<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>4</volume><submitter>Conzelmann N</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>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.&lt;h4>Findings&lt;/h4>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.&lt;h4>Conclusions&lt;/h4>We conclude that larger coherent parts of the protein or dimerisin</pubmed_abstract><journal>BMC research notes</journal><pagination>194</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3132715</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A screen for peptide agonists of the G-CSF receptor.</pubmed_title><pmcid>PMC3132715</pmcid><pubmed_authors>Conzelmann N</pubmed_authors><pubmed_authors>Schneider A</pubmed_authors></additional><is_claimable>false</is_claimable><name>A screen for peptide agonists of the G-CSF receptor.</name><description>&lt;h4>Background&lt;/h4>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.&lt;h4>Findings&lt;/h4>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.&lt;h4>Conclusions&lt;/h4>We conclude that larger coherent parts of the protein or dimerisin</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Jun</publication><modification>2025-05-29T20:30:19.394Z</modification><creation>2019-03-27T03:06:54Z</creation></dates><accession>S-EPMC3132715</accession><cross_references><pubmed>21676239</pubmed><doi>10.1186/1756-0500-4-194</doi></cross_references></HashMap>