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Human insulin polymorphism upon ligand binding and pH variation: the case of 4-ethylresorcinol

This study focuses on the effects of the organic ligand 4-ethylresorcinol on the crystal structure of human insulin using powder X-ray crystallography. For this purpose, systematic crystallization experiments have been conducted in the presence of the organic ligand and zinc ions within the pH range...

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Autores principales: Fili, S., Valmas, A., Norrman, M., Schluckebier, G., Beckers, D., Degen, T., Wright, J., Fitch, A., Gozzo, F., Giannopoulou, A. E., Karavassili, F., Margiolaki, I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4547821/
https://www.ncbi.nlm.nih.gov/pubmed/26306195
http://dx.doi.org/10.1107/S2052252515013159
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author Fili, S.
Valmas, A.
Norrman, M.
Schluckebier, G.
Beckers, D.
Degen, T.
Wright, J.
Fitch, A.
Gozzo, F.
Giannopoulou, A. E.
Karavassili, F.
Margiolaki, I.
author_facet Fili, S.
Valmas, A.
Norrman, M.
Schluckebier, G.
Beckers, D.
Degen, T.
Wright, J.
Fitch, A.
Gozzo, F.
Giannopoulou, A. E.
Karavassili, F.
Margiolaki, I.
author_sort Fili, S.
collection PubMed
description This study focuses on the effects of the organic ligand 4-ethylresorcinol on the crystal structure of human insulin using powder X-ray crystallography. For this purpose, systematic crystallization experiments have been conducted in the presence of the organic ligand and zinc ions within the pH range 4.50–8.20, while observing crystallization behaviour around the isoelectric point of insulin. High-throughput crystal screening was performed using a laboratory X-ray diffraction system. The most representative samples were selected for synchrotron X-ray diffraction measurements, which took place at the European Synchrotron Radiation Facility (ESRF) and the Swiss Light Source (SLS). Four different crystalline polymorphs have been identified. Among these, two new phases with monoclinic symmetry have been found, which are targets for the future development of microcrystalline insulin drugs.
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spelling pubmed-45478212015-08-24 Human insulin polymorphism upon ligand binding and pH variation: the case of 4-ethylresorcinol Fili, S. Valmas, A. Norrman, M. Schluckebier, G. Beckers, D. Degen, T. Wright, J. Fitch, A. Gozzo, F. Giannopoulou, A. E. Karavassili, F. Margiolaki, I. IUCrJ Research Papers This study focuses on the effects of the organic ligand 4-ethylresorcinol on the crystal structure of human insulin using powder X-ray crystallography. For this purpose, systematic crystallization experiments have been conducted in the presence of the organic ligand and zinc ions within the pH range 4.50–8.20, while observing crystallization behaviour around the isoelectric point of insulin. High-throughput crystal screening was performed using a laboratory X-ray diffraction system. The most representative samples were selected for synchrotron X-ray diffraction measurements, which took place at the European Synchrotron Radiation Facility (ESRF) and the Swiss Light Source (SLS). Four different crystalline polymorphs have been identified. Among these, two new phases with monoclinic symmetry have been found, which are targets for the future development of microcrystalline insulin drugs. International Union of Crystallography 2015-08-04 /pmc/articles/PMC4547821/ /pubmed/26306195 http://dx.doi.org/10.1107/S2052252515013159 Text en © S. Fili et al. 2015 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 Research Papers
Fili, S.
Valmas, A.
Norrman, M.
Schluckebier, G.
Beckers, D.
Degen, T.
Wright, J.
Fitch, A.
Gozzo, F.
Giannopoulou, A. E.
Karavassili, F.
Margiolaki, I.
Human insulin polymorphism upon ligand binding and pH variation: the case of 4-ethylresorcinol
title Human insulin polymorphism upon ligand binding and pH variation: the case of 4-ethylresorcinol
title_full Human insulin polymorphism upon ligand binding and pH variation: the case of 4-ethylresorcinol
title_fullStr Human insulin polymorphism upon ligand binding and pH variation: the case of 4-ethylresorcinol
title_full_unstemmed Human insulin polymorphism upon ligand binding and pH variation: the case of 4-ethylresorcinol
title_short Human insulin polymorphism upon ligand binding and pH variation: the case of 4-ethylresorcinol
title_sort human insulin polymorphism upon ligand binding and ph variation: the case of 4-ethylresorcinol
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4547821/
https://www.ncbi.nlm.nih.gov/pubmed/26306195
http://dx.doi.org/10.1107/S2052252515013159
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