2020
DOI: 10.1021/acs.langmuir.0c01810
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The Mechanism of Vesicle Solubilization by the Detergent Sodium Dodecyl Sulfate

Abstract: Membrane solubilization by sodium dodecyl sulfate (SDS) is indispensable for many established biotechnological applications, including viral inactivation and protein extraction. Although the ensemble thermodynamics have been thoroughly explored, the underlying molecular dynamics have remained inaccessible, owing to major limitations of traditional measurement tools. Here, we integrate multiple advanced biophysical approaches to gain multiangle insight into the time-dependence and fundamental kinetic steps asso… Show more

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Cited by 33 publications
(35 citation statements)
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“…The size distribution of the prepared vesicles in buffer solution is evaluated by dynamic light scattering using a Zetasizer µV molecular size detector (Malvern Instruments Ltd, UK), whereby a mean polydispersity index <0.3 is observed [25,27]. When the vesicles are doped with 0.1 molar% of the fluorescent membrane stain 1,1 ′dioctadecyl-3,3,3 ′ ,3 ′ -tetramethylindocarbocyanine perchlorate, wide-field total internal reflection fluorescence microscopy (λ ex = 532 nm, λ em = 570 nm) is used to quantify the number and concentration of surface-immobilised vesicles per 25 × 50 µm field of view [27]. Scanning electron microscope (SEM) micrographs confirm the vesicles have an expected size of about 100 ± 20 nm, presenting a spherical and intact shape without fusing on the surface (figure 2(b)), confirming the possibility to use them as excellent model for exosomes.…”
Section: Detection Of Biotinylated Vesiclesmentioning
confidence: 99%
“…The size distribution of the prepared vesicles in buffer solution is evaluated by dynamic light scattering using a Zetasizer µV molecular size detector (Malvern Instruments Ltd, UK), whereby a mean polydispersity index <0.3 is observed [25,27]. When the vesicles are doped with 0.1 molar% of the fluorescent membrane stain 1,1 ′dioctadecyl-3,3,3 ′ ,3 ′ -tetramethylindocarbocyanine perchlorate, wide-field total internal reflection fluorescence microscopy (λ ex = 532 nm, λ em = 570 nm) is used to quantify the number and concentration of surface-immobilised vesicles per 25 × 50 µm field of view [27]. Scanning electron microscope (SEM) micrographs confirm the vesicles have an expected size of about 100 ± 20 nm, presenting a spherical and intact shape without fusing on the surface (figure 2(b)), confirming the possibility to use them as excellent model for exosomes.…”
Section: Detection Of Biotinylated Vesiclesmentioning
confidence: 99%
“…Different studies have investigated the micelle-to-vesicle transition (MVT) process, by which mixed micelles transform into vesicles, and their effect on the reconstituted (or encapsulated) components onto liposomes, by describing the (molecular and supramolecular) out-of-equilibrium processes and providing quantitative information on the intermediate (unstable) aggregates, partition coefficients, etc. [ 72 , 73 , 74 , 75 , 76 , 77 ].…”
Section: Conventional Methods For the Preparation Of Liposomesmentioning
confidence: 99%
“…Preparation of vesicles incorporating the DiI and DiD FRET sensor. Large unilamellar vesicles composed of 0.1 mol % DiI, 0.1 mol % DiD, 1 % biotin-PE and 98.8 mol % POPC were prepared as previously described (23,24). Briefly, lipids, DiI and Did were mixed in chloroform before the solvent was evaporated.…”
Section: Methodsmentioning
confidence: 99%