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Carboplatin binding to histidine
Carboplatin is a second-generation platinum anticancer agent used for the treatment of a variety of cancers. Previous X-ray crystallographic studies of carboplatin binding to histidine (in hen egg-white lysozyme; HEWL) showed the partial conversion of carboplatin to cisplatin owing to the high NaCl...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4157408/ https://www.ncbi.nlm.nih.gov/pubmed/25195881 http://dx.doi.org/10.1107/S2053230X14016161 |
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author | Tanley, Simon W. M. Diederichs, Kay Kroon-Batenburg, Loes M. J. Levy, Colin Schreurs, Antoine M. M. Helliwell, John R. |
author_facet | Tanley, Simon W. M. Diederichs, Kay Kroon-Batenburg, Loes M. J. Levy, Colin Schreurs, Antoine M. M. Helliwell, John R. |
author_sort | Tanley, Simon W. M. |
collection | PubMed |
description | Carboplatin is a second-generation platinum anticancer agent used for the treatment of a variety of cancers. Previous X-ray crystallographic studies of carboplatin binding to histidine (in hen egg-white lysozyme; HEWL) showed the partial conversion of carboplatin to cisplatin owing to the high NaCl concentration used in the crystallization conditions. HEWL co-crystallizations with carboplatin in NaBr conditions have now been carried out to confirm whether carboplatin converts to the bromine form and whether this takes place in a similar way to the partial conversion of carboplatin to cisplatin observed previously in NaCl conditions. Here, it is reported that a partial chemical transformation takes place but to a transplatin form. Thus, to attempt to resolve purely carboplatin binding at histidine, this study utilized co-crystallization of HEWL with carboplatin without NaCl to eliminate the partial chemical conversion of carboplatin. Tetragonal HEWL crystals co-crystallized with carboplatin were successfully obtained in four different conditions, each at a different pH value. The structural results obtained show carboplatin bound to either one or both of the N atoms of His15 of HEWL, and this particular variation was dependent on the concentration of anions in the crystallization mixture and the elapsed time, as well as the pH used. The structural details of the bound carboplatin molecule also differed between them. Overall, the most detailed crystal structure showed the majority of the carboplatin atoms bound to the platinum centre; however, the four-carbon ring structure of the cyclobutanedicarboxylate moiety (CBDC) remained elusive. The potential impact of the results for the administration of carboplatin as an anticancer agent are described. |
format | Online Article Text |
id | pubmed-4157408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-41574082014-10-07 Carboplatin binding to histidine Tanley, Simon W. M. Diederichs, Kay Kroon-Batenburg, Loes M. J. Levy, Colin Schreurs, Antoine M. M. Helliwell, John R. Acta Crystallogr F Struct Biol Commun Structural Communications Carboplatin is a second-generation platinum anticancer agent used for the treatment of a variety of cancers. Previous X-ray crystallographic studies of carboplatin binding to histidine (in hen egg-white lysozyme; HEWL) showed the partial conversion of carboplatin to cisplatin owing to the high NaCl concentration used in the crystallization conditions. HEWL co-crystallizations with carboplatin in NaBr conditions have now been carried out to confirm whether carboplatin converts to the bromine form and whether this takes place in a similar way to the partial conversion of carboplatin to cisplatin observed previously in NaCl conditions. Here, it is reported that a partial chemical transformation takes place but to a transplatin form. Thus, to attempt to resolve purely carboplatin binding at histidine, this study utilized co-crystallization of HEWL with carboplatin without NaCl to eliminate the partial chemical conversion of carboplatin. Tetragonal HEWL crystals co-crystallized with carboplatin were successfully obtained in four different conditions, each at a different pH value. The structural results obtained show carboplatin bound to either one or both of the N atoms of His15 of HEWL, and this particular variation was dependent on the concentration of anions in the crystallization mixture and the elapsed time, as well as the pH used. The structural details of the bound carboplatin molecule also differed between them. Overall, the most detailed crystal structure showed the majority of the carboplatin atoms bound to the platinum centre; however, the four-carbon ring structure of the cyclobutanedicarboxylate moiety (CBDC) remained elusive. The potential impact of the results for the administration of carboplatin as an anticancer agent are described. International Union of Crystallography 2014-08-29 /pmc/articles/PMC4157408/ /pubmed/25195881 http://dx.doi.org/10.1107/S2053230X14016161 Text en © Tanley et al. 2014 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 | Structural Communications Tanley, Simon W. M. Diederichs, Kay Kroon-Batenburg, Loes M. J. Levy, Colin Schreurs, Antoine M. M. Helliwell, John R. Carboplatin binding to histidine |
title | Carboplatin binding to histidine |
title_full | Carboplatin binding to histidine |
title_fullStr | Carboplatin binding to histidine |
title_full_unstemmed | Carboplatin binding to histidine |
title_short | Carboplatin binding to histidine |
title_sort | carboplatin binding to histidine |
topic | Structural Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4157408/ https://www.ncbi.nlm.nih.gov/pubmed/25195881 http://dx.doi.org/10.1107/S2053230X14016161 |
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