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使用抗体功能化纳米针和原子力显微镜评估肌动蛋白细胞骨架状态。

Evaluation of the actin cytoskeleton state using an antibody-functionalized nanoneedle and an AFM.

机构信息

Biomedical Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Central 4, 1-1-1 Higashi, Tsukuba, Ibaraki 305-8562, Japan.

出版信息

Biosens Bioelectron. 2013 Feb 15;40(1):3-9. doi: 10.1016/j.bios.2012.06.044. Epub 2012 Jun 29.

Abstract

A cell diagnosis technique was developed, which uses an Atomic Force Microscope (AFM) and an ultra-thin AFM probe sharpened to a diameter of 200 nm (nanoneedle). Due to the high aspect ratio of the nanoneedle, it was successfully inserted into a living cell without affecting its viability. Furthermore, by functionalizing the nanoneedle with specific antibodies and measuring the unbinding forces ('fishing forces') during evacuation of the nanoneedle from the cell, it was possible to measure specific mechanical interactions between the antibody-functionalized nanoneedle and the intracellular contents of the cell. In this study, an anti-actin-antibody-functionalized nanoneedle was used to evaluate the actin cytoskeleton state in living cells. To examine the effect of cytoskeleton condition on the measured fishing forces, the cytoskeleton-disrupting drugs cytochalasin D (cytD) and Y-27632 were used, showing a marked decrease in the measured fishing forces following incubation with either of the drugs. Furthermore, the technique was used to measure the time course changes in a single cell during incubation with cytD, showing a gradual time-dependent decrease in fishing forces. Even minute doses of the drugs, the effects of which were hardly evident by optical and fluorescence methods, could be clearly detected by the measurement of nanoneedle-protein fishing forces, pointing to the high sensitivity of this detection method. This technique may prove beneficial for the evaluation of cytoskeleton conditions in health and disease, and for the selection of specific cells according to their intracellular protein contents, without the need for introduction of marker proteins into the cell.

摘要

开发了一种细胞诊断技术,该技术使用原子力显微镜 (AFM) 和直径为 200nm(纳米针)的超锋利 AFM 探针。由于纳米针的高纵横比,它成功地插入活细胞而不影响其活力。此外,通过将纳米针功能化特定的抗体,并测量从细胞中抽出纳米针时的非结合力(“钓鱼力”),可以测量抗体功能化纳米针与细胞内内容物之间的特定机械相互作用。在这项研究中,使用抗肌动蛋白抗体功能化的纳米针来评估活细胞中的肌动蛋白细胞骨架状态。为了研究细胞骨架状态对测量钓鱼力的影响,使用了细胞骨架破坏药物细胞松弛素 D (cytD) 和 Y-27632,孵育后测量到的钓鱼力明显下降。此外,该技术还用于测量单个细胞在孵育 cytD 过程中的时间过程变化,显示钓鱼力逐渐随时间下降。即使是药物的微小剂量,光学和荧光方法几乎无法检测到其作用,但通过测量纳米针-蛋白钓鱼力可以清楚地检测到,表明这种检测方法具有很高的灵敏度。该技术可能有助于评估健康和疾病中的细胞骨架状态,并根据细胞内蛋白质含量选择特定的细胞,而无需向细胞中引入标记蛋白。

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