Evidence map›Paper›PMID 23701821›Full record

ArticleChemistry and physics of lipids

Lateral diffusion of peripheral membrane proteins on supported lipid bilayers is controlled by the additive frictional drags of (1) bound lipids and (2) protein domains penetrating into the bilayer hydrocarbon core.

Brian P Ziemba, Joseph J Falke

Open access · greenAbstract read
In one paragraph

Article in Chemistry and physics of lipids. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

41 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
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  4. Enzymatic Reactions Dictated by the 2D Membrane Environment.The journal of physical chemistry letters · 2025
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  6. Membrane localization accelerates association under conditions relevant to cellular signaling.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  8. Synaptophysin chaperones the assembly of 12 SNAREpins under each ready-release vesicle.Proceedings of the National Academy of Sciences of the United States of America · 2023
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  13. Cadherin cis and trans interactions are mutually cooperative.Proceedings of the National Academy of Sciences of the United States of America · 2021
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  14. Review
  15. Article
  16. Structured clustering of the glycosphingolipid GM1 is required for membrane curvature induced by cholera toxin.Proceedings of the National Academy of Sciences of the United States of America · 2020
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  17. Article
  18. Review
  19. Article
  20. Cholesterol promotes Cytolysin A activity by stabilizing the intermediates during pore formation.Proceedings of the National Academy of Sciences of the United States of America · 2018
    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

2 authors at 1 institution in 1 country.

Brian P ZiembaDepartment of Chemistry and Biochemistry and the Molecular Biophysics Program, University of Colorado, Boulder, CO 80309-0596, USA.
Joseph J Falke
University of Colorado Boulder · US

Funding

Mechanisms of Signaling on Membrane SurfacesR01GM063235 · NIGMS · UNIVERSITY OF COLORADO AT BOULDER · PI FALKE, JOSEPH J · 2001 to 2021
$6.4M
NIGMS NIH HHS R01 GM-063235NIGMS NIH HHS R01 GM063235
6 · The paper itself

Abstract

Peripheral membrane proteins bound to lipids on bilayer surfaces play central roles in a wide array of cellular processes, including many signaling pathways. These proteins diffuse in the plane of the bilayer and often undergo complex reactions involving the binding of regulatory and substrate lipids and proteins they encounter during their 2D diffusion. Some peripheral proteins, for example pleckstrin homology (PH) domains, dock to the bilayer in a relatively shallow position with little penetration into the bilayer. Other peripheral proteins exhibit more complex bilayer contacts, for example classical protein kinase C isoforms (PKCs) bind as many as six lipids in stepwise fashion, resulting in the penetration of three PKC domains (C1A, C1B, C2) into the bilayer headgroup and hydrocarbon regions. A molecular understanding of the molecular features that control the diffusion speeds of proteins bound to supported bilayers would enable key molecular information to be extracted from experimental diffusion constants, revealing protein-lipid and protein-bilayer interactions difficult to study by other methods. The present study investigates a range of 11 different peripheral protein constructs comprised by 1-3 distinct domains (PH, C1A, C1B, C2, anti-lipid antibody). By combining these constructs with various combinations of target lipids, the study measures 2D diffusion constants on supported bilayers for 17 different protein-lipid complexes. The resulting experimental diffusion constants, together with the known membrane interaction parameters of each complex, are used to analyze the molecular features correlated with diffusional slowing and bilayer friction. The findings show that both (1) individual bound lipids and (2) individual protein domains that penetrate into the hydrocarbon core make additive contributions to the friction against the bilayer, thereby defining the 2D diffusion constant. An empirical formula is developed that accurately estimates the diffusion constant and bilayer friction of a peripheral protein in terms of its number of bound lipids and its geometry of penetration into the bilayer hydrocarbon core, yielding an excellent global best fit (R(2) of 0.97) to the experimental diffusion constants. Finally, the observed additivity of the frictional contributions suggests that further development of current theory describing bilayer dynamics may be needed. The present findings provide constraints that will be useful in such theory development.

Indexed as

DiffusionHumansLipid BilayersMembrane ProteinsPhospholipases A2, CytosolicProtein BindingProtein IsoformsProtein Kinase CReceptors, Cytoplasmic and NuclearRecombinant ProteinsLipid BilayersMembrane Proteinsphosphatidylinositol receptorsPhospholipases A2, CytosolicProtein IsoformsProtein Kinase CReceptors, Cytoplasmic and NuclearRecombinant Proteins1,2-dioleoyl-sn-glycero-3-phosphoethanolamine-N-(biotinyl)1,2-dioleoyl-sn-glycero-3-phosphoethanolamine-N-[lissamine rhodamine B sulfonyl](3,4,5)P3 or PIP31,2-dioleoyl-sn-glycero-3-phosphoinositol-3,4,5-trisphosphate(4,5)P(2) or PIP(2)1,2-dioleoyl-sn-glycero-3-phosphoinositol-4,5-diphosphateAF555Alexa Fluor 555Biotinyl-PEC1A and C1BC1 domainC2C2 domaincPLA2cytosolic phospholipase A2DAGdiacylglycerol, 1,2-dioleoyl-sn-glyceroldithiothreitolDTTEDTAethylenediaminetetraacetic acidfirst conserved domains of classical protein kinase Cgeneral receptor for phosphoinositides isoform 1glutathione S-transferaseGRP1GSTLRB-PEPCPH domainphosphatidylcholine, 1,2-dioleoyl-sn-glycero-3-phosphocholinePhosphatidylinositol lipidphosphatidylserine, 1,2-dioleoyl-sn-glycero-3-phospho-l-serinephospho-pantethienyl-transferasePIPKCPKCαpleckstrin homology domainprotein kinase C isoform αPSsecond conserved domain of classical protein kinase CSfpsonicated unilamellar vesicleSUVTIRFMtotal internal reflection fluorescence microscopy

Identifiers

PMID23701821
PMCPMC3707953
OpenAlexW2030233204

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Registered trials

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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.