Höppener Christiane, Novotny Lukas
The Institute of Optics and Department of Biomedical Engineering, University of Rochester, Rochester, New York 14627, USA.
Nano Lett. 2008 Feb;8(2):642-6. doi: 10.1021/nl073057t. Epub 2008 Jan 30.
Understanding the diversity of biological processes requires methods that can address single proteins in their natural environment and provide insights into structural and functional properties, as well as the local distribution of each individual protein. We use an optical antenna in the form of a single gold nanoparticle to localize incident laser radiation to 50 nm, significantly smaller than the diffraction limit of light. Our approach enables us to optically resolve individual plasma-membrane-bound Ca2+ pumps (PMCA4) immersed in aqueous environments and to determine the distribution of interprotein distances. We are able to correlate the protein maps with local topology. Improved antenna geometries will make it possible to resolve, identify, and probe single membrane proteins in live cells with true protein resolution of 5-10 nm.
了解生物过程的多样性需要能够在天然环境中研究单个蛋白质,并深入了解其结构和功能特性以及每个蛋白质的局部分布的方法。我们使用单个金纳米颗粒形式的光学天线将入射激光辐射聚焦到50纳米,这比光的衍射极限小得多。我们的方法使我们能够通过光学手段分辨浸没在水性环境中的单个质膜结合Ca2+泵(PMCA4),并确定蛋白质间距离的分布。我们能够将蛋白质图谱与局部拓扑结构相关联。改进的天线几何结构将使以5-10纳米的真实蛋白质分辨率分辨、识别和探测活细胞中的单个膜蛋白成为可能。