<i>In situ</i> counter-diffusion crystallization and long-term crystal preservation in microfluidic fixed targets for serial crystallography
Category
Published on
Type
journal-article
Author
Zhongrui Liu and Kevin Gu and Megan Shelby and Debdyuti Roy and Srinivasan Muniyappan and Marius Schmidt and Sankar Raju Narayanasamy and Matthew Coleman and Matthias Frank and Tonya L. Kuhl
Citation
Liu, Z., Gu, K., Shelby, M., Roy, D., Muniyappan, S., Schmidt, M., Narayanasamy, S. R., Coleman, M., Frank, M., & Kuhl, T. L. (2024). In situ counter-diffusion crystallization and long-term crystal preservation in microfluidic fixed targets for serial crystallography. Journal of Applied Crystallography, 57(5), 1539–1550. https://doi.org/10.1107/s1600576724007544
Abstract
Compared with batch and vapor diffusion methods, counter diffusion can generate larger and higher-quality protein crystals yielding improved diffraction data and higher-resolution structures. Typically, counter-diffusion experiments are conducted in elongated chambers, such as glass capillaries, and the crystals are either directly measured in the capillary or extracted and mounted at the X-ray beamline. Despite the advantages of counter-diffusion protein crystallization, there are few fixed-target devices that utilize counter diffusion for crystallization. In this article, different designs of user-friendly counter-diffusion chambers are presented which can be used to grow large protein crystals in a 2D polymer microfluidic fixed-target chip. Methods for rapid chip fabrication using commercially available thin-film materials such as Mylar, propylene and Kapton are also detailed. Rules of thumb are provided to tune the nucleation and crystal growth to meet users' needs while minimizing sample consumption. These designs provide a reliable approach to forming large crystals and maintaining their hydration for weeks and even months. This allows ample time to grow, select and preserve the best crystal batches before X-ray beam time. Importantly, the fixed-target microfluidic chip has a low background scatter and can be directly used at beamlines without any crystal handling, enabling crystal quality to be preserved. The approach is demonstrated with serial diffraction of photoactive yellow protein, yielding 1.32 Å resolution at room temperature. Fabrication of this standard microfluidic chip with commercially available thin films greatly simplifies fabrication and provides enhanced stability under vacuum. These advances will further broaden microfluidic fixed-target utilization by crystallographers.
DOI
Funding
NSF-STC Biology with X-ray Lasers (NSF-1231306)
