addition to the DNA sequence, the dynamics of DNA polymerization from each enzyme molecules is directly accessible: the determination of base-specific kinetic parameters from single-molecule sequencing reads, and the characterization of DNA synthesis rate heterogeneities.
太平洋生物科学公司开发了一种单DNA分子实时测序方法(Eid等人,2009年),其内在测序速度为每秒几个碱基,读长可达千碱基范围。从概念上讲,这种测序方法基于对进行模板导向DNA聚合的DNA聚合酶活性的监听。在高度并行的操作模式下,每个聚合酶催化的连续碱基添加通过末端磷酸连接的荧光标记核苷酸进行检测。本章将首先概述这种单分子实时(SMRT)DNA测序方法的原理,然后描述其基础组件和典型的测序运行条件。提供了两个例子,说明除了DNA序列外,还可以直接获取每个酶分子DNA聚合的动力学信息:从单分子测序读数中确定碱基特异性动力学参数,以及表征DNA合成速率的异质性。