Kim Kyoohyun, Biswas Abin, Guck Jochen, Reber Simone
Max Planck Institute for the Science of Light, Erlangen, Germany.
Max-Planck-Zentrum für Physik und Medizin, Erlangen, Germany.
Methods Mol Biol. 2025;2958:119-141. doi: 10.1007/978-1-0716-4714-1_8.
Biological systems intricately regulate their density and volume throughout their life cycles and in response to physiological changes. Mass density, as a fundamental physical quantity, plays significant roles in biological processes such as differentiation, cell growth, protein synthesis, and condensate formation. Loss of density homeostasis on the other hand can have severe consequences including cellular senescence and disease states. Recent developments in biophotonics now enable high-resolution density quantification, providing new insights into the biophysical properties of cells and subcellular structures. One such technique is optical diffraction tomography (ODT), which offers label-free, high-resolution measurements of mass density distribution based on refractive index (RI) measurements. In this chapter, we present a comprehensive guide to implementing ODT for quantitative characterization of mass density distribution in biological systems, including in vivo (adherent cell culture) and in vitro (Xenopus egg extract) samples. We begin by detailing the optical setups, emphasizing key considerations for optimizing tomography acquisition. Subsequently, we introduce preparation protocols tailored to biological samples in various types of sample carriers and offer guidance on standard image acquisition and data analysis procedures. Finally, we address the challenges posed by the linear relationship between RI and mass density in complex substances, offering strategies for overcoming these limitations.
生物系统在其整个生命周期中以及对生理变化的响应过程中,会对其密度和体积进行复杂的调节。质量密度作为一个基本物理量,在诸如分化、细胞生长、蛋白质合成和凝聚物形成等生物过程中发挥着重要作用。另一方面,密度稳态的丧失可能会产生严重后果,包括细胞衰老和疾病状态。生物光子学的最新进展现在能够实现高分辨率的密度定量分析,为细胞和亚细胞结构的生物物理特性提供了新的见解。一种这样的技术是光学衍射层析成像(ODT),它基于折射率(RI)测量提供无标记的质量密度分布高分辨率测量。在本章中,我们提供了一份全面指南,介绍如何实施ODT以对生物系统中的质量密度分布进行定量表征,包括体内(贴壁细胞培养)和体外(非洲爪蟾卵提取物)样本。我们首先详细介绍光学设置,强调优化层析成像采集的关键注意事项。随后,我们介绍针对各种类型样本载体中的生物样本量身定制的制备方案,并提供标准图像采集和数据分析程序的指导。最后,我们解决复杂物质中RI与质量密度之间的线性关系所带来的挑战,提供克服这些限制的策略。