RECORD
Contribution of dipolar bridging to phospholipid membrane interactions: a mean-field analysis
Soft Condensed Matter · Submitted 10 Apr 2021
abstract compiled · 2026-09-23 · no language-model review
The authors' main claim In the mean-field regime of monovalent salt, the electrostatic forces between the membranes are characterized by a non-uniform trend: at large membrane separations, the interfacial dipoles on the opposing sides behave as like-charge cations and give rise to repulsive membrane interactions; at short membrane separations, the anionic field induced by the dipolar phosphate groups sets the behavior in the intermembrane region.
The compiled record
The paper's own sentences, arranged. Each label is drawn from a closed vocabulary; the number beside it is the probability the classifier gave that label. Numbers in the tables are the authors', checked by code. No sentence in this record was written by a model.
Open the compiled record
The abstract, sentence by sentence
We develop a model of interacting zwitterionic membranes with rotating surface dipoles immersed in a monovalent salt, and implement it in a field theoretic formalism. In the mean-field regime of monovalent salt, the electrostatic forces between the membranes are characterized by a non-uniform trend: at large membrane separations, the interfacial dipoles on the opposing sides behave as like-charge cations and give rise to repulsive membrane interactions; at short membrane separations, the anionic field induced by the dipolar phosphate groups sets the behavior in the intermembrane region. The attraction of the cationic nitrogens in the dipolar lipid headgroups leads to the adhesion of the membrane surfaces via dipolar bridging. The underlying competition between the opposing field components of the individual dipolar charges leads to the non-uniform salt ion affinity of the zwitterionic membrane with respect to the separation distance; large inter-membrane separations imply anionic excess while small, nanometer size separations, favor cationic excess. This complex ionic selectivity of zwitterionic membranes may have relevant repercussions on nanofiltration and nanofluidic transport techniques.
background contribution method result interpretation main claim
| # | sentence | role | the authors' own work | states the main conclusion | strength |
|---|---|---|---|---|---|
| s0 | We develop a model of interacting zwitterionic membranes with rotating surface dipoles immersed in a monovalent salt, and implement it in a field theoretic formalism. | method 0.54 | 0.95 | 0.03 | asserted 0.97 |
| s1 | In the mean-field regime of monovalent salt, the electrostatic forces between the membranes are characterized by a non-uniform trend: at large membrane separations, the interfacial dipoles on the opposing sides behave as like-charge cations and give rise to repulsive membrane interactions; at short membrane separations, the anionic field induced by the dipolar phosphate groups sets the behavior in the intermembrane region. | result 1.00 | 0.85 | 0.36 | asserted 1.00 |
| s2 | The attraction of the cationic nitrogens in the dipolar lipid headgroups leads to the adhesion of the membrane surfaces via dipolar bridging. | result 0.91 | 0.81 | 0.37 | asserted 1.00 |
| s3 | The underlying competition between the opposing field components of the individual dipolar charges leads to the non-uniform salt ion affinity of the zwitterionic membrane with respect to the separation distance; large inter-membrane separations imply anionic excess while small, nanometer size separations, favor cationic excess. | result 0.89 | 0.83 | 0.19 | asserted 1.00 |
| s4 | This complex ionic selectivity of zwitterionic membranes may have relevant repercussions on nanofiltration and nanofluidic transport techniques. | interpretation 0.99 | 0.25 | 0.11 | hedged possibility 1.00 |
What was examined, and what was not
- arXiv listing abstract v2
- full text
- figures and tables
- references and citing sentences
- relations to other papers
- P abstract
- S sections
- T body sentences
- C citations
- R cross-paper relations
The paper
Original abstract
We develop a model of interacting zwitterionic membranes with rotating surface dipoles immersed in a monovalent salt, and implement it in a field theoretic formalism. In the mean-field regime of monovalent salt, the electrostatic forces between the membranes are characterized by a non-uniform trend: at large membrane separations, the interfacial dipoles on the opposing sides behave as like-charge cations and give rise to repulsive membrane interactions; at short membrane separations, the anionic field induced by the dipolar phosphate groups sets the behavior in the intermembrane region. The attraction of the cationic nitrogens in the dipolar lipid headgroups leads to the adhesion of the membrane surfaces via dipolar bridging. The underlying competition between the opposing field components of the individual dipolar charges leads to the non-uniform salt ion affinity of the zwitterionic membrane with respect to the separation distance; large inter-membrane separations imply anionic excess while small, nanometer size separations, favor cationic excess. This complex ionic selectivity of zwitterionic membranes may have relevant repercussions on nanofiltration and nanofluidic transport techniques.
Human review
Discussion
Know something about this paper? Leave a comment, or highlight any passage above to comment on it.