Cellular Internalization of a Cargo Complex with a Novel Peptide Derived from the Third Helix of the Islet-1 Homeodomain. Comparison with the Penetratin Peptide

Cellular translocation into a human Bowes melanoma cell line was investigated and compared for penetratin and pIsl, two peptides that correspond to the third helices of the related homeodomains, from the Antennapedia transcription factor of Drosophila and the rat insulin-1 gene enhancer protein, res...

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Published inBioconjugate chemistry Vol. 12; no. 6; pp. 911 - 916
Main Authors Kilk, Kalle, Magzoub, Mazin, Pooga, Margus, Eriksson, L. E. Göran, Langel, Ülo, Gräslund, Astrid
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 01.11.2001
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Summary:Cellular translocation into a human Bowes melanoma cell line was investigated and compared for penetratin and pIsl, two peptides that correspond to the third helices of the related homeodomains, from the Antennapedia transcription factor of Drosophila and the rat insulin-1 gene enhancer protein, respectively. Both biotinylated peptides internalized into the cells with similar efficacy, yielding an analogous intracellular distribution. When a large cargo protein, 63 kDa avidin, was coupled to either peptide, efficient cellular uptake for both the peptide−protein complexes was observed. The interactions between each peptide and SDS micelles were studied by fluorescence spectroscopy and acrylamide quenching of the intrinsic tryptophan (Trp) fluorescence. Both peptides interacted strongly and almost identically with the membrane mimicking environment. Compared to penetratin, the new transport peptide pIsl has only one Trp residue, which simplifies the interpretation of the fluorescence spectra and in addition has a native Cys residue, which may be used for alternative coupling reactions of cargoes of different character.
Bibliography:ark:/67375/TPS-SR34Q8Q2-X
istex:3071F1C8231BDF9B1441C82B40B8368231CB232D
ISSN:1043-1802
1520-4812
1520-4812
DOI:10.1021/bc0100298