Cryo-EM samples of gas-phase purified protein assemblies using native electrospray ion-beam deposition

被引:15
作者
Esser, Tim K. [1 ]
Bohning, Jan [2 ]
Fremdling, Paul [1 ]
Bharat, Tanmay [2 ,3 ]
Gault, Joseph [1 ,5 ]
Rauschenbach, Stephan [1 ,4 ]
机构
[1] Univ Oxford, Dept Chem, Oxford OX1 3TF, England
[2] Univ Oxford, Sir William Dunn Sch Pathol, South Parks Rd, Oxford OX1 3RE, England
[3] MRC Lab Mol Biol, Struct Studies Div, Francis Crick Ave, Cambridge CB2 0QH, England
[4] Max Planck Inst Solid State Res, Heisenbergstr 1, DE-70569 Stuttgart, Germany
[5] Vertex Pharmaceut, 86-88 Jubilee Ave,Milton Pk, Abingdon OX14 4RW, Oxon, England
基金
英国生物技术与生命科学研究理事会; 英国工程与自然科学研究理事会; 英国惠康基金;
关键词
MASS-SPECTROMETRY; CYTOCHROME-C; SOFT; MICROSCOPY; RESOLUTION; GRAPHENE; FROZEN;
D O I
10.1039/d2fd00065b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
An increasing number of studies on biomolecular function indirectly combine mass spectrometry (MS) with imaging techniques such as cryo electron microscopy (cryo-EM). This approach allows information on the homogeneity, stoichiometry, shape, and interactions of native protein complexes to be obtained, complementary to high-resolution protein structures. We have recently demonstrated TEM sample preparation via native electrospray ion-beam deposition (ES-IBD) as a direct link between native MS and cryo-EM. This workflow forms a potential new route to the reliable preparation of homogeneous cryo-EM samples and a better understanding of the relation between native solution-phase and native-like gas-phase structures. However, many aspects of the workflow need to be understood and optimized to obtain performance comparable to that of state-of-the-art cryo-EM. Here, we expand on the previous discussion of key factors by probing the effects of substrate type and deposition energy. We present and discuss micrographs from native ES-IBD samples with amorphous carbon, graphene, and graphene oxide, as well as landing energies in the range between 2 and 150 eV per charge.
引用
收藏
页码:67 / 80
页数:14
相关论文
共 51 条
[1]   Two-dimensional honeycomb network through sequence-controlled self-assembly of oligopeptides [J].
Abb, Sabine ;
Harnau, Ludger ;
Gutzler, Rico ;
Rauschenbach, Stephan ;
Kern, Klaus .
NATURE COMMUNICATIONS, 2016, 7
[2]   Exploring the Molecular Conformation Space by Soft Molecule- Surface Collision [J].
Anggara, Kelvin ;
Zhu, Yuntao ;
Delbianco, Martina ;
Rauschenbach, Stephan ;
Abb, Sabine ;
Seeberger, Peter H. ;
Kern, Klaus .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2020, 142 (51) :21420-21427
[3]   Controlled deposition of size-selected silver nanoclusters [J].
Bromann, K ;
Felix, C ;
Brune, H ;
Harbich, W ;
Monot, R ;
Buttet, J ;
Kern, K .
SCIENCE, 1996, 274 (5289) :956-958
[4]   Cryo-electron microscopy structure and analysis of the P-Rex1-Gβγ signaling scaffold [J].
Cash, Jennifer N. ;
Urata, Sarah ;
Li, Sheng ;
Ravala, Sandeep K. ;
Avramova, Larisa, V ;
Shost, Michael D. ;
Gutkind, J. Silvio ;
Tesmer, John J. G. ;
Cianfrocco, Michael A. .
SCIENCE ADVANCES, 2019, 5 (10)
[5]   Low-Energy Ionic Collisions at Molecular Solids [J].
Cyriac, Jobin ;
Pradeep, T. ;
Kang, H. ;
Souda, R. ;
Cooks, R. G. .
CHEMICAL REVIEWS, 2012, 112 (10) :5356-5411
[6]   Architecture of the yeast Elongator complex [J].
Dauden, Maria I. ;
Kosinski, Jan ;
Kolaj-Robin, Olga ;
Desfosses, Ambroise ;
Ori, Alessandro ;
Faux, Celine ;
Hoffmann, Niklas A. ;
Onuma, Osita F. ;
Breunig, Karin D. ;
Beck, Martin ;
Sachse, Carsten ;
Seraphin, Bertrand ;
Glatt, Sebastian ;
Mueller, Christoph W. .
EMBO REPORTS, 2017, 18 (02) :264-279
[7]   A Close Look at Proteins: Submolecular Resolution of Two- and Three-Dimensionally Folded Cytochrome c at Surfaces [J].
Deng, Zhitao ;
Thontasen, Nicha ;
Malinowski, Nikola ;
Rinke, Gordon ;
Harnau, Ludger ;
Rauschenbach, Stephan ;
Kern, Klaus .
NANO LETTERS, 2012, 12 (05) :2452-2458
[8]   ELECTRON-MICROSCOPY OF FROZEN WATER AND AQUEOUS-SOLUTIONS [J].
DUBOCHET, J ;
LEPAULT, J ;
FREEMAN, R ;
BERRIMAN, JA ;
HOMO, JC .
JOURNAL OF MICROSCOPY, 1982, 128 (DEC) :219-237
[9]  
Esser T.K., 2021, BIORXIV, DOI [10.1101/2021.10.18.464782, DOI 10.1101/2021.10.18.464782]
[10]  
Frank J., 2006, Three-Dimensional Electron Microscopy of Macromolecular Assemblies: Visualization of Biological Molecules in Their Native State