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通过液滴微流控系统控制一种蛋白质晶体生长。

Controlling one protein crystal growth by droplet-based microfluidic system.

机构信息

Measurement Solution Research Center, National Institute of Advanced Industrial Science and Technology, Tosu, Saga 841-0052, Japan.

出版信息

J Biochem. 2013 Apr;153(4):339-46. doi: 10.1093/jb/mvt001. Epub 2013 Jan 10.

Abstract

The preparation of a single crystal is important for a detailed understanding of the structure of protein. However, the preparation of a suitable crystal for X-ray diffraction is often a drawback due to the complexity of the protein molecules and the limited fundamental understanding of the protein crystallization mechanism. In this study, we studied the crystallization mechanism in droplet that was prepared by the microfluidic chip. We found that the mechanism of crystal growth in droplet is different from that by a conventional microbatch method. One crystal was grown in one droplet by controlling droplet shape and droplet volume. In addition, the surface area in droplet affected the size of the obtained protein crystal and the number of crystal(s). The growth of the (110) and (101) faces of tetragonal crystal could be determined by studying one crystal formed within one droplet, indicating that the observation and evaluation of one crystal growth kinetics is easily carried out compared with the conventional method.

摘要

制备单晶对于深入了解蛋白质结构非常重要。然而,由于蛋白质分子的复杂性以及对蛋白质结晶机制的有限理解,通常由于制备合适的用于 X 射线衍射的晶体而成为一个难题。在这项研究中,我们研究了在微流控芯片制备的液滴中的结晶机制。我们发现液滴中晶体生长的机制与传统的微批量方法不同。通过控制液滴形状和液滴体积,在一个液滴中生长出一个单晶。此外,液滴中的表面积影响得到的蛋白质晶体的大小和数量。通过研究在一个液滴中形成的一个单晶,可以确定四方晶的(110)和(101)面的生长,表明与传统方法相比,更容易进行单晶生长动力学的观察和评估。

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