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      Role of Interaction Range and Buoyancy on the Adhesion of Vesicles

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      Langmuir
      American Chemical Society

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          Abstract

          Vesicles on substrates play a fundamental role in many biological processes, ranging from neurotransmitter release at the synapse on small scales to the nutrient intake of trees by large vesicles. For these processes, the adsorption or desorption of vesicles to biological substrates is crucial. Consequently, it is important to understand the factors determining whether and for how long a vesicle adsorbs to a substrate and what shape it will adopt. Here, we systematically study the adsorption of a vesicle to planar substrates with short- and long-range interactions, with and without buoyancy. We assume an axially symmetric system throughout our simulations. Previous studies often considered a contact potential of zero range and neutral buoyancy. The interaction range alters the location and order of the adsorption transition and is particularly important for small vesicles, e.g., in the synapse. Whereas even small density differences between the inside and the outside of the vesicle give rise to strong buoyancy effects for large vesicles, e.g., giant unilamellar vesicles, as buoyancy effects scale with the fourth power of the vesicle size. We find that (i) an attractive membrane-substrate potential with nonzero spatial extension leads to a pinned state, where the vesicle benefits from the attractive membrane-substrate interaction without significant deformation. The adsorption transition is of first order and occurs when the substrate switches from repulsive to attractive. (ii) Buoyancy shifts the transversality condition, which relates the maximal curvature in the contact zone to the adhesion strength and bending rigidity, up/downward, depending on the direction of the buoyancy force. The magnitude of the shift is influenced by the range of the potential. For upward buoyancy, adsorbed vesicles are at most metastable. We determine the stability limit and the desorption mechanisms and compile the thermodynamic data into an adsorption diagram. Our findings reveal that buoyancy, as well as spatially extended interactions, are essential when quantitatively comparing experiments to theory.

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          Improved tangent estimate in the nudged elastic band method for finding minimum energy paths and saddle points

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            Wetting and spreading

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              Configurations of fluid membranes and vesicles

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                Author and article information

                Journal
                Langmuir
                Langmuir
                la
                langd5
                Langmuir
                American Chemical Society
                0743-7463
                1520-5827
                06 February 2024
                20 February 2024
                : 40
                : 7
                : 3376-3390
                Affiliations
                Institute for Theoretical Physics, Georg-August University , Friedrich-Hund-Platz 1, 37077 Göttingen, Germany
                Author notes
                Author information
                https://orcid.org/0009-0007-5768-289X
                https://orcid.org/0000-0002-7472-973X
                Article
                10.1021/acs.langmuir.3c02715
                10883059
                38319679
                44fac68c-d00d-4716-b971-104bc7956804
                © 2024 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 12 September 2023
                : 05 January 2024
                : 03 January 2024
                Funding
                Funded by: Deutsche Forschungsgemeinschaft, doi 10.13039/501100001659;
                Award ID: SPP 2171 - Mu 1674/17-1
                Funded by: Deutsche Forschungsgemeinschaft, doi 10.13039/501100001659;
                Award ID: SPP 2171 - Mu 1674/17-2
                Categories
                Article
                Custom metadata
                la3c02715
                la3c02715

                Physical chemistry
                Physical chemistry

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