力谱学
分子动力学
圆二色性
材料科学
疏水效应
捆绑
分子
限制
螺旋(腹足类)
氢键
化学物理
结晶学
螺旋束
生物分子
纳米技术
化学
蛋白质结构
原子力显微镜
计算化学
复合材料
工程类
蜗牛
有机化学
生物
机械工程
生物化学
生态学
作者
Yifan Meng,Guo-Jin Tang,Ruhai Wang,Bin Zheng,Yuanhao Liu,Hantian Zhang,Peng Zheng
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-10-21
卷期号:19 (43): 38077-38085
被引量:1
标识
DOI:10.1021/acsnano.5c13783
摘要
α-Helical domains are widespread and versatile, yet typically fail under low mechanical load because backbone hydrogen bonds unzip sequentially, limiting their use in force-bearing nanomaterials and molecular devices. We present an AI-guided strategy to design six-helix bundle proteins with densely packed hydrophobic cores that co-optimize mechanical and thermal stability. Backbones were generated with RFdiffusion, sequences designed with ProteinMPNN, and structures validated by AlphaFold2/ESMFold; steered and annealing molecular dynamics simulation identified designs with high predicted unfolding forces and heat resilience. Three selected constructs (HP149, HP206, HP347) expressed solubly and folded as predominantly α-helical by circular dichroism. AFM-based single-molecule force spectroscopy revealed unfolding forces approaching 100 pN, much higher than typical α-helical domains (∼20 pN). All three retained substantial helical content to ≥100 °C. Mutating buried hydrophobic residues (V17S, L104R in HP149) reduced unfolding forces, confirming core packing as an important determinant. These results establish hydrophobic-core design as a promising route to robust α-helical scaffolds.
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