• Interaction

    AccNo. 21953 Score 0.86
    Name CRSTR_heart_ec Environment in vivo
    Kd 1.0 Organism Mus musculus (Mouse)

    Peptide

    AccNo. 21837
    Name CRSTR
    Organism N/A
    Constraint disulfide
    Sequence CRSTRANPC
    21837_small
    Origin phage display
    Form phage
    Internalized no
    Unnatural no
    Imaging no
    Is Motif no

    Interactor

    AccNo. 21685
    Name heart_ec
    Description heart vascular endothelial cells
    Organism Mus musculus (Mouse)
    Type tissue

    Experiment

    AccNo. 21889
    Classification incorrect?
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    Voting_motivation
    CA CVD DM APO ANG MI BD
    1.00 1.00 1.00 0.59 0.68 1.00 0.60 Vote
    plus plus plus plus plus plus plus Yes
    minus minus minus minus minus minus minus No
    Name PD_12
    Detection fluorescence microscopy, MI:0416
    Source PDF Text Id 12
    Journal Circulation. 2005 Sep 13;112(11):1601-11. Epub 2005 Sep 06.
    Title Molecular profiling of heart endothelial cells.
    Authors Zhang L, Hoffman JA, Ruoslahti E
    Text BACKGROUND: Endothelial cells that line the vascular lumen can express cell-surface proteins that are specific to the endothelium of a particular tissue. In this study, we probed the heart vasculature for heart-specific endothelial markers by phage display. METHODS AND RESULTS: We used a novel combination of in vivo phage selection and a bacterial 2-hybridization scheme against a heart cDNA library, which allows simultaneous identification of peptides that specifically bind to the target endothelium, as well as the endothelial molecules (receptors) recognized by the peptides. We found 5 heart-targeting peptides and their receptors. We confirmed and quantified the selective expression of 4 of the proteins in heart endothelial cells by independent methods. The heart specificity of phages was as high as 300-fold greater than that of nonrecombinant control phages. The proteins selectively expressed by the heart endothelium were in most cases also expressed by cardiomyocytes and, at lower levels, in some other tissues. CONCLUSIONS: These findings provide new markers for the endothelium of heart vessels and reveal a commonality between parenchymal and endothelial gene expression in the heart. The heart-homing peptides provide a means of targeting diagnostic and therapeutic agents to the heart, and their receptors are potential drug discovery targets.
    Mesh Terms Animals; Bacteriophages; Biological Markers/metabolism; Carrier Proteins/metabolism; Cells, Cultured; Coronary Vessels/cytology; Coronary Vessels/metabolism; Endothelial Cells/metabolism; Female; Injections, Intravenous; Ligands; Male; Mice; Mice, Inbred Strains; Myocardium/metabolism; Oligopeptides/administration & dosage; Oligopeptides/pharmacokinetics; Peptide Library; Peptides/metabolism; RNA, Messenger/metabolism; Receptors, Cell Surface/genetics; Receptors, Cell Surface/metabolism; Tissue Distribution; Two-Hybrid System Techniques
    References
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