Intrinsic curvature induced packing heterogeneity and non-uniform distribution of cholesterol and Abeta peptide in lipid bilayers
固有曲率诱导脂质双层中胆固醇和 Abeta 肽的堆积异质性和不均匀分布
基本信息
- 批准号:10333107
- 负责人:
- 金额:$ 10.88万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2022
- 资助国家:美国
- 起止时间:2022-07-01 至 2026-06-30
- 项目状态:未结题
- 来源:
- 关键词:Amyloid beta-ProteinAreaBehaviorBiologicalBrainCharacteristicsChargeCholesterolDetectionDevelopmentElectron Spin Resonance SpectroscopyElectrostaticsEvolutionExhibitsFluorescenceGelGlycerolGoalsGrowthHeterogeneityHydrophobicityIndividualKnowledgeLengthLipid BilayersLipidsLiquid substanceMeasuresMembraneMembrane FluidityMethodologyMethodsMicroscopyMovementPeptidesPharmaceutical PreparationsPhasePhosphorylcholinePositioning AttributePropertyReportingResearchResolutionShapesStressStructureVariantVesicleexperimental studyfluorophoreimprovedinnovationlaurdanmeltingneurotoxicneurotoxicitynovelpreferenceredshiftsecond harmonic
项目摘要
Project Summary: Lipid intrinsic curvature is a fundamental physical feature that regulates membrane
interactions. The goal is to elucidate intrinsic curvature induced effects on the growth of membrane curvature
and packing heterogeneity upon mixing lipids of dissimilar curvature and the consequent distribution of
cholesterol and the neurotoxic 25-35 segment of Aβ peptides in bilayers, using a novel steady state fluorescence
method that utilizes the computed second harmonic (SH) of the zeroth order spectra to better resolve spectral
lines that are not obvious in the zeroth harmonic. The polarity sensitive fluorophore Laurdan will be employed.
Laurdan emission in bilayers is a composite of a line, referred to as blue, from the denser packed region at 432
nm and a red line from the less packed region starting at 440 nm in single component gel phases evolving to
490 nm upon melting or mixing with a higher curvature lipid. This path of structure evolution was a new finding.
The present hypothesis is: Any added molecule of a dissimilar curvature enters the less packed region of the
bilayer. A higher curvature molecule increases stress which is then relieved by growth in flat domains. Laurdan’s
preference for flat regions together with growth in such domains contribute to an increase in Laurdan presence
in flat domains. Fluorescence spectra register an increase in the area, Ab, of the blue line from flat domains and
decrease in the red line area, Ar, along with a red-shift of the red peak and no shift in the blue peak. A lower
curvature molecule decreases stress and the membrane tends toward a homogeneous curvature distribution
resulting in an Ab decrease, Ar increase, blue shift of the red peak and no shift of the blue peak. Enhancement
of heterogeneity in regional curvature due to dissimilarity of intrinsic curvature of mixing lipids and preferential
distribution of cholesterol or Aβ peptide that manifest distinct difference in behaviors of areas and peak positions
are predicted. Laurdan fluorescence spectra will be measured without and with cholesterol or Aβ (25-35) in
mixed bilayers of (i and ii) 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) with (i) 1-palmitoyl-2-oleoyl-sn-
glycero-3-phosphocholine (POPC), and (ii) 1-palmitoyl-2-oleoyl-sn-glycero-3-phospho-(1′-rac-glycerol (POPG)
and (iii) brain lipids. SH of spectra will be computed to determine the number of elementary emissions. Spectra
will be fitted to this number of log-normal functions according to developed methodology to resolve spectral lines.
Area and peak position changes with mixture composition will be examined to determine packing heterogeneity
in the bilayers without the transmembrane molecules and the type of distribution (uniform or non-uniform) of
these molecules. Computing the SH of fluorescence spectra by modulating the wavenumber in analogy to field
modulation in ESR spectroscopy is an innovative approach to bring superior definition to features missed in
broad featureless in measured zeroth harmonics. The proposed research will significantly enhance current
knowledge by elucidating the key role of intrinsic curvature in the mechanism by which the added molecule
enters, accumulates preferentially, inhomogenously rigidifies the bilayer and changes its shape.
项目概述:脂质固有曲率是调节膜的基本物理特性
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Radha Ranganathan其他文献
Radha Ranganathan的其他文献
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{{ truncateString('Radha Ranganathan', 18)}}的其他基金
Intrinsic curvature induced packing heterogeneity and non-uniform distribution of cholesterol and Abeta peptide in lipid bilayers
固有曲率诱导脂质双层中胆固醇和 Abeta 肽的堆积异质性和不均匀分布
- 批准号:
10656172 - 财政年份:2022
- 资助金额:
$ 10.88万 - 项目类别:
Membrane Deformation and Mechanism of Stimulation of Phospholipase A2 by Oxidized Lipids
氧化脂质刺激磷脂酶A2的膜变形及机制
- 批准号:
9916778 - 财政年份:2018
- 资助金额:
$ 10.88万 - 项目类别:
Interface Quality Effects in Phospholipase Membrane Enzymology
磷脂酶膜酶学中的界面质量效应
- 批准号:
8265613 - 财政年份:2011
- 资助金额:
$ 10.88万 - 项目类别:
Interface Quality Effects in Phospholipase Membrane Enzymology
磷脂酶膜酶学中的界面质量效应
- 批准号:
8461141 - 财政年份:2011
- 资助金额:
$ 10.88万 - 项目类别:
Interface Quality Effects in Phospholipase Membrane Enzymology
磷脂酶膜酶学中的界面质量效应
- 批准号:
8076584 - 财政年份:2011
- 资助金额:
$ 10.88万 - 项目类别:
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