SwissMX supports

In close collaboration with the macromolecular crystallography group at PSI and the Institute of Polymer Nanotechnology at PSI/FHNW, we are developing solid supports for protein crystallography at SwissFEL.

SwissMX supports

• developed for serial protein crystallography at XFELs and synchrotrons
• minimized background
• efficient blotting
• solutions for cryo and RT measurements
• optimized for use at the SwissMX instrument at SwissFEL
• adaptable to other formats
• fabrication based on planar technology and additive manufacturing
  (patent application filed)

For more information and test samples
please contact Isabelle Martiel or Celestino Padeste.

Serial femtosecond crystallography (SFX) is a powerful new method for protein structure determination at X-ray free electron lasers (XFELs) and synchrotron X-ray sources [1,2]. It is based on collecting diffraction patterns from large numbers of small protein crystals and allows solving protein structures directly from protein microcrystals, which are too small for standard X-ray techniques. Furthermore, the femtosecond short duration of XFEL pulses allows for dynamic studies of fast structural changes in proteins using pump-probe techniques [3]. To deliver the protein microcrystals at high frequency to the probing X-ray beam, novel protein crystal handling methods such as liquid jet and viscous media injection technologies, as well as the so-called fixed target technology have been developed [4, 5]. In the latter approach, the crystalline sample is deposited on a thin film support, which is mounted on a scanning stage and scanned through the beam, thus sequentially probing the individual microcrystals with the tightly focused x-rays.

The supports are usually fine grid structures or microporous membranes, traditionally produced using silicon/silicon nitride technology, onto which the protein crystal suspension is deposited and separated from the mother liquid through their sieve-function.

We are focusing on the development and fabrication of polymer-based devices, thus taking advantage of the low X-ray absorption and scattering background of polymer materials, absence of X-ray diffraction if using amorphous polymers, the high design flexibility and the potential mass-fabrication at low cost.

References:

[1] S. Boutet et. al., High-resolution protein structure determination by serial femtosecond crystallography. Science 337 (2012) Vol. 6092, pp. 362-364.

[2] T. Weinert et al., Serial millisecond crystallography for routine room-temperature structure determination at synchrotrons, Nat. Commun. 8, 542 (2017).

[3]  V. Paneels et al., Time-resolved structural studies with serial crystallography: A new light on retinal proteins. Structural Dynamics, 2, 041718 (2015)

[4] I. Martiel, H.M. Müller-Werkmeister & A.E. Cohen, Strategies for sample delivery for femtosecond crystallography. Acta Crystallogr. Sect. D. 75, 160–177 (2019).

[5]  M.S. Hunter et al., Fixed-target protein serial microcystallography with an x-ray free electron laser, Sci. Rep. 4, 6026 (2014).