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用于室温下水合生物样品分子成像的简便密封透射电子显微镜网格制备方法。

Facile hermetic TEM grid preparation for molecular imaging of hydrated biological samples at room temperature.

作者信息

Kong Lingli, Liu Jianfang, Zhang Meng, Lu Zhuoyang, Xue Han, Ren Amy, Liu Jiankang, Li Jinping, Li Ling Wai, Ren Gang

机构信息

The Molecular Foundry, Lawrence Berkeley National Laboratory, Berkeley, CA 94720.

School of Life Science and Technology, and Frontier Institute of Science and Technology, Xi'an Jiaotong University, Xi'an, China.

出版信息

Res Sq. 2023 Feb 14:rs.3.rs-2464569. doi: 10.21203/rs.3.rs-2464569/v1.

Abstract

Although structures of vitrified supramolecular complexes have been determined at near-atomic resolution, elucidating molecular structure in living cells remains a major challenge. Here, we apply a novel but simple liquid-cell technique, developed previously for real-time imaging of the dynamics at a liquid-gas interface, to image wet biological samples. With extra scattering from the liquid phase, the transmission electron micrographs show amplitude contrast comparable to that in negatively stained samples. Single-molecule domains are resolved in the protein complex GroEL imaged in buffer solution at room temperature. Moreover, various stages of virus cell entry, which are transient events with very few structural information to date, are also captured. Morphological details are reconstructed using the technique of individual particle electron tomography. These results demonstrate that this approach can be a valuable yet cost-effective technique complementary to other microscopy techniques for addressing important biological questions at the molecular level.

摘要

尽管玻璃化超分子复合物的结构已在近原子分辨率下得以确定,但阐明活细胞中的分子结构仍是一项重大挑战。在此,我们应用一种新颖但简单的液池技术(该技术先前已开发用于在液-气界面实时成像动力学)对湿生物样品进行成像。由于液相产生的额外散射,透射电子显微照片显示出与负染色样品相当的振幅对比度。在室温下于缓冲溶液中成像的蛋白质复合物GroEL中分辨出了单分子结构域。此外,还捕获到了病毒细胞进入的各个阶段,这些阶段是迄今结构信息极少的瞬态事件。利用单颗粒电子断层扫描技术重建了形态细节。这些结果表明,这种方法可能是一种有价值且经济高效的技术,可作为其他显微镜技术的补充,用于在分子水平解决重要的生物学问题。

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