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Multimodal interference-based imaging of nanoscale structure and macromolecular motion uncovers UV induced cellular paroxysm

机译:基于多峰干涉的纳米级结构和大分子运动成像揭示了紫外线诱发的细胞阵发性

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摘要

Understanding the relationship between intracellular motion and macromolecular structure remains a challenge in biology. Macromolecular structures are assembled from numerous molecules, some of which cannot be labeled. Most techniques to study motion require potentially cytotoxic dyes or transfection, which can alter cellular behavior and are susceptible to photobleaching. Here we present a multimodal label-free imaging platform for measuring intracellular structure and macromolecular dynamics in living cells with a sensitivity to macromolecular structure as small as 20 nm and millisecond temporal resolution. We develop and validate a theory for temporal measurements of light interference. In vitro, we study how higher-order chromatin structure and dynamics change during cell differentiation and ultraviolet (UV) light irradiation. Finally, we discover cellular paroxysms, a near-instantaneous burst of macromolecular motion that occurs during UV induced cell death. With nanoscale sensitive, millisecond resolved capabilities, this platform could address critical questions about macromolecular behavior in live cells.
机译:了解细胞内运动与大分子结构之间的关系仍然是生物学中的挑战。大分子结构是由许多分子组装而成的,其中一些无法标记。大多数研究运动的技术都需要潜在的细胞毒性染料或转染,这会改变细胞行为并容易发生光漂白。在这里,我们提出了一种多模式无标记成像平台,用于测量活细胞中的细胞内结构和大分子动力学,对小至20 nm的大分子结构和毫秒级的时间分辨率敏感。我们开发并验证了用于光干扰的时间测量的理论。在体外,我们研究了细胞分化和紫外线(UV)照射期间高级染色质结构和动力学如何变化。最后,我们发现细胞阵发性发作,这是在紫外线诱导的细胞死亡过程中发生的近乎瞬时的大分子运动爆发。借助纳米级敏感的毫秒级解析功能,该平台可以解决有关活细胞中大分子行为的关键问题。

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