力谱学
分子动力学
材料科学
疏水效应
捆绑
分子
限制
氢键
化学物理
结晶学
同种类的
生物分子
纳米技术
纳米材料
芯(光纤)
退火(玻璃)
蛋白质设计
热的
化学
光谱学
工作(物理)
分子构象
蛋白质结构
晶格蛋白
设计要素和原则
材料设计
蛋白质折叠
力场(虚构)
自组装
模拟退火
生物物理学
生物系统
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI