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7ASX

Fixed-target serial femtosecond crystallography using in cellulo grown Neurospora crassa HEX-1 microcrystals. (Chip 1)

7ASX の概要
エントリーDOI10.2210/pdb7asx/pdb
関連するPDBエントリー7ASI
分子名称eIF-5a domain-containing protein (2 entities in total)
機能のキーワードin cellulo crystals, woronin body, septal pore sealing, structural protein
由来する生物種Neurospora crassa
タンパク質・核酸の鎖数1
化学式量合計19221.74
構造登録者
Lahey-Rudolph, J.M.,Schoenherr, R.,Barthelmess, M.,Fischer, P.,Seuring, C.,Wagner, A.,Meents, A.,Redecke, L. (登録日: 2020-10-28, 公開日: 2021-06-23, 最終更新日: 2024-01-31)
主引用文献Lahey-Rudolph, J.M.,Schonherr, R.,Barthelmess, M.,Fischer, P.,Seuring, C.,Wagner, A.,Meents, A.,Redecke, L.
Fixed-target serial femtosecond crystallography using in cellulo grown microcrystals.
Iucrj, 8:665-677, 2021
Cited by
PubMed Abstract: The crystallization of recombinant proteins in living cells is an exciting new approach in structural biology. Recent success has highlighted the need for fast and efficient diffraction data collection, optimally directly exposing intact crystal-containing cells to the X-ray beam, thus protecting the crystals from environmental challenges. Serial femtosecond crystallography (SFX) at free-electron lasers (XFELs) allows the collection of detectable diffraction even from tiny protein crystals, but requires very fast sample exchange to utilize each XFEL pulse. Here, an efficient approach is presented for high-resolution structure elucidation using serial femtosecond diffraction of micometre-sized crystals of the protein HEX-1 from the fungus on a fixed target. Employing the fast and highly accurate Roadrunner II translation-stage system allowed efficient raster scanning of the pores of micro-patterned, single-crystalline silicon chips loaded with living, crystal-containing insect cells. Compared with liquid-jet and LCP injection systems, the increased hit rates of up to 30% and reduced background scattering enabled elucidation of the HEX-1 structure. Using diffraction data from only a single chip collected within 12 min at the Linac Coherent Light Source, a 1.8 Å resolution structure was obtained with significantly reduced sample consumption compared with previous SFX experiments using liquid-jet injection. This HEX-1 structure is almost superimposable with that previously determined using synchrotron radiation from single HEX-1 crystals grown by sitting-drop vapour diffusion, validating the approach. This study demonstrates that fixed-target SFX using micro-patterned silicon chips is ideally suited for efficient diffraction data collection using living, crystal-containing cells, and offers huge potential for the straightforward structure elucidation of proteins that form intracellular crystals at both XFELs and synchrotron sources.
PubMed: 34258014
DOI: 10.1107/S2052252521005297
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.8 Å)
構造検証レポート
Validation report summary of 7asx
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-11-13に公開中

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