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Approach for growth of high-quality and large protein crystals

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...

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Detalles Bibliográficos
Autores principales: Matsumura, Hiroyoshi, Sugiyama, Shigeru, Hirose, Mika, Kakinouchi, Keisuke, Maruyama, Mihoko, Murai, Ryota, Adachi, Hiroaki, Takano, Kazufumi, Murakami, Satoshi, Mori, Yusuke, Inoue, Tsuyoshi
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004246/
https://www.ncbi.nlm.nih.gov/pubmed/21169683
http://dx.doi.org/10.1107/S090904951003445X
Descripción
Sumario: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.