Latychevskaia Tatiana, Longchamp Jean-Nicolas, Escher Conrad, Fink Hans-Werner
Physics Department, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland.
Physics Department, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland.
Ultramicroscopy. 2015 Dec;159 Pt 2:395-402. doi: 10.1016/j.ultramic.2014.11.024. Epub 2014 Dec 2.
The current state of the art in structural biology is led by NMR, X-ray crystallography and TEM investigations. These powerful tools however all rely on averaging over a large ensemble of molecules. Here, we present an alternative concept aiming at structural analysis at the single molecule level. We show that by combining electron holography and coherent diffraction imaging estimations concerning the phase of the scattered wave become needless as the phase information is extracted from the data directly and unambiguously. Performed with low-energy electrons the resolution of this lens-less microscope is just limited by the De Broglie wavelength of the electron wave and the numerical aperture, given by detector geometry. In imaging freestanding graphene, a resolution of 2Å has been achieved revealing the 660.000 unit cells of the graphene sheet from a single data set. Once applied to individual biomolecules the method shall ultimately allow for non-destructive imaging and imports the potential to distinguish between different conformations of proteins with atomic resolution.
结构生物学的当前技术水平由核磁共振(NMR)、X射线晶体学和透射电子显微镜(TEM)研究主导。然而,这些强大的工具都依赖于对大量分子集合进行平均。在此,我们提出一种旨在进行单分子水平结构分析的替代概念。我们表明,通过将电子全息术和相干衍射成像相结合,由于相位信息是直接且明确地从数据中提取的,因此无需对散射波的相位进行估计。使用低能电子进行操作时,这种无透镜显微镜的分辨率仅受电子波的德布罗意波长和由探测器几何形状给出的数值孔径的限制。在对独立的石墨烯进行成像时,已实现了2埃的分辨率,从单个数据集揭示了石墨烯片的660,000个晶胞。一旦应用于单个生物分子,该方法最终将允许进行无损成像,并具有以原子分辨率区分蛋白质不同构象的潜力。