Shen Nan, Datta Dabajyoti, Schaffer Chris B, LeDuc Philip, Ingber Donald E, Mazur Eric
Department of Physics, Harvard University, USA.
Mech Chem Biosyst. 2005;2(1):17-25.
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.
细胞调控分析需要能够在纳米尺度上对活细胞内分子过程进行空间分辨扰动的方法。我们提出了一种使用低重复率、低能量飞秒激光脉冲消融活细胞内分子结构的技术。通过将这些脉冲紧密聚焦在细胞膜下方,我们通过非线性过程消融细胞内的细胞物质。我们选择性地去除了细胞骨架和单个线粒体的亚微米区域,而不改变相邻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制进行非侵入性操作。使用这种方法,我们明确证明线粒体是结构独立的功能单元,并不像过去一些研究所表明的那样形成连续网络。