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采用飞行时间二次离子质谱法在单细胞水平上进行原子和分子成像。

Atomic and molecular imaging at the single-cell level with TOF-SIMS.

作者信息

Colliver T L, Brummel C L, Pacholski M L, Swanek F D, Ewing A G, Winograd N

机构信息

Department of Chemistry, Pennsylvania State University, University Park 16802, USA.

出版信息

Anal Chem. 1997 Jul 1;69(13):2225-31. doi: 10.1021/ac9701748.

Abstract

A complete cold chain freeze-fracture methodology has been developed to test the feasibility of using time-of-flight secondary ion mass spectrometry (TOF-SIMS) imaging for the molecular analysis of frozen hydrated biological samples. Because the technique only samples the first few monolayers of a sample, water on the surface of a sample can be a major source of interference. This problem can be minimized by placing a cold trap (fracture knife and housing at -196 degrees C) near the fractured sample that is held at a warmer temperature (-97 to -113 degrees C). This results in removal of surface water and prevents condensation on the surface. Although this approach is effective, it has been found that sample warming needs to be carefully controlled due to the volatility of other matrix molecules and the morphological effects imparted onto the cell surface during drying. By utilizing the above handling technique, it has been possible to demonstrate for the first time that TOF-SIMS imaging technology can be used to obtain images of molecular species across a cell surface with a submicrometer ion probe beam. Images of small hydrocarbons and the deliberately added dopants DMSO and cocaine have been obtained with TOF-SIMS of the single-cell organism Paramecium.

摘要

已开发出一种完整的冷链冷冻断裂方法,以测试使用飞行时间二次离子质谱(TOF-SIMS)成像对冷冻水合生物样品进行分子分析的可行性。由于该技术仅对样品的前几个单分子层进行采样,样品表面的水可能是主要干扰源。通过将冷阱(断裂刀和外壳温度为-196℃)放置在保持在较高温度(-97至-113℃)的断裂样品附近,可将此问题最小化。这会导致表面水的去除并防止表面冷凝。尽管这种方法有效,但已发现由于其他基质分子的挥发性以及干燥过程中赋予细胞表面的形态学效应,样品升温需要仔细控制。通过利用上述处理技术,首次证明了TOF-SIMS成像技术可用于使用亚微米离子探测束在细胞表面获得分子种类的图像。已通过单细胞生物草履虫的TOF-SIMS获得了小分子烃以及特意添加的掺杂剂二甲基亚砜(DMSO)和可卡因的图像。

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