Evidence map›Paper›PMID 42143405›Full record

ArticleBiophysical journal2026

Quantifying interleaflet coupling of phase behavior and observing anti-registered phases in asymmetric lipid bilayers.

Kristen B Kennison-Cook, Averi M Cooper, Frederick A Heberle

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Article in Biophysical journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Kristen B Kennison-CookDepartment of Chemistry, University of Tennessee, Knoxville, TN 37996, USA.
Averi M CooperDepartment of Chemistry, University of Tennessee, Knoxville, TN 37996, USA.
Frederick A HeberleDepartment of Chemistry, University of Tennessee, Knoxville, TN 37996, USA; Department of Biochemistry and Biophysics, Stockholm University, Stockholm, Sweden; Science for Life Laboratory, Solna, Sweden. Electronic address: fheberle@utk.edu.

Funding

Coupling of lateral and transverse organization in complex biomembranesR01GM138887 · NIGMS · UNIVERSITY OF TENNESSEE KNOXVILLE · PI HEBERLE, FREDERICK A, WAXHAM, M. NEAL · 2020 to 2023
$1.7M
NIGMS NIH HHS R01 GM138887
6 · The paper itself

Abstract

Biological membranes are compositionally asymmetric, with distinct lipid mixtures in each leaflet, yet how this asymmetry influences lateral membrane organization remains poorly understood. Here, we use calcium-induced hemifusion to generate asymmetric giant unilamellar vesicles (aGUVs) and investigate how lipid composition modulates interleaflet coupling of liquid-liquid phase separation. Symmetric GUVs composed of cholesterol, the high-melting lipid DPPC, and a low-melting phosphatidylcholine (either 14:1-PC or 16:1-PC) were prepared at compositions exhibiting coexisting liquid-ordered (Lo) and liquid-disordered (Ld) phases. Hemifusion with a uniformly mixed supported lipid bilayer selectively altered the outer leaflet composition, producing aGUVs with controlled but variable asymmetry. Fluorescence measurements of outer leaflet exchange revealed substantial vesicle-to-vesicle variability, resulting in overlapping populations of phase-separated and uniformly mixed aGUVs. To account for this variability, we developed a statistical framework that jointly models the distribution of exchange fractions and the location of a phase boundary in asymmetric composition space, allowing all observed vesicles to contribute to the analysis. We find that aGUVs containing 14:1-PC require significantly greater outer leaflet exchange to abolish phase separation than those containing 16:1-PC. Only in the 14:1-PC system do we observe vesicles exhibiting coexistence of distinct anti-registered phases, a theoretically predicted but rarely observed regime consistent with large hydrophobic mismatch. By expressing symmetric and asymmetric miscibility boundaries in a common compositional framework, we introduce a phenomenological parameter, Δ

Indexed as

Lipid BilayersUnilamellar Liposomes1,2-DipalmitoylphosphatidylcholineCalciumCholesterolPhase SeparationPhase TransitionPhosphatidylcholines1,2-DipalmitoylphosphatidylcholineCalciumCholesterolLipid BilayersPhosphatidylcholinesUnilamellar Liposomesanti-registered bilayer phaseshemifusioninterleaflet couplingliquid-liquid phase separationmembrane asymmetry

Identifiers

PMID42143405
PMCPMC13288181

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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.