grant

Mapping the Interactions and Dynamics that Organize Bacteria Cells

Organization UNIVERSITY OF MICHIGAN AT ANN ARBORLocation ANN ARBOR, UNITED STATESPosted 1 Jun 2022Deadline 31 Mar 2027
NIHUS FederalResearch GrantFY2025AddressBacteriaBacterial ModelBacteriologyBiochemical ReactionBiochemistryBiological ChemistryBiologyBiophysicsBlue-Green AlgaeBlue-Green BacteriaC crescentusC. crescentusCaulobacter crescentusCell BodyCell FunctionCell PhysiologyCell ProcessCellsCellular FunctionCellular PhysiologyCellular ProcessCellular biologyColorCommunitiesCyanobacteriumCyanophyceaeCyanophytaDNAData SetDeoxyribonucleic AcidDetectionDiffusionDiseaseDisorderE coliE. coliEnzymatic ReactionEscherichia coliEukaryotaEukaryoteFluorescenceGoalsHealthHumanImageImaging DeviceImaging InstrumentImaging ToolIn VitroMapsMeasurementMeasuresMethodsModelingModern ManMolecularMotionOrganization ChartsOutcomePhasePhysical condensationPositionPositioning AttributeProkaryotaeProkaryotic CellsProteinsResolutionRibonucleoproteinsRoleStructureSubcellular ProcessSystemTestingTimeTubeWorkanalytical toolbiophysical foundationbiophysical principlesbiophysical sciencescell biologycell fixingcell typecommensal bacteriacommensal bacterial speciescondensationdata qualitydiffuseddiffusesdiffusingdiffusionsfightinghuman diseaseimagingimprovedin vitro Modelinnovateinnovationinnovativemicrobialmolecular scalenanonano meter scalenano meter sizednanometer scalenanometer sizednanoscalenew approachesnext generationnovelnovel approachesnovel strategiesnovel strategyorganizational structureprokaryoteresolutionsscaffoldscaffoldingsingle moleculesocial rolespatial and temporalspatial temporalspatiotemporalstatisticssuper high resolutionsuperresolutionsuperresolution imagingsuperresolution microscopytoolultra high resolution
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Full Description

Project Summary
Molecular-scale interactions enable subcellular organization, but the current state-of-the-art does not include a

generalizable method for measuring how molecules move and cooperate on the nanometer scale and in real

time within the cell. This gap is particularly striking in bacteria cells. Accordingly, our picture of the organization

of the bacterial cell is incomplete. This proposal aims to understand how cellular components organize—by

scaffolding, aggregation, phase separation, or otherwise—to produce a general model of bacterial cell

organization and ultimately enable us to promote commensal bacteria or fight human disease. Thus, we aim to

measure the positioning, interactions, and motions of molecules in living bacterial cells in different protein

systems implicated in the sub-cellular organization of these cells. This proposal will develop these next-

generation super-resolution tools through three synergistic specific aims: (1) to super-resolve how single-

molecule dynamics vary in space and in time in living bacterial cells; (2) to super-resolve sub-cellular interactions

in space and time in living bacteria cells; and (3) to improve the detection of single molecules in living bacteria

cells. The toolkit that we develop to map molecular motions and interactions will be broadly applicable to the

single-molecule bacteriology community. Furthermore, by focusing on applications in bacterial cell biology, the

tools developed in this project will have a widespread, positive biomedical impact by making accessible long-

term, significant questions in microbial biology.

Grant Number: 5R01GM144731-04
NIH Institute/Center: NIH

Principal Investigator: Julie Biteen

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