Self-Assembled Nanostructures of Peptide Amphiphiles: Charge Regulation by Size Regulation
- Autores
- Zaldivar, Gervasio; Vemulapalli, Sridhar; Udumula, Venkatareddy; Conda Sheridan, Martin; Tagliazucchi, Mario Eugenio
- Año de publicación
- 2019
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Self-assembled nanostructures of peptide amphiphiles (PAs) with molecular structures C16K2 and C16K3 (where C indicates the number of carbon atoms in the alkyl chain and K is the lysine in the head group) were studied by a combination of theoretical modeling, transmission electron and atomic force microscopes, and acid-base titration experiments. The supramolecular morphology of the PAs (micelles, fibers, or lamellas) was dependent on the pH and ionic strength of the solution. Theoretical modeling was performed using a molecular theory that allows determining the equilibrium morphology, the size, and the charge of the soft nanoassemblies as a function of the molecular structure of the PA, and the pH and salt concentration of the solution. Theoretical predictions showed good agreement with experimental data for the pH-dependent morphology and size of the nanoassemblies and their apparent pKa's. Two interesting effects associated with charge regulation mechanisms were found: first, ionic strength plays a dual role in the modulation of the electrostatic interactions in the system, which leads to complex dependencies of the aggregation numbers with salt concentration; second, the aggregation number of the nanostructures decreases upon increasing the charge per PA. The second mechanism, charge regulation by size regulation, tunes the net charge of the assemblies to decrease the electrostatic repulsions. A remarkable consequence of this behavior is that adding an extra lysine residue to the charged region of the PAs can lead to an unexpected decrease in the total charge of the micelles.
Fil: Zaldivar, Gervasio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Vemulapalli, Sridhar. University Of Nebraska Medical Center; Estados Unidos
Fil: Udumula, Venkatareddy. University Of Nebraska Medical Center; Estados Unidos
Fil: Conda Sheridan, Martin. University Of Nebraska Medical Center; Estados Unidos
Fil: Tagliazucchi, Mario Eugenio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina - Materia
-
charge regultation
molecular theory
micelles
fiber - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/123594
Ver los metadatos del registro completo
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Self-Assembled Nanostructures of Peptide Amphiphiles: Charge Regulation by Size RegulationZaldivar, GervasioVemulapalli, SridharUdumula, VenkatareddyConda Sheridan, MartinTagliazucchi, Mario Eugeniocharge regultationmolecular theorymicellesfiberhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1Self-assembled nanostructures of peptide amphiphiles (PAs) with molecular structures C16K2 and C16K3 (where C indicates the number of carbon atoms in the alkyl chain and K is the lysine in the head group) were studied by a combination of theoretical modeling, transmission electron and atomic force microscopes, and acid-base titration experiments. The supramolecular morphology of the PAs (micelles, fibers, or lamellas) was dependent on the pH and ionic strength of the solution. Theoretical modeling was performed using a molecular theory that allows determining the equilibrium morphology, the size, and the charge of the soft nanoassemblies as a function of the molecular structure of the PA, and the pH and salt concentration of the solution. Theoretical predictions showed good agreement with experimental data for the pH-dependent morphology and size of the nanoassemblies and their apparent pKa's. Two interesting effects associated with charge regulation mechanisms were found: first, ionic strength plays a dual role in the modulation of the electrostatic interactions in the system, which leads to complex dependencies of the aggregation numbers with salt concentration; second, the aggregation number of the nanostructures decreases upon increasing the charge per PA. The second mechanism, charge regulation by size regulation, tunes the net charge of the assemblies to decrease the electrostatic repulsions. A remarkable consequence of this behavior is that adding an extra lysine residue to the charged region of the PAs can lead to an unexpected decrease in the total charge of the micelles.Fil: Zaldivar, Gervasio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; ArgentinaFil: Vemulapalli, Sridhar. University Of Nebraska Medical Center; Estados UnidosFil: Udumula, Venkatareddy. University Of Nebraska Medical Center; Estados UnidosFil: Conda Sheridan, Martin. University Of Nebraska Medical Center; Estados UnidosFil: Tagliazucchi, Mario Eugenio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; ArgentinaAmerican Chemical Society2019-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/123594Zaldivar, Gervasio; Vemulapalli, Sridhar; Udumula, Venkatareddy; Conda Sheridan, Martin; Tagliazucchi, Mario Eugenio; Self-Assembled Nanostructures of Peptide Amphiphiles: Charge Regulation by Size Regulation; American Chemical Society; Journal of Physical Chemistry C; 123; 28; 6-2019; 17606-176151932-7447CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1021/acs.jpcc.9b04280info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-22T11:46:02Zoai:ri.conicet.gov.ar:11336/123594instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-22 11:46:03.276CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Self-Assembled Nanostructures of Peptide Amphiphiles: Charge Regulation by Size Regulation |
| title |
Self-Assembled Nanostructures of Peptide Amphiphiles: Charge Regulation by Size Regulation |
| spellingShingle |
Self-Assembled Nanostructures of Peptide Amphiphiles: Charge Regulation by Size Regulation Zaldivar, Gervasio charge regultation molecular theory micelles fiber |
| title_short |
Self-Assembled Nanostructures of Peptide Amphiphiles: Charge Regulation by Size Regulation |
| title_full |
Self-Assembled Nanostructures of Peptide Amphiphiles: Charge Regulation by Size Regulation |
| title_fullStr |
Self-Assembled Nanostructures of Peptide Amphiphiles: Charge Regulation by Size Regulation |
| title_full_unstemmed |
Self-Assembled Nanostructures of Peptide Amphiphiles: Charge Regulation by Size Regulation |
| title_sort |
Self-Assembled Nanostructures of Peptide Amphiphiles: Charge Regulation by Size Regulation |
| dc.creator.none.fl_str_mv |
Zaldivar, Gervasio Vemulapalli, Sridhar Udumula, Venkatareddy Conda Sheridan, Martin Tagliazucchi, Mario Eugenio |
| author |
Zaldivar, Gervasio |
| author_facet |
Zaldivar, Gervasio Vemulapalli, Sridhar Udumula, Venkatareddy Conda Sheridan, Martin Tagliazucchi, Mario Eugenio |
| author_role |
author |
| author2 |
Vemulapalli, Sridhar Udumula, Venkatareddy Conda Sheridan, Martin Tagliazucchi, Mario Eugenio |
| author2_role |
author author author author |
| dc.subject.none.fl_str_mv |
charge regultation molecular theory micelles fiber |
| topic |
charge regultation molecular theory micelles fiber |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
| dc.description.none.fl_txt_mv |
Self-assembled nanostructures of peptide amphiphiles (PAs) with molecular structures C16K2 and C16K3 (where C indicates the number of carbon atoms in the alkyl chain and K is the lysine in the head group) were studied by a combination of theoretical modeling, transmission electron and atomic force microscopes, and acid-base titration experiments. The supramolecular morphology of the PAs (micelles, fibers, or lamellas) was dependent on the pH and ionic strength of the solution. Theoretical modeling was performed using a molecular theory that allows determining the equilibrium morphology, the size, and the charge of the soft nanoassemblies as a function of the molecular structure of the PA, and the pH and salt concentration of the solution. Theoretical predictions showed good agreement with experimental data for the pH-dependent morphology and size of the nanoassemblies and their apparent pKa's. Two interesting effects associated with charge regulation mechanisms were found: first, ionic strength plays a dual role in the modulation of the electrostatic interactions in the system, which leads to complex dependencies of the aggregation numbers with salt concentration; second, the aggregation number of the nanostructures decreases upon increasing the charge per PA. The second mechanism, charge regulation by size regulation, tunes the net charge of the assemblies to decrease the electrostatic repulsions. A remarkable consequence of this behavior is that adding an extra lysine residue to the charged region of the PAs can lead to an unexpected decrease in the total charge of the micelles. Fil: Zaldivar, Gervasio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina Fil: Vemulapalli, Sridhar. University Of Nebraska Medical Center; Estados Unidos Fil: Udumula, Venkatareddy. University Of Nebraska Medical Center; Estados Unidos Fil: Conda Sheridan, Martin. University Of Nebraska Medical Center; Estados Unidos Fil: Tagliazucchi, Mario Eugenio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina |
| description |
Self-assembled nanostructures of peptide amphiphiles (PAs) with molecular structures C16K2 and C16K3 (where C indicates the number of carbon atoms in the alkyl chain and K is the lysine in the head group) were studied by a combination of theoretical modeling, transmission electron and atomic force microscopes, and acid-base titration experiments. The supramolecular morphology of the PAs (micelles, fibers, or lamellas) was dependent on the pH and ionic strength of the solution. Theoretical modeling was performed using a molecular theory that allows determining the equilibrium morphology, the size, and the charge of the soft nanoassemblies as a function of the molecular structure of the PA, and the pH and salt concentration of the solution. Theoretical predictions showed good agreement with experimental data for the pH-dependent morphology and size of the nanoassemblies and their apparent pKa's. Two interesting effects associated with charge regulation mechanisms were found: first, ionic strength plays a dual role in the modulation of the electrostatic interactions in the system, which leads to complex dependencies of the aggregation numbers with salt concentration; second, the aggregation number of the nanostructures decreases upon increasing the charge per PA. The second mechanism, charge regulation by size regulation, tunes the net charge of the assemblies to decrease the electrostatic repulsions. A remarkable consequence of this behavior is that adding an extra lysine residue to the charged region of the PAs can lead to an unexpected decrease in the total charge of the micelles. |
| publishDate |
2019 |
| dc.date.none.fl_str_mv |
2019-06 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
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publishedVersion |
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http://hdl.handle.net/11336/123594 Zaldivar, Gervasio; Vemulapalli, Sridhar; Udumula, Venkatareddy; Conda Sheridan, Martin; Tagliazucchi, Mario Eugenio; Self-Assembled Nanostructures of Peptide Amphiphiles: Charge Regulation by Size Regulation; American Chemical Society; Journal of Physical Chemistry C; 123; 28; 6-2019; 17606-17615 1932-7447 CONICET Digital CONICET |
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http://hdl.handle.net/11336/123594 |
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Zaldivar, Gervasio; Vemulapalli, Sridhar; Udumula, Venkatareddy; Conda Sheridan, Martin; Tagliazucchi, Mario Eugenio; Self-Assembled Nanostructures of Peptide Amphiphiles: Charge Regulation by Size Regulation; American Chemical Society; Journal of Physical Chemistry C; 123; 28; 6-2019; 17606-17615 1932-7447 CONICET Digital CONICET |
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eng |
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eng |
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info:eu-repo/semantics/altIdentifier/doi/10.1021/acs.jpcc.9b04280 |
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American Chemical Society |
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American Chemical Society |
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