Wickstrom Lauren, Bi Yuan, Hornak Viktor, Raleigh Daniel P, Simmerling Carlos
Biochemistry and Structural Biology Program, State University of New York, Stony Brook, New York 11794-3400, USA.
Biochemistry. 2007 Mar 27;46(12):3624-34. doi: 10.1021/bi061785+. Epub 2007 Mar 6.
The 36-residue helical subdomain of the villin headpiece, HP36, is one of the smallest cooperatively folded proteins, folding on the microsecond time scale. The domain is an extraordinarily popular model system for both experimental and computational studies of protein folding. The structure of HP36 has been determined using X-ray crystallography and NMR spectroscopy, with the resulting structures exhibiting differences in helix packing, van der Waals contacts, and hydrogen bonding. It is important to determine the solution structure of HP36 with as much accuracy as possible since this structure is widely used as a reference for simulations and experiments. We complement the existing data by using all-atom molecular dynamics simulations with explicit solvent to evaluate which of the experimental models is the better representation of HP36 in solution. After simulation for 50 ns initiated with the NMR structure, we observed that the protein spontaneously adopts structures with a backbone conformation, core packing, and C-capping motif on the third helix that are more consistent with the crystal structure. We also examined hydrogen bonding and side chain packing interactions between D44 and R55 and between F47 and R55, respectively, which were observed in the crystal structure but not in the NMR-based solution structure. Simulations showed large fluctuations in the distance between D44 and R55, while the distance between F47 and R55 remained stable, suggesting the formation of a cation-pi interaction between those residues. Experimental double mutant cycles confirmed that the F47-R55 pair has a larger energetic coupling than the D44-R55 interaction. Overall, these combined experimental and computational studies show that the X-ray crystal structure is the better reference structure for HP36 in solution at neutral pH. Our analysis also shows how detailed molecular dynamics simulations combined with experimental validation can help bridge the gap between NMR and crystallographic methods.
绒毛蛋白头部结构域的36个残基螺旋亚结构域HP36是最小的协同折叠蛋白之一,其折叠发生在微秒时间尺度上。该结构域是蛋白质折叠实验研究和计算研究中极为常用的模型系统。HP36的结构已通过X射线晶体学和核磁共振光谱法确定,所得结构在螺旋堆积、范德华接触和氢键方面存在差异。尽可能精确地确定HP36的溶液结构非常重要,因为该结构被广泛用作模拟和实验的参考。我们通过使用含明确溶剂的全原子分子动力学模拟来补充现有数据,以评估哪种实验模型能更好地代表溶液中的HP36。在用核磁共振结构启动50纳秒的模拟后,我们观察到该蛋白质自发地采用了一种主链构象、核心堆积以及第三螺旋上的C端帽基序与晶体结构更一致的结构。我们还分别研究了晶体结构中但基于核磁共振的溶液结构中未观察到的D44与R55之间以及F47与R55之间的氢键和侧链堆积相互作用。模拟显示D44与R55之间的距离有很大波动,而F47与R55之间的距离保持稳定,这表明这些残基之间形成了阳离子-π相互作用。实验性双突变循环证实F47-R55对的能量耦合比D44-R55相互作用更大。总体而言,这些结合的实验和计算研究表明,在中性pH条件下,X射线晶体结构是溶液中HP36更好的参考结构。我们的分析还展示了详细的分子动力学模拟与实验验证相结合如何有助于弥合核磁共振和晶体学方法之间的差距。