Polovinkin Vitaly, Khakurel Krishna, Babiak Michal, Angelov Borislav, Schneider Bohdan, Dohnalek Jan, Andreasson Jakob, Hajdu Janos
ELI Beamlines, Institute of Physics, Czech Academy of Science, Na Slovance 2, 18221 Prague, Czech Republic.
CEITEC - Central European Institute of Technology, Masaryk University, Kamenice 5/4, 62500 Brno, Czech Republic.
J Appl Crystallogr. 2020 Oct 13;53(Pt 6):1416-1424. doi: 10.1107/S1600576720013096. eCollection 2020 Dec 1.
Electron crystallography of sub-micrometre-sized 3D protein crystals has emerged recently as a valuable field of structural biology. crystallization methods, utilizing lipidic mesophases, particularly lipidic cubic phases (LCPs), can produce high-quality 3D crystals of membrane proteins (MPs). A major step towards realizing 3D electron crystallography of MP crystals, grown , is to demonstrate electron diffraction from such crystals. The first task is to remove the viscous and sticky lipidic matrix that surrounds the crystals without damaging the crystals. Additionally, the crystals have to be thin enough to let electrons traverse them without significant multiple scattering. In the present work, the concept that focused ion beam milling at cryogenic temperatures (cryo-FIB milling) can be used to remove excess host lipidic mesophase matrix is experimentally verified, and then the crystals are thinned to a thickness suitable for electron diffraction. In this study, bacteriorhodopsin (BR) crystals grown in a lipidic cubic mesophase of monoolein were used as a model system. LCP from a part of a hexagon-shaped plate-like BR crystal (∼10 µm in thickness and ∼70 µm in the longest dimension), which was flash-frozen in liquid nitro-gen, was milled away with a gallium FIB under cryogenic conditions, and a part of the crystal itself was thinned into a ∼210 nm-thick lamella with the ion beam. The frozen sample was then transferred into an electron cryo-microscope, and a nanovolume of ∼1400 × 1400 × 210 nm of the BR lamella was exposed to 200 kV electrons at a fluence of ∼0.06 e Å. The resulting electron diffraction peaks were detected beyond 2.7 Å resolution (with an average peak height to background ratio of >2) by a CMOS-based Ceta 16M camera. The results demonstrate that cryo-FIB milling produces high-quality lamellae from crystals grown in lipidic mesophases and pave the way for 3D electron crystallography on crystals grown or embedded in highly viscous media.
亚微米级三维蛋白质晶体的电子晶体学最近已成为结构生物学的一个重要领域。利用脂质中间相,特别是脂质立方相(LCP)的结晶方法,可以产生高质量的膜蛋白(MP)三维晶体。实现生长的MP晶体三维电子晶体学的一个主要步骤是证明来自此类晶体的电子衍射。首要任务是去除围绕晶体的粘性脂质基质,同时不损坏晶体。此外,晶体必须足够薄,以便电子能够穿过而不会发生显著的多重散射。在本工作中,通过实验验证了低温聚焦离子束铣削(cryo-FIB铣削)可用于去除多余的主体脂质中间相基质这一概念,然后将晶体减薄至适合电子衍射的厚度。在本研究中,以在单油酸脂质立方中间相中生长的细菌视紫红质(BR)晶体作为模型系统。将一块六边形板状BR晶体(厚度约10μm,最长尺寸约70μm)的一部分在液氮中快速冷冻,在低温条件下用镓聚焦离子束铣去其脂质立方相,并用离子束将晶体的一部分减薄成约210nm厚的薄片。然后将冷冻样品转移到电子冷冻显微镜中,将约1400×1400×210nm的BR薄片纳米体积暴露于200kV电子下,注量约为0.06e/Å。基于CMOS的Ceta 16M相机在2.7Å分辨率以上检测到了所得的电子衍射峰(平均峰高与背景比>2)。结果表明,低温聚焦离子束铣削可从脂质中间相中生长的晶体产生高质量薄片,为在高粘性介质中生长或嵌入的晶体进行三维电子晶体学研究铺平了道路。