Hyeon Changbong, Thirumalai D
Biophysics Program, Institute for Physical Science and Technology, Department of Chemistry and Biochemistry, University of Maryland, College Park, Maryland, USA.
Biophys J. 2007 Feb 1;92(3):731-43. doi: 10.1529/biophysj.106.093062. Epub 2006 Oct 6.
Mechanical unfolding of RNA structures, ranging from hairpins to ribozymes, using laser optical tweezer experiments have begun to reveal the features of the energy landscape that cannot be easily explored using conventional experiments. Upon application of constant force (f), RNA hairpins undergo cooperative transitions from folded to unfolded states whereas subdomains of ribozymes unravel one at a time. Here, we use a self-organized polymer model and Brownian dynamics simulations to probe mechanical unfolding at constant force and constant-loading rate of four RNA structures of varying complexity. For simple hairpins, such as P5GA, application of constant force or constant loading rate results in bistable cooperative transitions between folded and unfolded states without populating any intermediates. The transition state location (DeltaxFTS) changes dramatically as the loading rate is varied. At loading rates comparable to those used in laser optical tweezer experiments, the hairpin is plastic, with DeltaxFTS being midway between folded and unfolded states; whereas at high loading rates, DeltaxFTS moves close to the folded state, i.e., RNA is brittle. For the 29-nucleotide TAR RNA with the three-nucleotide bulge, unfolding occurs in a nearly two-state manner with an occasional pause in a high free energy metastable state. Forced unfolding of the 55 nucleotides of the Hepatitis IRES domain IIa, which has a distorted L-shaped structure, results in well-populated stable intermediates. The most stable force-stabilized intermediate represents straightening of the L-shaped structure. For these structures, the unfolding pathways can be predicted using the contact map of the native structures. Unfolding of a RNA motif with internal multiloop, namely, the 109-nucleotide prohead RNA that is part of the 29 DNA packaging motor, at constant value of rf occurs with three distinct rips that represent unraveling of the paired helices. The rips represent kinetic barriers to unfolding. Our work shows 1), the response of RNA to force is largely determined by the native structure; and 2), only by probing mechanical unfolding over a wide range of forces can the underlying energy landscape be fully explored.
利用激光光镊实验对从发夹结构到核酶的RNA结构进行机械展开,已开始揭示传统实验难以探索的能量景观特征。在施加恒定力(f)时,RNA发夹会经历从折叠态到展开态的协同转变,而核酶的亚结构域则一次解开一个。在这里,我们使用自组织聚合物模型和布朗动力学模拟来探究在恒定力和恒定加载速率下四种不同复杂程度的RNA结构的机械展开。对于简单的发夹结构,如P5GA,施加恒定力或恒定加载速率会导致折叠态和展开态之间的双稳态协同转变,不会出现任何中间体。随着加载速率的变化,过渡态位置(ΔxFTS)会发生显著变化。在与激光光镊实验中使用的加载速率相当的情况下,发夹是可塑的,ΔxFTS位于折叠态和展开态之间的中间位置;而在高加载速率下,ΔxFTS会靠近折叠态移动,即RNA是脆性的。对于具有三核苷酸凸起的29个核苷酸的TAR RNA,展开以近乎两态的方式发生,偶尔会在高自由能亚稳态中暂停。对具有扭曲L形结构的丙型肝炎IRES结构域IIa的55个核苷酸进行强制展开,会产生大量稳定的中间体。最稳定的力稳定中间体代表L形结构的伸直。对于这些结构,可以使用天然结构的接触图来预测展开途径。在恒定的rf值下,对具有内部多环的RNA基序(即作为29 DNA包装马达一部分的109个核苷酸的原头部RNA)进行展开时,会出现三个不同的撕裂,代表配对螺旋的解开。这些撕裂代表展开的动力学障碍。我们的工作表明:1)RNA对力的响应在很大程度上由天然结构决定;2)只有在广泛的力范围内探究机械展开,才能充分探索潜在的能量景观。