用于微流体捕获和单细胞TIRF成像的芯片上实验室装置

IF 3 4区 医学 Q3 ENGINEERING, BIOMEDICAL
Dustin Dzikonski, Riccardo Zamboni, Aniket Bandyopadhyay, Deepthi Paul, Roland Wedlich-Söldner, Cornelia Denz, Jörg Imbrock
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引用次数: 0

摘要

全内反射荧光(TIRF)显微镜是一种强大的成像技术,可以可视化靠近底物的标本外表面,从而对细胞膜组成产生重要的见解。TIRF在单细胞研究中起着关键作用,但通常需要化学固定来确保细胞膜和底物之间的直接接触,这可能会损害细胞活力并促进聚集。在这项研究中,我们提出了一种微流控装置,其结构设计用于捕获单个酵母细胞并将其固定在与底物表面直接接触的位置,以便在细胞膜上进行TIRF测量。陷阱是用双光子聚合制造的,允许高分辨率打印复杂的结构,在所有三个维度上封装细胞,同时保持暴露在设备内的流动中。我们的适应性陷阱设计使我们能够减少被困细胞的残余运动到最低限度,同时保持高的陷阱效率。我们确定了捕获单个酵母细胞的最佳结构配置,并证明捕获效率可以通过修改细胞浓度和注射方法来调整。此外,通过用软水凝胶材料复制细胞陷阱设计,我们证明了我们的方法在进一步的单细胞研究中的潜力。作者没有相关的财务或非经济利益需要披露,也没有竞争利益需要申报。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lab-on-a-chip device for microfluidic trapping and TIRF imaging of single cells

Total internal reflection fluorescence (TIRF) microscopy is a powerful imaging technique that visualizes the outer surface of specimens in close proximity to a substrate, yielding crucial insights in cell membrane compositions. TIRF plays a key role in single-cell studies but typically requires chemical fixation to ensure direct contact between the cell membrane and substrate, which can compromise cell viability and promote clustering. In this study, we present a microfluidic device with structures designed to trap single yeast cells and fix them in direct contact with the substrate surface to enable TIRF measurements on the cell membrane. The traps are fabricated using two-photon polymerization, allowing high-resolution printing of intricate structures that encapsulate cells in all three dimensions while maintaining exposure to the flow within the device. Our adaptable trap design allows us to reduce residual movement of trapped cells to a minimum while maintaining high trapping efficiencies. We identify the optimal structure configuration to trap single yeast cells and demonstrate that trapping efficiency can be tuned by modifying cell concentration and injection methods. Additionally, by replicating the cell trap design with soft hydrogel materials, we demonstrate the potential of our approach for further single-cell studies. The authors have no relevant financial or non-financial interests to disclose and no competing interests to declare.

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来源期刊
Biomedical Microdevices
Biomedical Microdevices 工程技术-工程:生物医学
CiteScore
6.90
自引率
3.60%
发文量
32
审稿时长
6 months
期刊介绍: Biomedical Microdevices: BioMEMS and Biomedical Nanotechnology is an interdisciplinary periodical devoted to all aspects of research in the medical diagnostic and therapeutic applications of Micro-Electro-Mechanical Systems (BioMEMS) and nanotechnology for medicine and biology. General subjects of interest include the design, characterization, testing, modeling and clinical validation of microfabricated systems, and their integration on-chip and in larger functional units. The specific interests of the Journal include systems for neural stimulation and recording, bioseparation technologies such as nanofilters and electrophoretic equipment, miniaturized analytic and DNA identification systems, biosensors, and micro/nanotechnologies for cell and tissue research, tissue engineering, cell transplantation, and the controlled release of drugs and biological molecules. Contributions reporting on fundamental and applied investigations of the material science, biochemistry, and physics of biomedical microdevices and nanotechnology are encouraged. A non-exhaustive list of fields of interest includes: nanoparticle synthesis, characterization, and validation of therapeutic or imaging efficacy in animal models; biocompatibility; biochemical modification of microfabricated devices, with reference to non-specific protein adsorption, and the active immobilization and patterning of proteins on micro/nanofabricated surfaces; the dynamics of fluids in micro-and-nano-fabricated channels; the electromechanical and structural response of micro/nanofabricated systems; the interactions of microdevices with cells and tissues, including biocompatibility and biodegradation studies; variations in the characteristics of the systems as a function of the micro/nanofabrication parameters.
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