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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-...

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Autores principales: Sandlin, Rebecca D., Fong, Kim Y., Stiebler, Renata, Gulka, Christopher P., Nesbitt, Jenny E., Oliveira, Matheus P., Oliveira, Marcus F., Wright, David W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
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.
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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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