Samples were prepared according to standardized approaches for synchrotron SAXS data collection
44 (link).
The RBD from Spike glycoprotein, SARS-CoV-2, was expressed in HEK293-F cells and purified as previously described
37 (link). Purified RBD was stored frozen (−80 °C) and dialyzed overnight into a PBS buffer before measurement.
Standard proteins were purchased from Sigma (Darmstadt, Germany):
Bovine Thyroglobulin (Sigma-T1001),
Equine Apoferritin (Sigma-A3660), and
Bovine Serum Albumin (Sigma-A7030). Each standard was dissolved in a PBS buffer and filtered using an Ultrafree®-MC spin-filter device (12,000×
g, 4 min.) prior to measurement.
Blanchet C.E., Round A., Mertens H.D., Ayyer K., Graewert M., Awel S., Franke D., Dörner K., Bajt S., Bean R., Custódio T.F., de Wijn R., Juncheng E., Henkel A., Gruzinov A., Jeffries C.M., Kim Y., Kirkwood H., Kloos M., Knoška J., Koliyadu J., Letrun R., Löw C., Makroczyova J., Mall A., Meijers R., Pena Murillo G.E., Oberthür D., Round E., Seuring C., Sikorski M., Vagovic P., Valerio J., Wollweber T., Zhuang Y., Schulz J., Haas H., Chapman H.N., Mancuso A.P, & Svergun D. (2023). Form factor determination of biological molecules with X-ray free electron laser small-angle scattering (XFEL-SAS). Communications Biology, 6, 1057.