grant

Lipid functions in bacterial cell organization

Organization CARNEGIE INSTITUTION OF WASHINGTON, D.C.Location WASHINGTON, UNITED STATESPosted 21 Sept 2022Deadline 31 Jul 2027
NIHUS FederalResearch GrantFY2025AffectBacteriaBacterial InfectionsBiological FunctionBiological ProcessBradyrhizobiumCell BodyCell CycleCell Division CycleCell Membrane Lipid RaftsCell Membrane LipidsCell PolarityCell membraneCellsCellular MembraneCholesterolCytoplasmic MembraneEnvironmentEukaryotaEukaryoteHumanLifeLinkLipidsMediatingMembraneMembrane LipidsMembrane MicrodomainsMicrobeModern ManPlasma MembraneRegulationSphingolipid MicrodomainsSphingolipid-Cholesterol RaftsWorkbacteria infectionbacterial diseasebiophysical characteristicsbiophysical characterizationbiophysical measurementbiophysical parametersbiophysical propertiescellular polaritycholesterol analogendosymbiontflotillinflotillin-1lipid raftmembrane structuremicrobe pathogenmicrobial pathogenpathogenic microbeplasmalemma
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Full Description

Project Summary/Abstract: Cellular membranes can be organized by the formation of discrete
membrane microdomains (MMs), such as the cholesterol- and flotillin-rich “lipid rafts” found in

eukaryotes. In bacteria, little is understood about the spatial organization of the cell membrane.

Because this domain does not synthesize cholesterol or related eukaryotic lipids, it traditionally

has been assumed that they do not contain raft-like compartments. Hopanoid lipids are the

closest bacterial analogs of cholesterol, and my lab has found that they promote formation of

MMs in the facultative endosymbiont Bradyrhizobium diazoefficiens. These MMs have similar

biophysical properties as eukaryotic lipid rafts and are typically polarized, suggesting a link

between raft-like MMs and cell polarity. Here, I propose to assess whether hopanoid-mediated

MMs have similar compositions as eukaryotic lipid rafts and identify biological processes that

are coordinated in these regions (Project 1). We also will examine cell cycle and polarity

regulation in B. diazoefficiens, and whether it is affected by hopanoid-mediated MMs in both

free-living and host-associated environments (Project 2). These projects will help discover

fundamental paradigms of bacterial membrane organization that are likely to be shared with

human-associated microbes, and may uncover new parallels between bacterial and eukaryotic

subcellular organization.

Grant Number: 5R35GM147015-04
NIH Institute/Center: NIH

Principal Investigator: Brittany Belin

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