High-resolution cryo-EM using a common LaB6 120-keV electron microscope equipped with a sub-200-keV direct electron detector

被引:0
|
作者
Venugopal, Hariprasad [1 ]
Mobbs, Jesse [2 ,3 ]
Taveneau, Cyntia [4 ]
Fox, Daniel R. [3 ,5 ,6 ]
Vuckovic, Ziva [4 ]
Gulati, Sahil [7 ]
Knott, Gavin [8 ]
Grinter, Rhys [3 ,5 ,6 ]
Thal, David [2 ,3 ]
Mick, Stephen [7 ]
Czarnik, Cory [7 ]
Ramm, Georg [1 ,8 ]
机构
[1] Monash Univ, Ramaciotti Ctr Cryoelectron Microscopy, Clayton, Vic, Australia
[2] Monash Univ, Monash Inst Pharmaceut Sci, Drug Discovery Biol, Parkville, Vic, Australia
[3] Monash Univ, Monash Inst Pharmaceut Sci, Australian Res Council, Ctr Cryoelectron Microscopy Membrane Prot, Parkville, Vic, Australia
[4] Glycoera AG, Einsiedlerstr 34, CH-8820 Wadenswil, Switzerland
[5] Monash Univ, Biomed Discovery Inst, Dept Microbiol, Clayton, Vic 3800, Australia
[6] Univ Melbourne, Bio21 Mol Sci & Biotechnol Inst, Dept Biochem & Pharmacol, Parkville, Vic, Australia
[7] Gatan Inc, Pleasanton, CA USA
[8] Monash Univ, Monash Biomed Discovery Inst, Dept Biochem & Mol Biol, Melbourne, Vic, Australia
来源
SCIENCE ADVANCES | 2025年 / 11卷 / 01期
基金
澳大利亚国家健康与医学研究理事会; 澳大利亚研究理事会;
关键词
BEAM-INDUCED MOTION; STRUCTURAL BASIS; IMAGES; CRYOMICROSCOPY;
D O I
10.1126/sciadv.adr0438
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
High-resolution cryo-electron microscopy (cryo-EM) requires costly 200- to 300-keV cryo-transmission electron microscopes (cryo-TEMs) with field emission gun (FEG) sources, stable columns, constant-powered lenses, autoloader, and direct electron detectors (DED). Recent advances in 100-keV imaging with the emergence of sub-200-keV optimized DED technology promises the development of more affordable cryo-TEMs. So far, 100-keV imaging has required microscopes with FEG sources. We here explored whether a standard 120-keV TEMs with thermionic lanthanum hexaboride (LaB6) source can be upgraded with a sub-200-keV DED for high-resolution cryo-EM. Using this imaging configuration, we successfully obtained a 2.65 & Aring; reconstruction for apoferritin, 4.33 & Aring; for 64-kDa hemoglobin, and 4.4 & Aring; for an asymmetric 153kDa membrane protein GPCR. All results were achieved using standard automated data collection with SerialEM, demonstrating the feasibility to collect large cryo-EM datasets with a side-entry cryo-holder. These results showcase a widely accessible solution to obtaining interpretable cryo-EM structures at low cost and contribute to the "democratization" of cryo-EM.
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页数:11
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