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Cell-free protein crystallization for nanocrystal structure determination
In-cell protein crystallization (ICPC) has been investigated as a technique to support the advancement of structural biology because it does not require protein purification and a complicated crystallization process. However, only a few protein structures have been reported because these crystals fo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530169/ https://www.ncbi.nlm.nih.gov/pubmed/36192567 http://dx.doi.org/10.1038/s41598-022-19681-9 |
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author | Abe, Satoshi Tanaka, Junko Kojima, Mariko Kanamaru, Shuji Hirata, Kunio Yamashita, Keitaro Kobayashi, Ayako Ueno, Takafumi |
author_facet | Abe, Satoshi Tanaka, Junko Kojima, Mariko Kanamaru, Shuji Hirata, Kunio Yamashita, Keitaro Kobayashi, Ayako Ueno, Takafumi |
author_sort | Abe, Satoshi |
collection | PubMed |
description | In-cell protein crystallization (ICPC) has been investigated as a technique to support the advancement of structural biology because it does not require protein purification and a complicated crystallization process. However, only a few protein structures have been reported because these crystals formed incidentally in living cells and are insufficient in size and quality for structure analysis. Here, we have developed a cell-free protein crystallization (CFPC) method, which involves direct protein crystallization using cell-free protein synthesis. We have succeeded in crystallization and structure determination of nano-sized polyhedra crystal (PhC) at a high resolution of 1.80 Å. Furthermore, nanocrystals were synthesized at a reaction scale of only 20 μL using the dialysis method, enabling structural analysis at a resolution of 1.95 Å. To further demonstrate the potential of CFPC, we attempted to determine the structure of crystalline inclusion protein A (CipA), whose structure had not yet been determined. We added chemical reagents as a twinning inhibitor to the CFPC solution, which enabled us to determine the structure of CipA at 2.11 Å resolution. This technology greatly expands the high-throughput structure determination method of unstable, low-yield, fusion, and substrate-biding proteins that have been difficult to analyze with conventional methods. |
format | Online Article Text |
id | pubmed-9530169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95301692022-10-05 Cell-free protein crystallization for nanocrystal structure determination Abe, Satoshi Tanaka, Junko Kojima, Mariko Kanamaru, Shuji Hirata, Kunio Yamashita, Keitaro Kobayashi, Ayako Ueno, Takafumi Sci Rep Article In-cell protein crystallization (ICPC) has been investigated as a technique to support the advancement of structural biology because it does not require protein purification and a complicated crystallization process. However, only a few protein structures have been reported because these crystals formed incidentally in living cells and are insufficient in size and quality for structure analysis. Here, we have developed a cell-free protein crystallization (CFPC) method, which involves direct protein crystallization using cell-free protein synthesis. We have succeeded in crystallization and structure determination of nano-sized polyhedra crystal (PhC) at a high resolution of 1.80 Å. Furthermore, nanocrystals were synthesized at a reaction scale of only 20 μL using the dialysis method, enabling structural analysis at a resolution of 1.95 Å. To further demonstrate the potential of CFPC, we attempted to determine the structure of crystalline inclusion protein A (CipA), whose structure had not yet been determined. We added chemical reagents as a twinning inhibitor to the CFPC solution, which enabled us to determine the structure of CipA at 2.11 Å resolution. This technology greatly expands the high-throughput structure determination method of unstable, low-yield, fusion, and substrate-biding proteins that have been difficult to analyze with conventional methods. Nature Publishing Group UK 2022-10-03 /pmc/articles/PMC9530169/ /pubmed/36192567 http://dx.doi.org/10.1038/s41598-022-19681-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Abe, Satoshi Tanaka, Junko Kojima, Mariko Kanamaru, Shuji Hirata, Kunio Yamashita, Keitaro Kobayashi, Ayako Ueno, Takafumi Cell-free protein crystallization for nanocrystal structure determination |
title | Cell-free protein crystallization for nanocrystal structure determination |
title_full | Cell-free protein crystallization for nanocrystal structure determination |
title_fullStr | Cell-free protein crystallization for nanocrystal structure determination |
title_full_unstemmed | Cell-free protein crystallization for nanocrystal structure determination |
title_short | Cell-free protein crystallization for nanocrystal structure determination |
title_sort | cell-free protein crystallization for nanocrystal structure determination |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530169/ https://www.ncbi.nlm.nih.gov/pubmed/36192567 http://dx.doi.org/10.1038/s41598-022-19681-9 |
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