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Approach for growth of high-quality and large protein crystals
Authors:Matsumura Hiroyoshi  Sugiyama Shigeru  Hirose Mika  Kakinouchi Keisuke  Maruyama Mihoko  Murai Ryota  Adachi Hiroaki  Takano Kazufumi  Murakami Satoshi  Mori Yusuke  Inoue Tsuyoshi
Affiliation:Graduate School of Engineering, Osaka University, Suita, Osaka 565-0871, Japan. matsumura@chem.eng.osaka-u.ac.jp
Abstract:
Three crystallization methods for growing large high-quality protein crystals, i.e. crystallization in the presence of a semi-solid agarose gel, top-seeded solution growth (TSSG) and a large-scale hanging-drop method, have previously been presented. In this study the effectiveness of crystallization in the presence of a semi-solid agarose gel has been further evaluated by crystallizing additional proteins in the presence of 2.0% (w/v) agarose gel, resulting in complete gelification with high mechanical strength. In TSSG the seed crystals are hung by a seed holder protruding from the top of the growth vessel to prevent polycrystallization. In the large-scale hanging-drop method, a cut pipette tip was used to maintain large-scale droplets consisting of protein-precipitant solution. Here a novel crystallization method that combines TSSG and the large-scale hanging-drop method is reported. A large and single crystal of lysozyme was obtained by this method.
Keywords:
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