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植物根系中纳米颗粒的精确追踪

Precise tracking of nanoparticles in plant roots.

作者信息

Sun Xiao-Dong, Ma Jing-Ya, Feng Li-Juan, Duan Jian-Lu, Yuan Xian-Zheng

机构信息

Shandong Key Laboratory of Environmental Processes and Health, School of Environmental Science and Engineering, Shandong University, Qingdao, Shandong, P. R. China.

Sino-French Research Institute for Ecology and Environment (ISFREE), Shandong University, Qingdao, Shandong, P. R. China.

出版信息

Nat Protoc. 2025 Jan;20(1):248-271. doi: 10.1038/s41596-024-01044-5. Epub 2024 Sep 5.

DOI:10.1038/s41596-024-01044-5
PMID:39237831
Abstract

One of the foremost challenges in nanobiotechnology is obtaining direct evidence of nanoparticles' absorption and internalization in plants. Although confocal laser scanning microscopy (CLSM) or transmission electron microscopy (TEM) are currently the most commonly used tools to characterize nanoparticles in plants, subjectivity of researchers, incorrect sample handling, inevitable fluorescence leakage and limitations of imaging instruments lead to false positives and non-reproducibility of experimental results. This protocol provides an easy-to-operate dual-step method, combining CLSM for macroscopic tissue examination and TEM for cellular-level analysis, to effectively trace single particles in plant roots with accuracy and precision. In addition, we also provide detailed methods for processing plant materials before imaging, including cleaning, and staining, to maximize the accuracy and reliability of imaging. This protocol involves currently commonly used nanomaterial types, such as metal-based and doped carbon-based materials, and enables accurate localization of nanoparticles with different sizes at the cell level in Arabidopsis thaliana root samples either through contrast or element mapping analysis. It serves as a valuable reference and benchmark for scholars in plant science, chemistry and environmental studies to understand the interaction between plant roots and nanomaterials and to detect the distribution of nanomaterials in plants. Excluding plant culture time, the protocol can be completed in 4-5 d.

摘要

纳米生物技术面临的最主要挑战之一是获取纳米颗粒在植物中吸收和内化的直接证据。尽管共聚焦激光扫描显微镜(CLSM)或透射电子显微镜(TEM)目前是表征植物中纳米颗粒最常用的工具,但研究人员的主观性、不正确的样品处理、不可避免的荧光泄漏以及成像仪器的局限性导致实验结果出现假阳性且不可重复。本方案提供了一种易于操作的两步法,结合CLSM进行宏观组织检查和TEM进行细胞水平分析,以有效且精确地追踪植物根中的单个颗粒。此外,我们还提供了成像前处理植物材料的详细方法,包括清洗和染色,以最大限度地提高成像的准确性和可靠性。本方案涉及当前常用的纳米材料类型,如金属基和掺杂碳基材料,并通过对比或元素映射分析能够在拟南芥根样品的细胞水平上准确地定位不同大小的纳米颗粒。它为植物科学、化学和环境研究领域的学者了解植物根与纳米材料之间的相互作用以及检测纳米材料在植物中的分布提供了有价值的参考和基准。不包括植物培养时间,该方案可在4至5天内完成。

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