光学镊子
折叠(DSP实现)
原子力显微镜
纳米技术
磁镊
镊子
DNA
材料科学
荧光团
力谱学
化学
光学力
生物物理学
A-DNA
分子动力学
显微镜
可视化
生物系统
荧光
刚度(电磁)
动力学(音乐)
离解(化学)
持续时间
分子生物物理学
弹性(物理)
粘弹性
作者
Kenichi Umeda,Shin’nosuke Yamanaka,Motonori Imamura,Fritz Nagae,Shingo Fukuda,Hiroki Watanabe,Takayuki Uchihashi,Shoji Takada,Toshio Ando
标识
DOI:10.1021/acs.jpclett.5c03517
摘要
Optical tweezers have contributed to elucidating the folding mechanisms associated with biomolecules. By combining them with fluorescence imaging techniques, imaging can also be performed while measuring or applying forces that couple to biochemical reactions; however, they cannot capture structural information beyond the fluorophore spatial resolution. To overcome this limitation, here, we developed a hybrid high-speed atomic force microscopy (HS-AFM) and optical tweezers system. To resolve the challenge of incompatible instrumental configurations, we designed a customized optical tweezers system optimized for HS-AFM. Using this platform, we applied external forces to synthetic DNA secondary structures and directly visualized duplex dissociation and spontaneous reannealing upon force release, demonstrating reversible control of folding. We also captured reversible DNA overstretching and transient secondary structure formation in ssDNA. These findings were further analyzed using molecular dynamics simulations and viscoelastic modeling. This integrated approach provides a powerful platform for investigating folding dynamics and force-coupled mechanisms in biomolecules.
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