Laboratoire de Recherche en Nanosciences EA 4682, UFR Sciences Exactes et Naturelles, Université de Reims Champagne Ardenne, 21 rue Clément ADER, Reims, France.
J Struct Biol. 2012 Nov;180(2):352-61. doi: 10.1016/j.jsb.2012.08.011. Epub 2012 Sep 7.
Cryo fluorescence imaging coupled with the cryo-EM technique (cryo-CLEM) avoids chemical fixation and embedding in plastic, and is the gold standard for correlated imaging in a close to native state. This multi-modal approach has not previously included elementary nano analysis or evaluation of water content. We developed a new approach allowing analysis of targeted in situ intracellular ions and water measurements at the nanoscale (EDXS and STEM dark field imaging) within domains identified by examination of specific GFP-tagged proteins. This method allows both water and ions- fundamental to cell biology- to be located and quantified at the subcellular level. We illustrate the potential of this approach by investigating changes in water and ion content in nuclear domains identified by GFP-tagged proteins in cells stressed by Actinomycin D treatment and controls. The resolution of our approach was sufficient to distinguish clumps of condensed chromatin from surrounding nucleoplasm by fluorescence imaging and to perform nano analysis in this targeted compartment.
冷冻荧光成像与冷冻电镜技术(cryo-CLEM)相结合,避免了化学固定和塑料包埋,是接近自然状态下相关成像的金标准。这种多模态方法以前没有包括基本的纳米分析或水含量的评估。我们开发了一种新方法,允许在通过检查特定 GFP 标记蛋白确定的域内进行靶向原位细胞内离子和水测量的纳米分析(EDXS 和 STEM 暗场成像)。该方法允许在亚细胞水平上定位和定量水和离子 - 这对细胞生物学至关重要。我们通过研究 Actinomycin D 处理和对照细胞中 GFP 标记蛋白鉴定的核域中的水和离子含量的变化来证明这种方法的潜力。我们的方法的分辨率足以通过荧光成像将浓缩染色质的团块与周围核质区分开来,并在这个靶向隔室中进行纳米分析。