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Modulation of muscle contraction by a cell-permeable peptide.

Tünnemann, Gisela ; Karczewski, Peter ; Haase, Hannelore ; Cardoso, M. Cristina ; Morano, Ingo (2007)
Modulation of muscle contraction by a cell-permeable peptide.
In: Journal of molecular medicine, 85 (12)
Artikel, Bibliographie

Kurzbeschreibung (Abstract)

In contrast to immortal cell lines, primary cells are hardly susceptible to intracellular delivery methods such as transfection. In this study, we evaluated the direct delivery of several cell-permeable peptides under noninvasive conditions into living primary adult rat cardiomyocytes. We specifically monitored the functional effects of a cell-permeable peptide containing the 15 amino acid N-terminal peptide from human ventricular light chain-1 (VLC-1) on contraction and intracellular Ca2+ signals after electrical stimulation in primary adult cardiomyocytes. The transducible VLC-1 variant was taken up by cardiomyocytes within 5 min with more than 95% efficiency and localized to sarcomeric structures. Analysis of the functional effects of the cell-permeable VLC-1 revealed an enhancement of the intrinsic contractility of cardiomyocytes without affecting the intracellular Ca2+. Therefore, peptide transduction mediated by cell-penetrating peptides represents not only a unique strategy to enhance heart muscle function with no secondary effect on intracellular Ca2+ but also an invaluable tool for the modulation and manipulation of protein interactions in general and in primary cells.

Typ des Eintrags: Artikel
Erschienen: 2007
Autor(en): Tünnemann, Gisela ; Karczewski, Peter ; Haase, Hannelore ; Cardoso, M. Cristina ; Morano, Ingo
Art des Eintrags: Bibliographie
Titel: Modulation of muscle contraction by a cell-permeable peptide.
Sprache: Englisch
Publikationsjahr: 2007
Titel der Zeitschrift, Zeitung oder Schriftenreihe: Journal of molecular medicine
Jahrgang/Volume einer Zeitschrift: 85
(Heft-)Nummer: 12
URL / URN: http://www.cardoso-lab.org/publications/Tunnemann%202007-EPu...
Kurzbeschreibung (Abstract):

In contrast to immortal cell lines, primary cells are hardly susceptible to intracellular delivery methods such as transfection. In this study, we evaluated the direct delivery of several cell-permeable peptides under noninvasive conditions into living primary adult rat cardiomyocytes. We specifically monitored the functional effects of a cell-permeable peptide containing the 15 amino acid N-terminal peptide from human ventricular light chain-1 (VLC-1) on contraction and intracellular Ca2+ signals after electrical stimulation in primary adult cardiomyocytes. The transducible VLC-1 variant was taken up by cardiomyocytes within 5 min with more than 95% efficiency and localized to sarcomeric structures. Analysis of the functional effects of the cell-permeable VLC-1 revealed an enhancement of the intrinsic contractility of cardiomyocytes without affecting the intracellular Ca2+. Therefore, peptide transduction mediated by cell-penetrating peptides represents not only a unique strategy to enhance heart muscle function with no secondary effect on intracellular Ca2+ but also an invaluable tool for the modulation and manipulation of protein interactions in general and in primary cells.

Fachbereich(e)/-gebiet(e): 10 Fachbereich Biologie > Cell Biology and Epigenetics
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10 Fachbereich Biologie
Hinterlegungsdatum: 06 Mär 2010 15:45
Letzte Änderung: 05 Mär 2013 09:32
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