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Detergent-Mediated Formation of β-Hematin: Heme Crystallization Promoted by Detergents Implicates Nanostructure Formation for Use as a Biological Mimic
[Image: see text] Hemozoin is a unique biomineral that results from the sequestration of toxic free heme liberated as a consequence of hemoglobin degradation in the malaria parasite. Synthetic neutral lipid droplets (SNLDs) and phospholipids were previously shown to support the rapid formation of β-...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4860678/ https://www.ncbi.nlm.nih.gov/pubmed/27175104 http://dx.doi.org/10.1021/acs.cgd.5b01580 |
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author | Sandlin, Rebecca D. Fong, Kim Y. Stiebler, Renata Gulka, Christopher P. Nesbitt, Jenny E. Oliveira, Matheus P. Oliveira, Marcus F. Wright, David W. |
author_facet | Sandlin, Rebecca D. Fong, Kim Y. Stiebler, Renata Gulka, Christopher P. Nesbitt, Jenny E. Oliveira, Matheus P. Oliveira, Marcus F. Wright, David W. |
author_sort | Sandlin, Rebecca D. |
collection | PubMed |
description | [Image: see text] Hemozoin is a unique biomineral that results from the sequestration of toxic free heme liberated as a consequence of hemoglobin degradation in the malaria parasite. Synthetic neutral lipid droplets (SNLDs) and phospholipids were previously shown to support the rapid formation of β-hematin, abiological hemozoin, under physiologically relevant pH and temperature, though the mechanism by which heme crystallization occurs remains unclear. Detergents are particularly interesting as a template because they are amphiphilic molecules that spontaneously organize into nanostructures and have been previously shown to mediate β-hematin formation. Here, 11 detergents were investigated to elucidate the physicochemical properties that best recapitulate crystal formation in the parasite. A strong correlation between the detergent’s molecular structure and the corresponding kinetics of β-hematin formation was observed, where higher molecular weight polar chains promoted faster reactions. The larger hydrophilic chains correlated to the detergent’s ability to rapidly sequester heme into the lipophilic core, allowing for crystal nucleation to occur. The data presented here suggest that detergent nanostructures promote β-hematin formation in a similar manner to SNLDs and phospholipids. Through understanding mediator properties that promote optimal crystal formation, we are able to establish an in vitro assay to probe this drug target pathway. |
format | Online Article Text |
id | pubmed-4860678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-48606782016-05-10 Detergent-Mediated Formation of β-Hematin: Heme Crystallization Promoted by Detergents Implicates Nanostructure Formation for Use as a Biological Mimic Sandlin, Rebecca D. Fong, Kim Y. Stiebler, Renata Gulka, Christopher P. Nesbitt, Jenny E. Oliveira, Matheus P. Oliveira, Marcus F. Wright, David W. Cryst Growth Des [Image: see text] Hemozoin is a unique biomineral that results from the sequestration of toxic free heme liberated as a consequence of hemoglobin degradation in the malaria parasite. Synthetic neutral lipid droplets (SNLDs) and phospholipids were previously shown to support the rapid formation of β-hematin, abiological hemozoin, under physiologically relevant pH and temperature, though the mechanism by which heme crystallization occurs remains unclear. Detergents are particularly interesting as a template because they are amphiphilic molecules that spontaneously organize into nanostructures and have been previously shown to mediate β-hematin formation. Here, 11 detergents were investigated to elucidate the physicochemical properties that best recapitulate crystal formation in the parasite. A strong correlation between the detergent’s molecular structure and the corresponding kinetics of β-hematin formation was observed, where higher molecular weight polar chains promoted faster reactions. The larger hydrophilic chains correlated to the detergent’s ability to rapidly sequester heme into the lipophilic core, allowing for crystal nucleation to occur. The data presented here suggest that detergent nanostructures promote β-hematin formation in a similar manner to SNLDs and phospholipids. Through understanding mediator properties that promote optimal crystal formation, we are able to establish an in vitro assay to probe this drug target pathway. American Chemical Society 2016-04-11 2016-05-04 /pmc/articles/PMC4860678/ /pubmed/27175104 http://dx.doi.org/10.1021/acs.cgd.5b01580 Text en Copyright © 2016 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Sandlin, Rebecca D. Fong, Kim Y. Stiebler, Renata Gulka, Christopher P. Nesbitt, Jenny E. Oliveira, Matheus P. Oliveira, Marcus F. Wright, David W. Detergent-Mediated Formation of β-Hematin: Heme Crystallization Promoted by Detergents Implicates Nanostructure Formation for Use as a Biological Mimic |
title | Detergent-Mediated Formation of β-Hematin:
Heme Crystallization Promoted by Detergents Implicates Nanostructure
Formation for Use as a Biological Mimic |
title_full | Detergent-Mediated Formation of β-Hematin:
Heme Crystallization Promoted by Detergents Implicates Nanostructure
Formation for Use as a Biological Mimic |
title_fullStr | Detergent-Mediated Formation of β-Hematin:
Heme Crystallization Promoted by Detergents Implicates Nanostructure
Formation for Use as a Biological Mimic |
title_full_unstemmed | Detergent-Mediated Formation of β-Hematin:
Heme Crystallization Promoted by Detergents Implicates Nanostructure
Formation for Use as a Biological Mimic |
title_short | Detergent-Mediated Formation of β-Hematin:
Heme Crystallization Promoted by Detergents Implicates Nanostructure
Formation for Use as a Biological Mimic |
title_sort | detergent-mediated formation of β-hematin:
heme crystallization promoted by detergents implicates nanostructure
formation for use as a biological mimic |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4860678/ https://www.ncbi.nlm.nih.gov/pubmed/27175104 http://dx.doi.org/10.1021/acs.cgd.5b01580 |
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