Ablation of cytoskeletal filaments and mitochondria in live cells using a femtosecond laser nanoscissor.

Nan Shen, Dabajyoti Datta, Chris B Schaffer, Philip LeDuc, Donald E Ingber, Eric Mazur
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Abstract

Analysis of cell regulation requires methods for perturbing molecular processes within living cells with spatial discrimination on the nanometer-scale. We present a technique for ablating molecular structures in living cells using low-repetition rate, low-energy femtosecond laser pulses. By tightly focusing these pulses beneath the cell membrane, we ablate cellular material inside the cell through nonlinear processes. We selectively removed sub-micrometer regions of the cytoskeleton and individual mitochondria without altering neighboring structures or compromising cell viability. This nanoscissor technique enables non-invasive manipulation of the structural machinery of living cells with several-hundred-nanometer resolution. Using this approach, we unequivocally demonstrate that mitochondria are structurally independent functional units, and do not form a continuous network as suggested by some past studies.

用飞秒激光纳米剪刀消融活细胞中的细胞骨架细丝和线粒体。
细胞调控的分析需要在纳米尺度上对活细胞内的分子过程进行空间分辨的扰动方法。我们提出了一种利用低重复率、低能量飞秒激光脉冲消融活细胞分子结构的技术。通过将这些脉冲紧密聚焦在细胞膜下,我们通过非线性过程烧蚀细胞内的细胞物质。我们选择性地去除细胞骨架和单个线粒体的亚微米区域,而不改变邻近结构或损害细胞活力。这种纳米剪刀技术能够以几百纳米的分辨率对活细胞的结构机械进行非侵入性操作。使用这种方法,我们明确地证明了线粒体是结构上独立的功能单位,并没有像过去的一些研究表明的那样形成连续的网络。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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