Literature DB >> 11171099

Anginex, a designed peptide that inhibits angiogenesis.

A W Griffioen1, D W van der Schaft, A F Barendsz-Janson, A Cox, H A Struijker Boudier, H F Hillen, K H Mayo.   

Abstract

Novel beta-sheet-forming peptide 33-mers, betapep peptides, have been designed by using a combination approach employing basic folding principles and incorporating short sequences from the beta-sheet domains of anti-angiogenic proteins. One of these designed peptides (betapep-25), named anginex, was observed to be potently anti-angiogenic. Anginex specifically inhibits vascular endothelial cell proliferation and induces apoptosis in these cells, as shown by flow-cytometric detection of sub-diploid cells, TUNEL (terminal deoxyribonucleotidyl transferase-mediated dUTP-nick-end labelling) analysis and cell morphology. Anginex also inhibits endothelial cell adhesion to and migration on different extracellular matrix components. Inhibition of angiogenesis in vitro is demonstrated in the sprout-formation assay and in vivo in the chick embryo chorio-allantoic membrane angiogenesis assay. Comparison of active and inactive betapep sequences allows structure-function relationships to be deduced. Five hydrophobic residues and two lysines appear to be crucial to activity. This is the first report of a designed peptide having a well-defined biological function as a novel cytokine, which may be an effective anti-angiogenic agent for therapeutic use against various pathological disorders, such as neoplasia, rheumatoid arthritis, diabetic retinopathy and restenosis.

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Year:  2001        PMID: 11171099      PMCID: PMC1221648          DOI: 10.1042/0264-6021:3540233

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  43 in total

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6.  IL-8 single-chain homodimers and heterodimers: interactions with chemokine receptors CXCR1, CXCR2, and DARC.

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5.  Beta-sheet is the bioactive conformation of the anti-angiogenic anginex peptide.

Authors:  Ruud P M Dings; Monica M Arroyo; Nathan A Lockwood; Loes I van Eijk; Judy R Haseman; Arjan W Griffioen; Kevin H Mayo
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