Ryan Lloyd, Abdullah Ba Salem, Noah Gallant and Jean Duhamel*,
{"title":"DNA与芘标记表面活性剂之间的相互作用,通过芘准分子形成,透射电子显微镜和动态光散射探测","authors":"Ryan Lloyd, Abdullah Ba Salem, Noah Gallant and Jean Duhamel*, ","doi":"10.1021/acs.langmuir.4c0344910.1021/acs.langmuir.4c03449","DOIUrl":null,"url":null,"abstract":"<p >The interactions between calf thymus DNA and a pyrene-labeled gemini surfactant termed PyO-3–12 were investigated by using dynamic light scattering (DLS), transmission electron microscopy (TEM), and pyrene excimer formation (PEF) between an excited and a ground-state pyrene. PyO-3–12 was prepared with two dimethylammonium bromide headgroups linked with a propyl spacer, with one ammonium bearing a dodecyl tail and the other bearing a 1-pyrenemethoxyhexyl pendent. The size and electrostatic properties of the colloidal species were characterized by DLS, and TEM was used to describe the overall dimensions and morphologies of the aggregates. PEF enabled the study of PyO-3–12 at the molecular level. The association of PyO-3–12 and DNA was studied in detail for two specific PyO-3–12 concentrations of 16 and 56 μM using a (∓) ratio equal to the [DNA]/[PyO-3–12] ratio with [DNA] expressed in terms of DNA base pairs, yielding a (∓) ratio ranging from 0.1 to 10. An increase in PyO-3–12 association upon adding DNA was detected through an increase in PEF. Analysis of the fluorescence decays indicated a progressive binding of PyO-3–12 to DNA until the equicharge point was reached after which all PyO-3–12 surfactants were bound to DNA. The formation of large colloidal aggregates was observed by DLS, which showed a spike in the hydrodynamic diameter (<i>D</i><sub>h</sub>) as the (∓) ratio approached unity. Analysis of the fluorescence spectra suggested that the excited pyrenyl labels experienced a more hydrophobic environment for the lipoplexes generated by the 56 μM PyO-3–12 solutions, which appeared smaller and more globular in the TEM images than the lipoplexes obtained with the lower 16 μM PyO-3–12 concentration. Together, these experiments suggest that the concentrations of the cationic gemini surfactants and DNA are important parameters for the morphology of lipoplexes with possible implications for their transfection efficiency.</p>","PeriodicalId":50,"journal":{"name":"Langmuir","volume":"41 6","pages":"3768–3778 3768–3778"},"PeriodicalIF":3.9000,"publicationDate":"2025-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Interactions between DNA and a Pyrene-Labeled Surfactant Probed by Pyrene Excimer Formation, Transmission Electron Microscopy, and Dynamic Light Scattering\",\"authors\":\"Ryan Lloyd, Abdullah Ba Salem, Noah Gallant and Jean Duhamel*, \",\"doi\":\"10.1021/acs.langmuir.4c0344910.1021/acs.langmuir.4c03449\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The interactions between calf thymus DNA and a pyrene-labeled gemini surfactant termed PyO-3–12 were investigated by using dynamic light scattering (DLS), transmission electron microscopy (TEM), and pyrene excimer formation (PEF) between an excited and a ground-state pyrene. PyO-3–12 was prepared with two dimethylammonium bromide headgroups linked with a propyl spacer, with one ammonium bearing a dodecyl tail and the other bearing a 1-pyrenemethoxyhexyl pendent. The size and electrostatic properties of the colloidal species were characterized by DLS, and TEM was used to describe the overall dimensions and morphologies of the aggregates. PEF enabled the study of PyO-3–12 at the molecular level. The association of PyO-3–12 and DNA was studied in detail for two specific PyO-3–12 concentrations of 16 and 56 μM using a (∓) ratio equal to the [DNA]/[PyO-3–12] ratio with [DNA] expressed in terms of DNA base pairs, yielding a (∓) ratio ranging from 0.1 to 10. An increase in PyO-3–12 association upon adding DNA was detected through an increase in PEF. Analysis of the fluorescence decays indicated a progressive binding of PyO-3–12 to DNA until the equicharge point was reached after which all PyO-3–12 surfactants were bound to DNA. The formation of large colloidal aggregates was observed by DLS, which showed a spike in the hydrodynamic diameter (<i>D</i><sub>h</sub>) as the (∓) ratio approached unity. Analysis of the fluorescence spectra suggested that the excited pyrenyl labels experienced a more hydrophobic environment for the lipoplexes generated by the 56 μM PyO-3–12 solutions, which appeared smaller and more globular in the TEM images than the lipoplexes obtained with the lower 16 μM PyO-3–12 concentration. 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Interactions between DNA and a Pyrene-Labeled Surfactant Probed by Pyrene Excimer Formation, Transmission Electron Microscopy, and Dynamic Light Scattering
The interactions between calf thymus DNA and a pyrene-labeled gemini surfactant termed PyO-3–12 were investigated by using dynamic light scattering (DLS), transmission electron microscopy (TEM), and pyrene excimer formation (PEF) between an excited and a ground-state pyrene. PyO-3–12 was prepared with two dimethylammonium bromide headgroups linked with a propyl spacer, with one ammonium bearing a dodecyl tail and the other bearing a 1-pyrenemethoxyhexyl pendent. The size and electrostatic properties of the colloidal species were characterized by DLS, and TEM was used to describe the overall dimensions and morphologies of the aggregates. PEF enabled the study of PyO-3–12 at the molecular level. The association of PyO-3–12 and DNA was studied in detail for two specific PyO-3–12 concentrations of 16 and 56 μM using a (∓) ratio equal to the [DNA]/[PyO-3–12] ratio with [DNA] expressed in terms of DNA base pairs, yielding a (∓) ratio ranging from 0.1 to 10. An increase in PyO-3–12 association upon adding DNA was detected through an increase in PEF. Analysis of the fluorescence decays indicated a progressive binding of PyO-3–12 to DNA until the equicharge point was reached after which all PyO-3–12 surfactants were bound to DNA. The formation of large colloidal aggregates was observed by DLS, which showed a spike in the hydrodynamic diameter (Dh) as the (∓) ratio approached unity. Analysis of the fluorescence spectra suggested that the excited pyrenyl labels experienced a more hydrophobic environment for the lipoplexes generated by the 56 μM PyO-3–12 solutions, which appeared smaller and more globular in the TEM images than the lipoplexes obtained with the lower 16 μM PyO-3–12 concentration. Together, these experiments suggest that the concentrations of the cationic gemini surfactants and DNA are important parameters for the morphology of lipoplexes with possible implications for their transfection efficiency.
期刊介绍:
Langmuir is an interdisciplinary journal publishing articles in the following subject categories:
Colloids: surfactants and self-assembly, dispersions, emulsions, foams
Interfaces: adsorption, reactions, films, forces
Biological Interfaces: biocolloids, biomolecular and biomimetic materials
Materials: nano- and mesostructured materials, polymers, gels, liquid crystals
Electrochemistry: interfacial charge transfer, charge transport, electrocatalysis, electrokinetic phenomena, bioelectrochemistry
Devices and Applications: sensors, fluidics, patterning, catalysis, photonic crystals
However, when high-impact, original work is submitted that does not fit within the above categories, decisions to accept or decline such papers will be based on one criteria: What Would Irving Do?
Langmuir ranks #2 in citations out of 136 journals in the category of Physical Chemistry with 113,157 total citations. The journal received an Impact Factor of 4.384*.
This journal is also indexed in the categories of Materials Science (ranked #1) and Multidisciplinary Chemistry (ranked #5).