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Mapping mechanical properties of living cells at nanoscale using intrinsic nanopipette-sample force interactions dagger

机译:映射活细胞的力学性能纳米级使用内在nanopipette-sample力交互匕首

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摘要

Mechanical properties of living cells determined by cytoskeletal elements play a crucial role in a wide range of biological functions. However, low-stress mapping of mechanical properties with nanoscale resolution but with a minimal effect on the fragile structure of cells remains difficult. Scanning Ion-Conductance Microscopy (SICM) for quantitative nanomechanical mapping (QNM) is based on intrinsic force interactions between nanopipettes and samples and has been previously suggested as a promising alternative to conventional techniques. In this work, we have provided an alternative estimation of intrinsic force and stress and demonstrated the possibility to perform qualitative and quantitative analysis of cell nanomechanical properties of a variety of living cells. Force estimation on decane droplets with well-known elastic properties, similar to living cells, revealed that the forces applied using a nanopipette are much smaller than in the case using atomic force microscopy. We have shown that we can perform nanoscale topography and QNM using a scanning procedure with no detectable effect on live cells, allowing long-term QNM as well as detection of nanomechanical properties under drug-induced alterations of actin filaments and microtubulin.
机译:活细胞的力学性能决定通过细胞骨架元素发挥着至关重要的作用广泛的生物功能。压力小的映射的机械性能纳米级分辨率,但影响很小脆弱的细胞结构仍然是困难的。Ion-Conductance扫描显微镜(SICM)定量纳米机械映射(QNM)基于内在力量之间的相互作用nanopipettes和样品之前建议作为一个有前途的替代传统的技术。提供另一种内在的估计力和压力,并演示了这种可能性进行定性和定量分析细胞的纳米机械的各种属性活细胞。与著名的弹性性质,类似活细胞,显示力量使用nanopipette比在小得多使用原子力显微镜。我们可以执行纳米地形和QNM使用扫描过程,没有检测到影响活细胞,使长期QNM检测的纳米机械属性在药物引起的肌动蛋白丝的改变和microtubulin。

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