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A screen for peptide agonists of the G-CSF receptor

BACKGROUND: Granulocyte-colony stimulating factor (G-CSF) is one of the most important pharmacologically used proteins. Potential uses beyond the stimulation of neutrophilic granulocytes are the treatment of CNS disorders. Disadvantages of the G-CSF protein as a drug are its moderate plasma half-lif...

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Autores principales: Conzelmann, Nadine, Schneider, Armin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3132715/
https://www.ncbi.nlm.nih.gov/pubmed/21676239
http://dx.doi.org/10.1186/1756-0500-4-194
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author Conzelmann, Nadine
Schneider, Armin
author_facet Conzelmann, Nadine
Schneider, Armin
author_sort Conzelmann, Nadine
collection PubMed
description BACKGROUND: Granulocyte-colony stimulating factor (G-CSF) is one of the most important pharmacologically used proteins. Potential uses beyond the stimulation of neutrophilic granulocytes are the treatment of CNS disorders. Disadvantages of the G-CSF protein as a drug are its moderate plasma half-life time and considerable production costs. We therefore conducted a screen for peptide agonists derived from the sequence of human G-CSF. FINDINGS: Despite of the high sensitivity of our screening system we could not detect any positive hits in a single peptide approach. In a multiplex approach using a permutation of any combination of 10 different peptides we could also not detect a positive block. CONCLUSIONS: We conclude that larger coherent parts of the protein or dimerising peptides may be needed to achieve activation of the receptor.
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spelling pubmed-31327152011-07-12 A screen for peptide agonists of the G-CSF receptor Conzelmann, Nadine Schneider, Armin BMC Res Notes Project Note BACKGROUND: Granulocyte-colony stimulating factor (G-CSF) is one of the most important pharmacologically used proteins. Potential uses beyond the stimulation of neutrophilic granulocytes are the treatment of CNS disorders. Disadvantages of the G-CSF protein as a drug are its moderate plasma half-life time and considerable production costs. We therefore conducted a screen for peptide agonists derived from the sequence of human G-CSF. FINDINGS: Despite of the high sensitivity of our screening system we could not detect any positive hits in a single peptide approach. In a multiplex approach using a permutation of any combination of 10 different peptides we could also not detect a positive block. CONCLUSIONS: We conclude that larger coherent parts of the protein or dimerising peptides may be needed to achieve activation of the receptor. BioMed Central 2011-06-15 /pmc/articles/PMC3132715/ /pubmed/21676239 http://dx.doi.org/10.1186/1756-0500-4-194 Text en Copyright ©2011 Schneider et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Project Note
Conzelmann, Nadine
Schneider, Armin
A screen for peptide agonists of the G-CSF receptor
title A screen for peptide agonists of the G-CSF receptor
title_full A screen for peptide agonists of the G-CSF receptor
title_fullStr A screen for peptide agonists of the G-CSF receptor
title_full_unstemmed A screen for peptide agonists of the G-CSF receptor
title_short A screen for peptide agonists of the G-CSF receptor
title_sort screen for peptide agonists of the g-csf receptor
topic Project Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3132715/
https://www.ncbi.nlm.nih.gov/pubmed/21676239
http://dx.doi.org/10.1186/1756-0500-4-194
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