Evidence map›Paper›PMID 34576248›Full record

ReviewInternational journal of molecular sciences2021

Lipid Self-Assemblies under the Atomic Force Microscope.

Aritz B García-Arribas, Félix M Goñi, Alicia Alonso

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 40% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Surface Symphony: Orchestrating DPPC/DOPC Monolayer Behavior.Microscopy research and technique · 2026
    Article
  2. Review
  3. Review
  4. Article
  5. Erythrocyte Membrane Nanomechanical Rigidity Is Decreased in Obese Patients.International journal of molecular sciences · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Aritz B García-ArribasInstituto Biofisika (CSIC, UPV/EHU), Universidad del País Vasco, 48940 Leioa, Spain.ORCID 0000-0003-1866-6647
Félix M GoñiInstituto Biofisika (CSIC, UPV/EHU), Universidad del País Vasco, 48940 Leioa, Spain.
Alicia AlonsoInstituto Biofisika (CSIC, UPV/EHU), Universidad del País Vasco, 48940 Leioa, Spain.ORCID 0000-0002-2730-7470
University of the Basque Country · ES

Funding

Eusko Jaurlaritza IT1264-19Ministerio de Economía, Industria y Competitividad, Gobierno de España PGC2018-099857-B-I00
6 · The paper itself

Abstract

Lipid model membranes are important tools in the study of biophysical processes such as lipid self-assembly and lipid-lipid interactions in cell membranes. The use of model systems to adequate and modulate complexity helps in the understanding of many events that occur in cellular membranes, that exhibit a wide variety of components, including lipids of different subfamilies (e.g., phospholipids, sphingolipids, sterols…), in addition to proteins and sugars. The capacity of lipids to segregate by themselves into different phases at the nanoscale (nanodomains) is an intriguing feature that is yet to be fully characterized in vivo due to the proposed transient nature of these domains in living systems. Model lipid membranes, instead, have the advantage of (usually) greater phase stability, together with the possibility of fully controlling the system lipid composition. Atomic force microscopy (AFM) is a powerful tool to detect the presence of meso- and nanodomains in a lipid membrane. It also allows the direct quantification of nanomechanical resistance in each phase present. In this review, we explore the main kinds of lipid assemblies used as model membranes and describe AFM experiments on model membranes. In addition, we discuss how these assemblies have extended our knowledge of membrane biophysics over the last two decades, particularly in issues related to the variability of different model membranes and the impact of supports/cytoskeleton on lipid behavior, such as segregated domain size or bilayer leaflet uncoupling.

Indexed as

BiophysicsCell MembraneCytoskeletonLipid BilayersLipidsMembrane LipidsMembrane MicrodomainsMicroscopy, Atomic ForcePhospholipidsSphingolipidsLipid BilayersLipidsMembrane LipidsPhospholipidsSphingolipidsatomic force microscopycell membraneslipid assembliesmodel membranesnanodomainsphospholipidssphingolipidssupported planar bilayers

Identifiers

PMID34576248
PMCPMC8467407
OpenAlexW3199224416

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.