Beausang John F, Nelson Philip C
Department of Physics and Astronomy, University of Pennsylvania, Philadelphia, PA 19104, USA.
Phys Biol. 2007 Oct 9;4(3):205-19. doi: 10.1088/1478-3975/4/3/007.
In many biochemical processes, proteins bound to DNA at distant sites are brought into close proximity by loops in the underlying DNA. For example, the function of some gene-regulatory proteins depends on such 'DNA looping' interactions. We present a new technique for characterizing the kinetics of loop formation in vitro, as observed using the tethered particle method, and apply it to experimental data on looping induced by lambda repressor. Our method uses a modified ('diffusive') hidden Markov analysis that directly incorporates the Brownian motion of the observed tethered bead. We compare looping lifetimes found with our method (which we find are consistent over a range of sampling frequencies) to those obtained via the traditional threshold-crossing analysis (which can vary depending on how the raw data are filtered in the time domain). Our method does not involve any time filtering and can detect sudden changes in looping behavior. For example, we show how our method can identify transitions between long-lived, kinetically distinct states that would otherwise be difficult to discern.
在许多生化过程中,与远处DNA位点结合的蛋白质通过其下方DNA的环化而彼此靠近。例如,一些基因调控蛋白的功能就依赖于这种“DNA环化”相互作用。我们提出了一种新的技术,用于在体外表征环化形成的动力学,该技术采用系留粒子法进行观测,并将其应用于λ阻遏物诱导环化的实验数据。我们的方法使用了一种改进的(“扩散性”)隐马尔可夫分析,该分析直接纳入了观测到的系留珠子的布朗运动。我们将用我们的方法得到的环化寿命(我们发现在一系列采样频率下是一致的)与通过传统的阈值交叉分析得到的环化寿命进行比较(后者可能因在时域中对原始数据的滤波方式而异)。我们的方法不涉及任何时间滤波,并且可以检测环化行为的突然变化。例如,我们展示了我们的方法如何识别寿命长、动力学性质不同的状态之间的转变,而这些转变在其他情况下很难辨别。