Faísca P F N, Travasso R D M, Ball R C, Shakhnovich E I
Centro de Fisica Teorica e Computacional, Universidade de Lisboa, Av. Prof. Gama Pinto 2, 1649-003 Lisboa, Portugal.
J Chem Phys. 2008 Sep 7;129(9):095108. doi: 10.1063/1.2973624.
We apply a simulational proxy of the phi-value analysis and perform extensive mutagenesis experiments to identify the nucleating residues in the folding "reactions" of two small lattice Go polymers with different native geometries. Our findings show that for the more complex native fold (i.e., the one that is rich in nonlocal, long-range bonds), mutation of the residues that form the folding nucleus leads to a considerably larger increase in the folding time than the corresponding mutations in the geometry that is predominantly local. These results are compared to data obtained from an accurate analysis based on the reaction coordinate folding probability P(fold) and on structural clustering methods. Our study reveals a complex picture of the transition state ensemble. For both protein models, the transition state ensemble is rather heterogeneous and splits up into structurally different populations. For the more complex geometry the identified subpopulations are actually structurally disjoint. For the less complex native geometry we found a broad transition state with microscopic heterogeneity. These findings suggest that the existence of multiple transition state structures may be linked to the geometric complexity of the native fold. For both geometries, the identification of the folding nucleus via the P(fold) analysis agrees with the identification of the folding nucleus carried out with the phi-value analysis. For the most complex geometry, however, the applied methodologies give more consistent results than for the more local geometry. The study of the transition state structure reveals that the nucleus residues are not necessarily fully native in the transition state. Indeed, it is only for the more complex geometry that two of the five critical residues show a considerably high probability of having all its native bonds formed in the transition state. Therefore, one concludes that, in general, the phi-value correlates with the acceleration/deceleration of folding induced by mutation, rather than with the degree of nativeness of the transition state, and that the "traditional" interpretation of phi-values may provide a more realistic picture of the structure of the transition state only for more complex native geometries.
我们应用phi值分析的模拟替代方法,并进行广泛的诱变实验,以确定两种具有不同天然几何结构的小晶格Go聚合物折叠“反应”中的成核残基。我们的研究结果表明,对于更复杂的天然折叠结构(即富含非局部、长程键的结构),形成折叠核的残基发生突变导致折叠时间的增加幅度,比主要为局部结构的几何结构中相应突变导致的增加幅度大得多。将这些结果与基于反应坐标折叠概率P(fold)和结构聚类方法的精确分析所获得的数据进行比较。我们的研究揭示了过渡态系综的复杂情况。对于这两种蛋白质模型,过渡态系综相当不均匀,并且分裂成结构不同的群体。对于更复杂的几何结构,所识别的亚群体实际上在结构上是不相连的。对于不太复杂的天然几何结构,我们发现了具有微观不均匀性的宽泛过渡态。这些发现表明,多个过渡态结构的存在可能与天然折叠的几何复杂性有关。对于这两种几何结构,通过P(fold)分析确定的折叠核与通过phi值分析确定的折叠核一致。然而,对于最复杂的几何结构,所应用的方法比对于更局部的几何结构给出的结果更一致。对过渡态结构的研究表明,核残基在过渡态中不一定完全是天然状态。实际上,只有对于更复杂的几何结构,五个关键残基中的两个在过渡态中形成所有天然键的概率相当高。因此,可以得出结论,一般来说,phi值与突变引起的折叠加速/减速相关,而不是与过渡态的天然程度相关,并且phi值的“传统”解释可能仅对于更复杂的天然几何结构才能提供更真实的过渡态结构情况。