Department of Biochemistry and Cell Biology, Rice University, Houston, Texas.
Biophys J. 2010 Aug 4;99(3):887-96. doi: 10.1016/j.bpj.2010.04.076.
Success in evolution depends critically upon the ability of organisms to adapt, a property that is also true for the proteins that contribute to the fitness of an organism. Successful protein evolution is enhanced by mutational pathways that generate a wide range of physicochemical mechanisms to adaptation. In an earlier study, we used a weak-link method to favor changes to an essential but maladapted protein, adenylate kinase (AK), within a microbial population. Six AK mutants (a single mutant followed by five double mutants) had success within the population, revealing a diverse range of adaptive strategies that included changes in nonpolar packing, protein folding dynamics, and formation of new hydrogen bonds and electrostatic networks. The first mutation, AK(BSUB) Q199R, was essential in defining the structural context that facilitated subsequent mutations as revealed by a considerable mutational epistasis and, in one case, a very strong dependence upon the order of mutations. Namely, whereas the single mutation AK(BSUB) G213E decreases protein stability by >25 degrees C, the same mutation in the background of AK(BSUB) Q199R increases stability by 3.4 degrees C, demonstrating that the order of mutations can play a critical role in favoring particular molecular pathways to adaptation. In turn, protein folding kinetics shows that four of the five AK(BSUB) double mutants utilize a strategy in which an increase in the folding rate accompanied by a decrease in the unfolding rate results in additional stability. However, one mutant exhibited a dramatic increase in the folding relative to a modest increase in the unfolding rate, suggesting a different adaptive strategy for thermostability. In all cases, an increase in the folding rates for the double mutants appears to be the preferred mechanism in conferring additional stability and may be an important aspect of protein evolution. The range of overlapping as well as contrasting strategies for success illustrates both the power and subtlety of adaptation at even the smallest unit of change, a single amino acid.
进化的成功取决于生物体适应的能力,这一特性也适用于有助于生物体适应性的蛋白质。通过产生广泛的物理化学机制来适应的突变途径,可以增强成功的蛋白质进化。在早期的一项研究中,我们使用弱键方法来促进微生物种群中关键但不适应的蛋白(腺苷酸激酶(AK))的变化。六种 AK 突变体(一个单点突变后是五个双点突变)在种群中取得了成功,揭示了一系列不同的适应策略,包括非极性包装、蛋白质折叠动力学以及新氢键和静电网络的形成的变化。第一个突变 AK(BSUB) Q199R 在定义结构环境方面是必不可少的,该结构环境促进了随后的突变,这表现出相当大的突变上位性,在一种情况下,对突变顺序有很强的依赖性。即,虽然单点突变 AK(BSUB) G213E 使蛋白质稳定性降低超过 25°C,但在 AK(BSUB) Q199R 的背景下相同的突变使稳定性增加 3.4°C,这表明突变的顺序可以在有利于特定分子适应途径方面发挥关键作用。反过来,蛋白质折叠动力学表明,五个 AK(BSUB) 双突变体中的四个利用了一种策略,其中折叠速率的增加伴随着解折叠速率的降低,导致额外的稳定性。然而,一个突变体表现出相对于解折叠速率适度增加的折叠相对显著增加,表明了热稳定性的不同适应策略。在所有情况下,双突变体的折叠速率增加似乎是赋予额外稳定性的首选机制,这可能是蛋白质进化的一个重要方面。重叠和对比策略的范围都说明了即使是最小的变化单位,即单个氨基酸,适应的力量和微妙之处。