Misevic Gradimir N, Rasser Bernard, Norris Vic, Dérue Cédric, Gibouin David, Lefebvre Fabrice, Verdus Marie-Claire, Delaune Anthony, Legent Guillaume, Ripoll Camille
Faculté des Sciences de l'Université de Rouen, 76 821, Mont Saint Aignan Cedex, France.
Methods Mol Biol. 2009;522:163-73. doi: 10.1007/978-1-59745-413-1_10.
3D chemical microscopy is one of the emerging applications of secondary ion mass spectrometry (SIMS) in biology. Tissues, cells, extracellular matrices, and polymer films can be imaged at present with a lateral resolution of 50 nm and depth resolution of 1 nm using the latest generation of CAMECA magnetic sector NanoSIMS 50 or with a lower lateral resolution (above 100 nm) using IMS 4f Cameca SIMS equipped with cold stage. Dynamic mode SIMS analysis is performed in ultrahigh vacuum and thus requires specific and careful preparation of biological samples aimed at preserving and minimizing destruction of the original structural and chemical properties of the samples. Here we describe a methodology based on the ultrafast plunge-freezing of biological tissues, preparation of the sample for SIMS analyses and transfer to the SIMS cold stage without interruption of the cold chain during the mounting procedure and subsequent SIMS analyses. Using this strategy, SIMS chemical microscopy can be performed on biological tissue in which unwanted molecular and/or structural reorganization, loss of constituents and chemical modifications are minimized and in which structures are therefore optimally preserved.
三维化学显微镜是二次离子质谱(SIMS)在生物学领域新兴的应用之一。目前,使用最新一代的CAMECA磁扇形NanoSIMS 50,可对组织、细胞、细胞外基质和聚合物薄膜进行成像,横向分辨率为50纳米,深度分辨率为1纳米;或者使用配备冷台的IMS 4f Cameca SIMS,横向分辨率较低(高于100纳米)。动态模式SIMS分析在超高真空下进行,因此需要对生物样品进行特殊且细致的制备,目的是保存并尽量减少对样品原始结构和化学性质的破坏。在此,我们描述一种基于生物组织超快骤冷的方法,用于制备SIMS分析样品,并在安装过程及后续SIMS分析期间,在不中断冷链的情况下将样品转移至SIMS冷台。采用这种策略,可对生物组织进行SIMS化学显微镜分析,其中不必要的分子和/或结构重组、成分损失和化学修饰被降至最低,从而使结构得到最佳保存。