Suppr超能文献

单分子扩散成像

Imaging of single molecule diffusion.

作者信息

Schmidt T, Schütz G J, Baumgartner W, Gruber H J, Schindler H

机构信息

Institute for Biophysics, University of Linz, Austria.

出版信息

Proc Natl Acad Sci U S A. 1996 Apr 2;93(7):2926-9. doi: 10.1073/pnas.93.7.2926.

Abstract

In recent years observations at the level of individual atoms and molecules became possible by microscopy and spectroscopy. Imaging of single fluorescence molecules has been achieved but has so far been restricted to molecules in the immobile state. Here we provide methodology for visualization of the motion of individual fluorescent molecules. It is applied to imaging of the diffusional path of single molecules in a phospholipid membrane by using phospholipids carrying one rhodamine dye molecule. For this methodology, fluorescence microscopy was carried to a sensitivity so that single fluorescent molecules illuminated for only 5 ms were resolvable at a signal/noise ratio of 28. Repeated illuminations permitted direct observation of the diffusional motion of individual molecules with a positional accuracy of 30 nm. Such capability has fascinating potentials in bioscience--for example, to correlate biological functions of cell membranes with movements, spatial organization, and stoichiometries of individual components.

摘要

近年来,借助显微镜和光谱学技术,在单个原子和分子层面进行观测已成为可能。单个荧光分子的成像已得以实现,但迄今为止仅限于处于静止状态的分子。在此,我们提供了一种用于可视化单个荧光分子运动的方法。该方法通过使用携带一个罗丹明染料分子的磷脂,应用于磷脂膜中单个分子扩散路径的成像。对于此方法,荧光显微镜的灵敏度达到了仅被照射5毫秒的单个荧光分子在信噪比为28时仍可分辨的程度。重复照射使得能够以30纳米的位置精度直接观测单个分子的扩散运动。这种能力在生物科学领域具有迷人的潜力——例如,将细胞膜的生物学功能与单个组分的运动、空间组织和化学计量学联系起来。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验