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 6
The quality of the 2mF_o − DF_c electron-density maps reflects the good quality of the collected data. (a) The A_2AAR protein is shown as a green cartoon and the BRIL fusion protein is shown as a pink cartoon. The ligand ZM241385 (magenta), three cholesterols (orange) and three lipids (yellow and cyan) are shown as stick representations. (b) 2mF_o − DF_c electron-density maps around the residues, shown as sticks, for helices I, II and II.

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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