Physics Department, Stanford University, 382 Via Pueblo Mall, Stanford, California, 94305, USA.
National Center for Electron Microscopy, Molecular Foundry, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, California, 94720, USA.
Sci Rep. 2017 May 10;7(1):1699. doi: 10.1038/s41598-017-01841-x.
Feynman once asked physicists to build better electron microscopes to be able to watch biology at work. While electron microscopes can now provide atomic resolution, electron beam induced specimen damage precludes high resolution imaging of sensitive materials, such as single proteins or polymers. Here, we use simulations to show that an electron microscope based on a multi-pass measurement protocol enables imaging of single proteins, without averaging structures over multiple images. While we demonstrate the method for particular imaging targets, the approach is broadly applicable and is expected to improve resolution and sensitivity for a range of electron microscopy imaging modalities, including, for example, scanning and spectroscopic techniques. The approach implements a quantum mechanically optimal strategy which under idealized conditions can be considered interaction-free.
费曼曾要求物理学家制造更好的电子显微镜,以便能够观察生物的工作过程。虽然电子显微镜现在可以提供原子分辨率,但电子束诱导的样品损伤排除了对敏感材料(如单个蛋白质或聚合物)的高分辨率成像。在这里,我们使用模拟表明,基于多通测量协议的电子显微镜能够对单个蛋白质进行成像,而无需对多个图像中的结构进行平均。虽然我们针对特定的成像目标演示了该方法,但该方法具有广泛的适用性,有望提高一系列电子显微镜成像模式的分辨率和灵敏度,例如,扫描和光谱技术。该方法实现了一种量子力学上最优的策略,在理想条件下可以被认为是无相互作用的。