grant

Determining the cellular and nanoscale localization of Synaptotagmin VII

Organization THOMAS JEFFERSON UNIVERSITYLocation PHILADELPHIA, UNITED STATESPosted 5 Dec 2022Deadline 31 Jul 2026
NIHUS FederalResearch GrantFY2026ATRAAgreementApoptosisApoptosis PathwayApplications GrantsArchitectureAssayAwardAxon TerminalsBioassayBiochemicalBiochemistryBiological AssayBiological ChemistryBiotinylationBipolar Affective PsychosisBipolar DisorderBrainBrain CancerBrain Nervous SystemCNS Nervous SystemCalciumCancer GenesCancer-Promoting GeneCancersCell Surface ProteinsCell membraneCell surfaceCentral Nervous SystemColorCommon Rat StrainsCytoplasmic MembraneDLG4DLG4 geneDataDiseaseDisorderDockingDysfunctionEncephalonEngineering / ArchitectureFamily memberFellowshipFugu ToxinFunctional disorderGRIN1GluN1Grant ProposalsHead and Neck CancerHead and Neck CarcinomaImageLearningLinkMalignant Head and Neck NeoplasmMalignant NeoplasmsMalignant TumorMalignant Tumor of the BrainMalignant neoplasm of brainManic-Depressive PsychosisMembrane Protein GeneMembrane ProteinsMembrane-Associated ProteinsMental disordersMental health disordersMiceMice MammalsMurineMusN-methyl-D-aspartate receptor subunit NR1NMDA receptor A1NMDAR1NMDARA1 proteinNerve CellsNerve Impulse TransmissionNerve TransmissionNerve UnitNervous System DiseasesNervous System DisorderNeural CellNeural TransmissionNeuraxisNeurocyteNeurologic DisordersNeurological DisordersNeuronal TransmissionNeuronsOncogenesPSD95PhysiciansPhysiopathologyPlasma MembranePreparationPresynaptic Nerve EndingsPresynaptic TerminalsProgrammed Cell DeathProstateProstate GlandProstatic GlandProtein FamilyProteinsPsychiatric DiseasePsychiatric DisorderPublishingRatRats MammalsRattusRecyclingRetinoic AcidRoleSAP90ScientistSiteSliceSpinal ColumnSpineStaining methodStainsStructural ModelsStructureSurfaceSurface ProteinsSynapsesSynapticSynaptic BoutonsSynaptic CleftSynaptic TerminalsSynaptic TransmissionSytVII proteinTarichatoxinTestingTetradotoxinTetrodotoxinTrainingTrans Vitamin A AcidTransforming GenesTransmissionTretinoinTretinoinumVertebral columnVesicleVitamin A AcidWorkall-trans-Retinoic Acidall-trans-Vitamin A acidaxon signalingaxon-glial signalingaxonal signalingbackbonebipolar affective disorderbipolar diseasebipolar illnessbipolar mood disorderchannel blockersdesigndesigningexperimentexperimental researchexperimental studyexperimentsglia signalingglial signalingglutamate receptor, ionotropic, N-methyl D-aspartate 1head/neck cancerimaginginhibitorinsightmalignancymalignant head and neck tumormanic depressive disordermanic depressive illnessmental illnessnano meter scalenano meter sizednanocolumnnanometer scalenanometer sizednanoscaleneoplasm/cancernerve signalingneural signalingneurological diseaseneuronalneuronal signalingneurotransmissionneurotransmitter releaseoverexpressoverexpressionpathophysiologyplasmalemmapostsynapticpreparationspresynapticprotein functionpsychiatric illnesspsychological disorderpuffer fish toxinsensorskillssocial rolesuper high resolutionsuperresolutionsuperresolution microscopysynapsesynaptotagminsynaptotagmin 7synaptotagmin VIItrans-Retinoic Acidtransmission processultra high resolutionultra resolutionultrafine resolutionvesicle releasevesicular release
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Full Description

ABSTRACT
Synaptic dysfunction is linked to numerous devastating neurological and psychiatric disease.

Synaptic transmission is initiated by the calcium dependent release of neurotransmitters. The calcium

sensors responsible for triggering vesicle release are the Synaptotagmins (SYT), a 17 protein family. The

function of one SYT, SYT7, is less well understood but is thought to be of significant importance due to its

broad expression throughout the body and brain, connections to cancer and ALS, and enigmatic function in

the central nervous system. Unlike other Synaptotagmins, SYT7 is thought to be found on the plasma

membrane and its function remains controversial. The role of SYT7 is still under intense debate due to

several outstanding questions regarding its cellular and synaptic localization. Answering these key questions

is the focus of my grant proposal and will provide necessary insights into SYT7’s function.

This proposal aims to answer these questions by determining SYT7’s cellular and nanoscale

localization in cortical neurons using biochemistry and three-color STED super resolution microscopy. Aim

1 will determine whether SYT7 is found on the cell surface of cortical neurons using live-cell surface protein

biotinylation and live-cell surface staining in mouse cortical slices and rat primary cortical neurons. Aim 2

will determine how SYT7 is organized at synapses using three-color STED staining for endogenous synaptic

proteins. Aim 3 will determine whether neuronal activity regulates the cellular and nanoscale localization of

SYT7 using both surface protein biotinylation and live-cell surface staining with three-color STED.

This proposal is designed to provide me with intellectual and technical training throughout the

fellowship award. I will learn key biochemical assays, ex vivo slice preparations, and will hone my skills in

advanced STED super resolution microscopy. With support from this award, the training during this

fellowship will provide me with the skills necessary to become a successful physician scientist.

Grant Number: 5F30NS130973-04
NIH Institute/Center: NIH

Principal Investigator: Rachel Cain

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