The first step of arsenoplatin-1 aggregation in solution unveiled by solving the crystal structure of its protein adduct
Arsenoplatin-1 (AP-1) is an innovative dual-action anticancer agent that contains a platinum( ii ) center coordinated to an arsenous acid moiety. We found that AP-1 spontaneously aggregates in aqueous solutions generating oligomeric species of increasing length. Afterward, we succeeded in solving th...
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Published in | Dalton transactions : an international journal of inorganic chemistry Vol. 5; no. 1; pp. 68 - 71 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Royal Society of Chemistry
07.01.2021
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Subjects | |
Online Access | Get full text |
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Summary: | Arsenoplatin-1 (AP-1) is an innovative dual-action anticancer agent that contains a platinum(
ii
) center coordinated to an arsenous acid moiety. We found that AP-1 spontaneously aggregates in aqueous solutions generating oligomeric species of increasing length. Afterward, we succeeded in solving the crystal structure of the adduct formed between the model protein lysozyme and an early AP-1 oligomer that turned out to be a trimer. Remarkably, this crystal structure traps an early stage of AP-1 aggregation offering detailed insight into the molecular process of the oligomer's growth.
AP-1 spontaneously aggregates in aqueous solutions. The structure of the adduct formed by an AP-1 trimer with lysozyme offers insight into the process of the oligomer's growth. |
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Bibliography: | 10.1039/D0DT04068A Electronic supplementary information (ESI) available: DETAILS. See DOI ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/d0dt04068a |