Department of Physics, University of Michigan, Ann Arbor, Michigan.
Debye Institute, Molecular Biophysics, Utrecht University, Utrecht, The Netherlands.
Biophys J. 2014 Feb 4;106(3):705-15. doi: 10.1016/j.bpj.2013.12.024.
The lac repressor protein (LacI) efficiently represses transcription of the lac operon in Escherichia coli by binding to two distant operator sites on the bacterial DNA and causing the intervening DNA to form a loop. We employed single-molecule tethered particle motion to observe LacI-mediated loop formation and breakdown in DNA constructs that incorporate optimized operator binding sites and intrinsic curvature favorable to loop formation. Previous bulk competition assays indirectly measured the loop lifetimes in these optimized DNA constructs as being on the order of days; however, we measured these same lifetimes to be on the order of minutes for both looped and unlooped states. In a range of single-molecule DNA competition experiments, we found that the resistance of the LacI-DNA complex to competitive binding is a function of both the operator strength and the interoperator sequence. To explain these findings, we present what we believe to be a new kinetic model of loop formation and DNA competition. In this proposed new model, we hypothesize a new unlooped state in which the unbound DNA-binding domain of the LacI protein interacts nonspecifically with nonoperator DNA adjacent to the operator site at which the second LacI DNA-binding domain is bound.
阻遏蛋白(LacI)通过与细菌 DNA 上两个遥远的操纵子结合,使中间的 DNA 形成环,从而有效地抑制 lac 操纵子的转录。我们采用单分子系绳粒子运动来观察在包含优化的操纵子结合位点和有利于环形成的固有曲率的 DNA 构建体中 LacI 介导的环形成和分解。先前的批量竞争测定法间接测量了这些优化的 DNA 构建体中环的寿命约为几天;然而,我们测量到环和未环状态的相同寿命约为几分钟。在一系列单分子 DNA 竞争实验中,我们发现 LacI-DNA 复合物对竞争结合的抵抗力是操纵子强度和操纵子间序列的函数。为了解释这些发现,我们提出了一个我们认为是环形成和 DNA 竞争的新动力学模型。在这个提出的新模型中,我们假设了一种新的未环状态,其中未结合的 LacI 蛋白的 DNA 结合域与结合在第二个 LacI DNA 结合域的操纵子相邻的非操纵子 DNA 非特异性相互作用。