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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
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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 |
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author | Matsumura, Hiroyoshi Sugiyama, Shigeru Hirose, Mika Kakinouchi, Keisuke Maruyama, Mihoko Murai, Ryota Adachi, Hiroaki Takano, Kazufumi Murakami, Satoshi Mori, Yusuke Inoue, Tsuyoshi |
author_facet | Matsumura, Hiroyoshi Sugiyama, Shigeru Hirose, Mika Kakinouchi, Keisuke Maruyama, Mihoko Murai, Ryota Adachi, Hiroaki Takano, Kazufumi Murakami, Satoshi Mori, Yusuke Inoue, Tsuyoshi |
author_sort | Matsumura, Hiroyoshi |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-3004246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30042462010-12-23 Approach for growth of high-quality and large protein crystals Matsumura, Hiroyoshi Sugiyama, Shigeru Hirose, Mika Kakinouchi, Keisuke Maruyama, Mihoko Murai, Ryota Adachi, Hiroaki Takano, Kazufumi Murakami, Satoshi Mori, Yusuke Inoue, Tsuyoshi J Synchrotron Radiat Diffraction Structural Biology 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. International Union of Crystallography 2011-01-01 2010-11-05 /pmc/articles/PMC3004246/ /pubmed/21169683 http://dx.doi.org/10.1107/S090904951003445X Text en © Hiroyoshi Matsumura et al. 2011 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
spellingShingle | Diffraction Structural Biology Matsumura, Hiroyoshi Sugiyama, Shigeru Hirose, Mika Kakinouchi, Keisuke Maruyama, Mihoko Murai, Ryota Adachi, Hiroaki Takano, Kazufumi Murakami, Satoshi Mori, Yusuke Inoue, Tsuyoshi Approach for growth of high-quality and large protein crystals |
title | Approach for growth of high-quality and large protein crystals |
title_full | Approach for growth of high-quality and large protein crystals |
title_fullStr | Approach for growth of high-quality and large protein crystals |
title_full_unstemmed | Approach for growth of high-quality and large protein crystals |
title_short | Approach for growth of high-quality and large protein crystals |
title_sort | approach for growth of high-quality and large protein crystals |
topic | Diffraction Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004246/ https://www.ncbi.nlm.nih.gov/pubmed/21169683 http://dx.doi.org/10.1107/S090904951003445X |
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