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A novel sample delivery system based on circular motion for in situ serial synchrotron crystallography
Feng-Zhu Zhao1, Bo Sun2, Li Yu3
1School of Life Sciences, Northwestern Polytechnical University, Xi'an, China. yindc@nwpu.edu.cn.
Lab on a Chip
|September 23, 2020
Summary
This study introduces a novel microfluidic rotating-target device for serial crystallography, improving sample delivery efficiency. The device uses circular motion for sample delivery, enabling successful protein structure determination at a synchrotron facility.
Area of Science:
- Crystallography
- Biophysics
- Materials Science
Background:
- Sample delivery is a critical bottleneck in serial crystallography.
- Existing methods primarily use linear motion for sample delivery.
- Improving sample delivery performance and efficiency is an ongoing challenge.
Purpose of the Study:
- To develop and validate a novel microfluidic rotating-target device for serial crystallography.
- To demonstrate the feasibility of using circular motion for sample delivery in crystallography.
- To assess the device's performance at a synchrotron radiation facility.
Main Methods:
- Design of a microfluidic rotating-target sample delivery device with a microfluidic sample plate and motion control system.
- Implementation of circular motion for sample delivery.
- In situ serial crystallography experiments using lysozyme and proteinase K at the Shanghai Synchrotron Radiation Facility.
Main Results:
- The microfluidic rotating-target device demonstrated a wide adjustable delivery speed range, low background noise, and low sample consumption.
- The device is fully compatible with synchrotron radiation facilities.
- Successful protein structure determination was achieved using data from the device.
Conclusions:
- Circular motion is a viable and effective alternative for sample delivery in serial crystallography.
- The microfluidic rotating-target device offers significant advantages for serial crystallography applications.
- This novel approach enhances the efficiency and performance of serial crystallography experiments.

