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In vivo X-ray elemental imaging of single cell model organisms manipulated by laser-based optical tweezers

机译:基于激光的镊子对单细胞模型生物的体内 X射线元素成像

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We report on a radically new elemental imaging approach for the analysis of biological model organisms and single cells in their natural, in vivo state. The methodology combines optical tweezers (OT) technology for non-contact, laser-based sample manipulation with synchrotron radiation confocal X-ray fluorescence (XRF) microimaging for the first time. The main objective of this work is to establish a new method for in vivo elemental imaging in a two-dimensional (2D) projection mode in free-standing biological microorganisms or single cells, present in their aqueous environment. Using the model organism Scrippsiella trochoidea , a first proof of principle experiment at beamline ID13 of the European Synchrotron Radiation Facility (ESRF) demonstrates the feasibility of the OT XRF methodology, which is applied to study mixture toxicity of Cu-Ni and Cu-Zn as a result of elevated exposure. We expect that the new OT XRF methodology will significantly contribute to the new trend of investigating microorganisms at the cellular level with added in vivo capability.
机译:我们报告了一种根本新的元素成像方法,用于分析生物模型生物和处于自然,体内状态的单细胞。该方法首次将用于非接触式,基于激光的样品处理的光镊(OT)技术与同步加速器共聚焦X射线荧光(XRF)微成像技术相结合。这项工作的主要目的是为存在于其水性环境中的独立式生物微生物或单细胞建立二维(2D)投影模式的体内元素成像新方法。欧洲模式同步辐射设施(ESRF)在射线束ID13上使用模式生物Sctropsiella trochoidea进行的原理验证的第一个实验证明了OT XRF方法的可行性,该方法可用于研究Cu-Ni和Cu-Zn暴露量增加的结果。我们期望新的OT XRF方法将大大有助于研究在细胞水平上增加了体内功能的微生物的新趋势。

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