Fixed-Targets for Serial Protein Crystallography at SwissFEL

Presented During:

07/30/2022: 5:30 PM - 7:30 PM
Portland Marriott Downtown Waterfront  


2022: 72nd ACA Annual Meeting

Session Type:


Presenting Author :

Melissa Carrillo  

Additional Author(s):

John Beale  
Paul Scherrer institut
Celestino Padeste  
Paul Scherrer Institute

Abstract Body:

X-ray free electron lasers (XFELs) have enabled the overcoming of limitations of classical crystallography by outrunning radiation damage with their highly coherent and brilliant femtosecond pulses. As a consequence of crystal destruction, large numbers of new crystals must be introduced sequentially to the beam, establishing methods such as serial femtosecond crystallography (SFX) and time-resolved serial femtosecond crystallography (TR-SFX) [1]. Both SFX and TR-SFX have provided new modes of structural biology. However, the constant need to refresh crystals in the beam path is a constant challenge and improvements to sample delivery can greatly improve experimental outcomes.

Fixed-target sample delivery methods allow for a reduction of sample consumption and optimization of sample density without issues such as clogging. Fixed-targets also lend themselves to high throughput technologies and an increased ability to locate and position crystals. Silicon wafers are the most common fixed-target and offer an inert support for the immobilized crystals and a precise aperture array for rapid alignment strategies [2]. However, the silicon wafers are brittle, expensive and can give strong Si(111) reflections in misaligned [3, 4].

Here we present preliminary data on the fabrication of polymer-based fixed-targets being developed for TR-SFX at SwissMX, the new end station dedicated to fixed-target SFX at SwissFEL, Switzerland's X-ray free-electron laser. The polymer-based film provides low x-ray absorption and scattering background, high design flexibility and the potential mass-fabrication at low cost. Using silicon microfabrication and polymer replication technologies, we have designed inverted pyramidal shaped wells in membranes ranging from 25-50 µm in thickness. This design enables single crystals to funnel into predefined positions, optimizing the hit-rate of the probing X-ray beam.

[1] Chapman, Henry N., et al. "Femtosecond X-ray protein nanocrystallography." Nature 470.7332 (2011): 73-77.
[2] Sherrell, Darren A., et al. "A modular and compact portable mini-endstation for high-precision, high-speed fixed target serial crystallography at FEL and synchrotron sources." Journal of synchrotron radiation 22.6 (2015): 1372-1378.
[3] Cheng, Robert KY. "Towards an optimal sample delivery method for serial crystallography at XFEL." Crystals 10.3 (2020): 215.
[4] Martiel, Isabelle, Henrike M. Müller-Werkmeister, and Aina E. Cohen. "Strategies for sample delivery for femtosecond crystallography." Acta Crystallographica Section D: Structural Biology 75.2 (2019): 160-177.

Additional Information - Poster (2022)

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4.2.1 Advances in xfel and synchrotron serial crystallography, Herbert J. Bernstein

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Journal on Structural Dynamics