Microcrystal preparation for serial femtosecond X‐ray crystallography of bacterial copper amine oxidase. Issue 10 (4th October 2021)

• Record Type: Journal Article
• Authors: Murakawa, Takeshi; Suzuki, Mamoru; Arima, Toshi; Sugahara, Michihiro; Tanaka, Tomoyuki; Tanaka, Rie; Iwata, So; Nango, Eriko; Tono, Kensuke; Hayashi, Hideyuki; Fukui, Kenji; Yano, Takato; Tanizawa, Katsuyuki; Okajima, Toshihide
• Is Part Of: Acta crystallographica. Volume 77:Issue 10(2021)
• Page Start: 356
• Page End: 363
• Publication Date: 2021-10-04
• Subjects: serial femtosecond X‐ray crystallography -- X‐ray free‐electron lasers -- radiation‐damage‐free protein structure -- copper amine oxidase -- microcrystals; Crystallography -- Periodicals; Crystals -- Periodicals; 548
• DOI: 10.1107/S2053230X21008967
• Languages: English
• ISSNs: 2053-230X

Abstract

Abstract : Microcrystals of bacterial copper amine oxidase were prepared by combining micro‐seeding and batch crystallization, and were used to determine a radiation‐damage‐free, nonfrozen structure by serial femtosecond X‐ray crystallography. Abstract : Recent advances in serial femtosecond X‐ray crystallography (SFX) using X‐ray free‐electron lasers have paved the way for determining radiation‐damage‐free protein structures under nonfreezing conditions. However, the large‐scale preparation of high‐quality microcrystals of uniform size is a prerequisite for SFX, and this has been a barrier to its widespread application. Here, a convenient method for preparing high‐quality microcrystals of a bacterial quinoprotein enzyme, copper amine oxidase from Arthrobacter globiformis, is reported. The method consists of the mechanical crushing of large crystals (5–15 mm 3 ), seeding the crushed crystals into the enzyme solution and standing for 1 h at an ambient temperature of ∼26°C, leading to the rapid formation of microcrystals with a uniform size of 3–5 µm. The microcrystals diffracted X‐rays to a resolution beyond 2.0 Å in SFX measurements at the SPring‐8 Angstrom Compact Free Electron Laser facility. The damage‐free structure determined at 2.2 Å resolution was essentially identical to that determined previously by cryogenic crystallography using synchrotron X‐ray radiation.