Role of the gp85Trans-Sialidases in Trypanosoma cruzi Tissue Tropism Preferential Binding of a Conserved Peptide Motif to the Vasculature In Vivo 英文参考文献.docVIP
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Role of the gp85Trans-Sialidases in Trypanosoma cruzi Tissue Tropism Preferential Binding of a Conserved Peptide Motif to the Vasculature In Vivo 英文参考文献
Roleofthegp85/Trans-SialidasesinTrypanosomacruzi
TissueTropism:PreferentialBindingofaConserved
PeptideMotiftotheVasculatureInVivo
RenataR.Tonelli1,RicardoJ.Giordano2,ElenaMagdaBarbu3,AnaClaudiaTorrecilhas2,GersonS.
Kobayashi2,RobertR.Langley4,WadihArap3,RenataPasqualini3,WalterColli2,MariaJu′liaM.Alves2*
1DepartamentodeMicrobiologia,ImunologiaeParasitologia,UniversidadeFederaldeSa?oPaulo,Sa?oPaulo,Brazil,2DepartamentodeBioqu?′mica,InstitutodeQu?′mica,
UniversidadedeSa?o Paulo,Sa?o Paulo,Brazil,3DavidH.KochCenter,TheUniversityofTexasMDAndersonCancerCenter,Houston,Texas,UnitedStatesofAmerica,
4DepartmentofCancerBiology,TheUniversityofTexasMDAndersonCancerCenter,Houston,Texas,UnitedStatesofAmerica
Abstract
Background: Transmitted by blood-sucking insects, the unicellular parasite Trypanosoma cruzi is the causative agent of
Chagas’ disease, a malady manifested in a variety of symptoms from heart disease to digestive and urinary tract
dysfunctions.Thereasonsforsuchorganpreferencehavebeenamatterofgreatinterestinthefield,particularlybecause
the parasite can invade nearly every cell line and it can be found in most tissues following an infection. Among the
molecularfactorsthatcontributetovirulenceisalargemultigenefamilyofproteinsknownasgp85/trans-sialidase,which
participatesincellattachmentandinvasion.Butwhethertheseproteinsalsocontributetotissuehominghadnotyetbeen
investigated. Here, a combination of endothelial cell immortalization and phage display techniques has been used to
investigatetheroleofgp85/trans-sialidaseinbindingtothevasculature.
Methods: Bacteriophage expressing an important peptide motif (denominated FLY) common to all gp85/trans-sialidase
proteinswasusedasasurrogatetoinvestigatetheinteractionofthismotifwiththeendotheliumcompartment.Forthat
purpose phage particles were incubated with endothelial cells obtained from different organs or injected into mice
intravenously and the number of phage particles bound to cells or tissues was determined. Binding of p
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