grant

Lipidic drivers of organelle function and dysregulation

Organization UNIVERSITY OF CALIFORNIA, SAN DIEGOLocation LA JOLLA, UNITED STATESPosted 1 Aug 2021Deadline 31 Jul 2026
NIHUS FederalResearch GrantFY202521+ years oldAdultAdult HumanAdult-Onset Diabetes MellitusApplied GeneticsBlindnessBody TissuesCell BodyCell FunctionCell LineCell Membrane LipidsCell PhysiologyCell ProcessCell membraneCellLineCellsCellular FunctionCellular PhysiologyCellular ProcessChemicalsCytoplasmic MembraneDegenerative Neurologic DisordersDevelopmentDiffusionDiseaseDisorderElectron TransportEngineeringGeneticGenetic DiseasesGoalsHealthHumanImageInner mitochondrial membraneIntermediary MetabolismKetosis-Resistant Diabetes MellitusKnowledgeLaboratoriesLinkLipidsMammalian CellMaturity-Onset Diabetes MellitusMechanicsMembraneMembrane BiologyMembrane LipidsMetabolic DiseasesMetabolic DisorderMetabolic ProcessesMetabolismMitochondriaModelingModern ManMolecularNIDDMNervous System Degenerative DiseasesNeural Degenerative DiseasesNeural degenerative DisordersNeurodegenerative DiseasesNeurodegenerative DisordersNeurologic Degenerative ConditionsNon-Insulin Dependent DiabetesNon-Insulin-Dependent Diabetes MellitusNoninsulin Dependent DiabetesNoninsulin Dependent Diabetes MellitusOrganellesOuter pigmented layer of retinaPhosphatidesPhospholipidsPigment cell layer of retinaPigmented layer of retinaPlasma MembraneResearchRespirationRetinal Pigment EpitheliumRetinal pigment epithelial cellsRoleSlow-Onset Diabetes MellitusSphingolipidsStable Diabetes MellitusStrains Cell LinesStructureStructure of retinal pigment epitheliumSubcellular ProcessSystemT2 DMT2DT2DMTestingThesaurismosisTissuesType 2 Diabetes MellitusType 2 diabetesType II Diabetes MellitusType II diabetesUnsaturated FatsViscosityYeastsadult onset diabetesadulthoodbiophysical approachesbiophysical methodologybiophysical methodsbiophysical modelbiophysical techniquescell behaviorcellular behaviorcultured cell linedegenerative diseases of motor and sensory neuronsdegenerative neurological diseasesdevelopmentaldiffuseddiffusesdiffusingdiffusionselectron transfergenetic approachgenetic conditiongenetic disordergenetic strategyimagingimaging approachimaging based approachketosis resistant diabetesmaturity onset diabetesmechanicmechanicalmembrane modelmembrane structuremetabolism disordermitochondrialmitochondrial dysfunctionneurodegenerative illnessplasmalemmaprogramsrespiratoryrespiratory mechanismsaturated dietary fatsaturated dietary lipidsaturated fatsaturated lipidserine C-palmitoyltransferaseserine palmitoyltransferasesocial roletooltype 2 DMtype II DMtype two diabetesunsaturated dietary fatunsaturated dietary lipidunsaturated lipidvision lossvisual loss
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Full Description

PROJECT SUMMARY
Lipids represent a diverse class of biomolecules that are the building blocks of cell membranes. In recent years,

alterations in lipid composition have been identified as hallmarks of numerous diseases, ranging from type 2

diabetes to neurodegenerative disorders. However, understanding the functional roles of bulk membrane lipids

has long been a challenge, in part due to the difficulties of manipulating and imaging them in cells. Our laboratory

applies genetic and chemical tools to study lipid function and develop biophysical models for membrane-

associated cellular processes. The proposed research program will carry out this approach to identify how two

disease-associated lipid perturbations alter the behavior of cellular compartments. In the first thrust, we will use

effects of saturated phospholipids on membrane viscosity to uncover how structure and dynamics control

respiratory metabolism. Specifically, we will engineer inner mitochondrial membrane composition in both yeast

and mammalian cell lines and use this perturbation to dissect the contributions of diffusion and supramolecular

assembly to the electron transport chain. This effort will uncover the function of conserved features of mammalian

mitochondria, such as respiratory supercomplexes, and test how increases in saturated lipids caused by

metabolic disorders could directly contribute to mitochondrial dysfunction. In the second thrust, we will use a

genetic system to interrogate the function of 1-deoxysphinglipids, non-canonical products of serine-

palmitoyltransferase that have been associated with several genetic and metabolic disorders. We will focus on

how synthesis of 1-deoxysphinglipids dysregulates the endomembrane system in retinal pigment epithelium

cells, which have been linked to adult-onset blindness caused by 1-deoxysphinglipid accumulation. Development

of new imaging approaches will broaden the impact of this thrust to the emerging biomedical roles for these

enigmatic lipids. If executed, the research program will thus generate models for two sets of lipids molecules and

their cellular points of action in both healthy and diseased cells. Our long-term goal is to understand how changes

in lipid composition across organelles, cells, and tissues arise and function, and use this knowledge to uncover

the molecular mechanisms underlying membrane biology.

Grant Number: 5R35GM142960-05
NIH Institute/Center: NIH

Principal Investigator: Itay Budin

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