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4DC7

Crystal Structure of Myoglobin Exposed to Excessive SONICC Imaging Laser Dose.

Summary for 4DC7
Entry DOI10.2210/pdb4dc7/pdb
Related4DC8
DescriptorMyoglobin, PROTOPORPHYRIN IX CONTAINING FE, SULFATE ION, ... (4 entities in total)
Functional Keywordssonicc, oxygen storage
Biological sourceEquus caballus (domestic horse,equine)
Total number of polymer chains1
Total formula weight17831.14
Authors
Becker, M.,Mulichak, A.M.,Kissick, D.J.,Fischetti, R.F.,Keefe, L.J.,Simpson, G.J. (deposition date: 2012-01-17, release date: 2013-01-23, Last modification date: 2024-02-28)
Primary citationKissick, D.J.,Dettmar, C.M.,Becker, M.,Mulichak, A.M.,Cherezov, V.,Ginell, S.L.,Battaile, K.P.,Keefe, L.J.,Fischetti, R.F.,Simpson, G.J.
Towards protein-crystal centering using second-harmonic generation (SHG) microscopy.
Acta Crystallogr.,Sect.D, 69:843-851, 2013
Cited by
PubMed Abstract: The potential of second-harmonic generation (SHG) microscopy for automated crystal centering to guide synchrotron X-ray diffraction of protein crystals was explored. These studies included (i) comparison of microcrystal positions in cryoloops as determined by SHG imaging and by X-ray diffraction rastering and (ii) X-ray structure determinations of selected proteins to investigate the potential for laser-induced damage from SHG imaging. In studies using β2 adrenergic receptor membrane-protein crystals prepared in lipidic mesophase, the crystal locations identified by SHG images obtained in transmission mode were found to correlate well with the crystal locations identified by raster scanning using an X-ray minibeam. SHG imaging was found to provide about 2 µm spatial resolution and shorter image-acquisition times. The general insensitivity of SHG images to optical scatter enabled the reliable identification of microcrystals within opaque cryocooled lipidic mesophases that were not identified by conventional bright-field imaging. The potential impact of extended exposure of protein crystals to five times a typical imaging dose from an ultrafast laser source was also assessed. Measurements of myoglobin and thaumatin crystals resulted in no statistically significant differences between structures obtained from diffraction data acquired from exposed and unexposed regions of single crystals. Practical constraints for integrating SHG imaging into an active beamline for routine automated crystal centering are discussed.
PubMed: 23633594
DOI: 10.1107/S0907444913002746
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.5 Å)
Structure validation

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数据于2025-06-25公开中

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