4.7 Article

Plug-and-play polymer microfluidic chips for hydrated, room temperature, fixed-target serial crystallography

期刊

LAB ON A CHIP
卷 21, 期 24, 页码 4831-4845

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1lc00810b

关键词

-

资金

  1. U.S. DOE by LLNL [DE-AC52-07NA27344]
  2. National Science Foundation (NSF) BioXFEL STC Grant [1231306]
  3. NIH [R01GM117342, U19 AI144184]
  4. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-76SF00515]
  5. DOE Office of Biological and Environmental Research
  6. National Institutes of Health, National Institute of General Medical Sciences [P30GM133894]

向作者/读者索取更多资源

The development of versatile, inexpensive, and robust polymer microfluidic chips for serial X-ray crystallography allows for efficient sample delivery and measurements at both synchrotrons and X-ray free electron lasers. The chips offer advantages such as low sample consumption, minimal background scattering, and precise control over sample flow, making them suitable for a wide range of protein crystallography experiments.
The practice of serial X-ray crystallography (SX) depends on efficient, continuous delivery of hydrated protein crystals while minimizing background scattering. Of the two major types of sample delivery devices, fixed-target devices offer several advantages over widely adopted jet injectors, including: lower sample consumption, clog-free delivery, and the ability to control on-chip crystal density to improve hit rates. Here we present our development of versatile, inexpensive, and robust polymer microfluidic chips for routine and reliable room temperature serial measurements at both synchrotrons and X-ray free electron lasers (XFELs). Our design includes highly X-ray-transparent enclosing thin film layers tuned to minimize scatter background, adaptable sample flow layers tuned to match crystal size, and a large sample area compatible with both raster scanning and rotation based serial data collection. The optically transparent chips can be used both for in situ protein crystallization (to eliminate crystal handling) or crystal slurry loading, with prepared samples stable for weeks in a humidified environment and for several hours in ambient conditions. Serial oscillation crystallography, using a multi-crystal rotational data collection approach, at a microfocus synchrotron beamline (SSRL, beamline 12-1) was used to benchmark the performance of the chips. High-resolution structures (1.3-2.7 angstrom) were collected from five different proteins - hen egg white lysozyme, thaumatin, bovine liver catalase, concanavalin-A (type VI), and SARS-CoV-2 nonstructural protein NSP5. Overall, our modular fabrication approach enables precise control over the cross-section of materials in the X-ray beam path and facilitates chip adaption to different sample and beamline requirements for user-friendly, straightforward diffraction measurements at room temperature.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据