Department of Chemistry & Biochemistry, Kent State University.
Department of Chemistry & Biochemistry, Kent State University;
J Vis Exp. 2022 Jul 26(185). doi: 10.3791/63741.
Single-molecule techniques based on fluorescence and mechanochemical principles provide superior sensitivity in biological sensing. However, due to the lack of high throughput capabilities, the application of these techniques is limited in biophysics. Ensemble force spectroscopy (EFS) has demonstrated high throughput in the investigation of a massive set of molecular structures by converting mechanochemical studies of individual molecules into those of molecular ensembles. In this protocol, the DNA secondary structures (i-motifs) were unfolded in the shear flow between the rotor and stator of a homogenizer tip at shear rates up to 77796/s. The effects of flow rates and molecular sizes on the shear forces experienced by the i-motif were demonstrated. The EFS technique also revealed the binding affinity between DNA i-motifs and ligands. Furthermore, we have demonstrated a click chemistry reaction that can be actuated by shear force (i.e., mechano-click chemistry). These results establish the effectiveness of using shear force to control the conformation of molecular structures.
基于荧光和机械化学原理的单分子技术在生物传感中提供了卓越的灵敏度。然而,由于缺乏高通量能力,这些技术在生物物理学中的应用受到限制。整体力谱学(EFS)通过将单个分子的机械化学研究转化为分子集合体的研究,在大规模分子结构的研究中展示了高通量能力。在本方案中,在匀浆器尖端的转子和定子之间的剪切流中,将 DNA 二级结构(i-motif)在剪切速率高达 77796/s 下展开。证明了流速和分子大小对 i-motif 所受剪切力的影响。EFS 技术还揭示了 DNA i-motif 与配体之间的结合亲和力。此外,我们还证明了可以通过剪切力(即机械点击化学)引发点击化学反应。这些结果确立了使用剪切力控制分子结构构象的有效性。