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Exploring Carbon Nanomaterial Diversity for Nucleation of Protein Crystals
Controlling crystal nucleation is a crucial step in obtaining high quality protein crystals for structure determination by X-ray crystallography. Carbon nanomaterials (CNMs) including carbon nanotubes, graphene oxide, and carbon black provide a range of surface topographies, porosities and length sc...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4740738/ https://www.ncbi.nlm.nih.gov/pubmed/26843366 http://dx.doi.org/10.1038/srep20053 |
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author | Govada, Lata Leese, Hannah S. Saridakis, Emmanuel Kassen, Sean Chain, Benny Khurshid, Sahir Menzel, Robert Hu, Sheng Shaffer, Milo S. P. Chayen, Naomi E. |
author_facet | Govada, Lata Leese, Hannah S. Saridakis, Emmanuel Kassen, Sean Chain, Benny Khurshid, Sahir Menzel, Robert Hu, Sheng Shaffer, Milo S. P. Chayen, Naomi E. |
author_sort | Govada, Lata |
collection | PubMed |
description | Controlling crystal nucleation is a crucial step in obtaining high quality protein crystals for structure determination by X-ray crystallography. Carbon nanomaterials (CNMs) including carbon nanotubes, graphene oxide, and carbon black provide a range of surface topographies, porosities and length scales; functionalisation with two different approaches, gas phase radical grafting and liquid phase reductive grafting, provide routes to a range of oligomer functionalised products. These grafted materials, combined with a range of controls, were used in a large-scale assessment of the effectiveness for protein crystal nucleation of 20 different carbon nanomaterials on five proteins. This study has allowed a direct comparison of the key characteristics of carbon-based nucleants: appropriate surface chemistry, porosity and/or roughness are required. The most effective solid system tested in this study, carbon black nanoparticles functionalised with poly(ethylene glycol) methyl ether of mean molecular weight 5000, provides a novel highly effective nucleant, that was able to induce crystal nucleation of four out of the five proteins tested at metastable conditions. |
format | Online Article Text |
id | pubmed-4740738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47407382016-02-09 Exploring Carbon Nanomaterial Diversity for Nucleation of Protein Crystals Govada, Lata Leese, Hannah S. Saridakis, Emmanuel Kassen, Sean Chain, Benny Khurshid, Sahir Menzel, Robert Hu, Sheng Shaffer, Milo S. P. Chayen, Naomi E. Sci Rep Article Controlling crystal nucleation is a crucial step in obtaining high quality protein crystals for structure determination by X-ray crystallography. Carbon nanomaterials (CNMs) including carbon nanotubes, graphene oxide, and carbon black provide a range of surface topographies, porosities and length scales; functionalisation with two different approaches, gas phase radical grafting and liquid phase reductive grafting, provide routes to a range of oligomer functionalised products. These grafted materials, combined with a range of controls, were used in a large-scale assessment of the effectiveness for protein crystal nucleation of 20 different carbon nanomaterials on five proteins. This study has allowed a direct comparison of the key characteristics of carbon-based nucleants: appropriate surface chemistry, porosity and/or roughness are required. The most effective solid system tested in this study, carbon black nanoparticles functionalised with poly(ethylene glycol) methyl ether of mean molecular weight 5000, provides a novel highly effective nucleant, that was able to induce crystal nucleation of four out of the five proteins tested at metastable conditions. Nature Publishing Group 2016-02-04 /pmc/articles/PMC4740738/ /pubmed/26843366 http://dx.doi.org/10.1038/srep20053 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Govada, Lata Leese, Hannah S. Saridakis, Emmanuel Kassen, Sean Chain, Benny Khurshid, Sahir Menzel, Robert Hu, Sheng Shaffer, Milo S. P. Chayen, Naomi E. Exploring Carbon Nanomaterial Diversity for Nucleation of Protein Crystals |
title | Exploring Carbon Nanomaterial Diversity for Nucleation of Protein Crystals |
title_full | Exploring Carbon Nanomaterial Diversity for Nucleation of Protein Crystals |
title_fullStr | Exploring Carbon Nanomaterial Diversity for Nucleation of Protein Crystals |
title_full_unstemmed | Exploring Carbon Nanomaterial Diversity for Nucleation of Protein Crystals |
title_short | Exploring Carbon Nanomaterial Diversity for Nucleation of Protein Crystals |
title_sort | exploring carbon nanomaterial diversity for nucleation of protein crystals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4740738/ https://www.ncbi.nlm.nih.gov/pubmed/26843366 http://dx.doi.org/10.1038/srep20053 |
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