Vergucht Eva, Brans Toon, Beunis Filip, Garrevoet Jan, De Rijcke Maarten, Bauters Stephen, Deruytter David, Vandegehuchte Michiel, Van Nieuwenhove Ine, Janssen Colin, Burghammer Manfred, Vincze Laszlo
X-ray Microspectroscopy and Imaging Group, Ghent University, Krijgslaan 281 (S12), B-9000 Ghent, Belgium.
1] Department of Electronics and Information Systems, Ghent University, Sint-Pietersnieuwstraat 41, B-9000 Ghent, Belgium [2] Center for Nano and Biophotonics, Ghent University, Sint-Pietersnieuwstraat 41, B-9000 Ghent, Belgium.
Sci Rep. 2015 Mar 12;5:9049. doi: 10.1038/srep09049.
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.
我们报道了一种全新的元素成像方法,用于分析处于自然活体状态的生物模型生物体和单细胞。该方法首次将用于非接触式、基于激光的样品操控的光镊(OT)技术与同步辐射共聚焦X射线荧光(XRF)显微成像相结合。这项工作的主要目标是建立一种新方法,用于在二维(2D)投影模式下对处于水环境中的独立生物微生物或单细胞进行体内元素成像。使用海洋原甲藻(Scrippsiella trochoidea)作为模式生物体,在欧洲同步辐射装置(ESRF)的ID13光束线进行的首次原理验证实验证明了光镊XRF方法的可行性,该方法被用于研究因暴露增加导致的铜镍和铜锌混合毒性。我们预计,新的光镊XRF方法将显著推动在细胞水平研究微生物并增加体内研究能力这一新趋势的发展。