Serial millisecond crystallography of membrane and soluble protein microcrystals using synchrotron radiation

Martin-Garcia, J.M.; Conrad, C.E.; Nelson, G.; Stander, N.; Zatsepin, N.A.; Zook, J.; Zhu, L.; Geiger, J.; Chun, E.; Kissick, D.; Hilgart, M.C.; Ogata, C.; Ishchenko, A.; Nagaratnam, N.; Roy-Chowdhury, S.; Coe, J.; Subramanian, G.; Schaffer, A.; James, D.; Ketwala, G.; Venugopalan, N.; Xu, S.; Corcoran, S.; Ferguson, D.; Weierstall, U.; Spence, J.C.H.; Cherezov, V.; Fromme, P.; Fischetti, R.F.; Liu, W.

doi:10.1107/S205225251700570X

Figure 8
Diffuse background scattering comparison between PEO gel and LCP. The mean radial intensity over the total number of frames used for each medium protein is plotted against resolution (1/d). The cyan line represents the mean radial intensity for lysozyme in LCP medium as a function of 1/d (or resolution in Å on the upper x axis). The green line represents the mean radial intensity for PC in PEO gel medium as a function of 1/d. The error or fluctuation in the radial intensity is quantified using the mean absolute deviation of both media, which is shown as transparent regions. The lines end at different resolution points owing to the different crystal-to-detector distances.

IUCrJ

Volume 4| Part 4| July 2017| Pages 439-454

ISSN: 2052-2525

https://doi.org/10.1107/S205225251700570X

PHYSICS | FELS

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