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Neubacher, Henrik
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Neubacher, Henrik
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Neubacher, Henrik
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Neubacher, H.
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2014Journal Article Research Paper [["dc.bibliographiccitation.firstpage","4767"],["dc.bibliographiccitation.issue","16"],["dc.bibliographiccitation.journal","Langmuir"],["dc.bibliographiccitation.lastpage","4774"],["dc.bibliographiccitation.volume","30"],["dc.contributor.author","Neubacher, Henrik"],["dc.contributor.author","Mey, Ingo"],["dc.contributor.author","Carnarius, Christian"],["dc.contributor.author","Lazzara, Thomas D."],["dc.contributor.author","Steinem, Claudia"],["dc.date.accessioned","2017-09-07T11:46:17Z"],["dc.date.available","2017-09-07T11:46:17Z"],["dc.date.issued","2014"],["dc.description.abstract","Screening tools to study antimicrobial peptides (AMPs) with the aim to optimize therapeutic delivery vectors require automated and parallelized sampling based on chip technology. Here, we present the development of a chip-based assay that allows for the investigation of the action of AMPs on planar lipid membranes in a time-resolved manner by fluorescence readout. Anodic aluminum oxide (AAO) composed of cylindrical pores with a diameter of 70 nm and a thickness of up to 10 mu m was used as a support to generate pore-spanning lipid bilayers from giant unilamellar vesicle spreading, which resulted in large continuous membrane patches sealing the pores. Because AAO is optically transparent, fluid single lipid bilayers and the underlying pore cavities can be readily observed by three-dimensional confocal laser scanning microscopy (CLSM). To assay the permeabilizing activity of the AMPs, the translocation of the water-soluble dyes into the AAO cavities and the fluorescence of the sulforhodamine 101 1,2-dihexadecanoyl-sn-glycero-3-phosphoethanol-l-amine triethylammonium salt (Texas Red DHPE)-labeled lipid membrane were observed by CLSM in a time-resolved manner as a function of the AMP concentration. The effect of two different AMPs, magainin-2 and melittin, was investigated, showing that the concentrations required for membrane permeabilization and the kinetics of the dye entrance differ significantly. Our results are discussed in light of the proposed permeabilization models of the two AMPs. The presented data demonstrate the potential of this setup for the development of an on-chip screening platform for AMPs."],["dc.identifier.doi","10.1021/la500358h"],["dc.identifier.gro","3142140"],["dc.identifier.isi","000335297300029"],["dc.identifier.pmid","24707859"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/4988"],["dc.language.iso","en"],["dc.notes.intern","WoS Import 2017-03-10 / Funder: Deutsche Forschungsgemeinschaft (DFG) [SFB 803]"],["dc.notes.status","final"],["dc.notes.submitter","PUB_WoS_Import"],["dc.relation.issn","0743-7463"],["dc.title","Permeabilization Assay for Antimicrobial Peptides Based on Pore-Spanning Lipid Membranes on Nanoporous Alumina"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.subtype","original"],["dspace.entity.type","Publication"]]Details DOI PMID PMC WOS2013Conference Abstract [["dc.bibliographiccitation.journal","European Biophysics Journal"],["dc.bibliographiccitation.volume","42"],["dc.contributor.author","Neubacher, H."],["dc.contributor.author","Mey, Ingo"],["dc.contributor.author","Steinem, Claudia"],["dc.date.accessioned","2018-11-07T09:22:33Z"],["dc.date.available","2018-11-07T09:22:33Z"],["dc.date.issued","2013"],["dc.format.extent","S127"],["dc.identifier.isi","000330215300354"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/29372"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Springer"],["dc.publisher.place","New york"],["dc.relation.eventlocation","Lisbon, Portugal"],["dc.relation.issn","1432-1017"],["dc.relation.issn","0175-7571"],["dc.title","A model lipid bilayer system for the investigation on cell-penetrating peptides"],["dc.type","conference_abstract"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details WOS2011Conference Abstract [["dc.bibliographiccitation.firstpage","81"],["dc.bibliographiccitation.journal","European Biophysics Journal"],["dc.bibliographiccitation.lastpage","82"],["dc.bibliographiccitation.volume","40"],["dc.contributor.author","Neubacher, Henrik"],["dc.contributor.author","Hoefer, Ines"],["dc.contributor.author","Meyenberg, Karsten"],["dc.contributor.author","Diederichsen, Ulf"],["dc.contributor.author","Steinem, Claudia"],["dc.date.accessioned","2018-11-07T08:53:34Z"],["dc.date.available","2018-11-07T08:53:34Z"],["dc.date.issued","2011"],["dc.identifier.isi","000293637300157"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/22445"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Springer"],["dc.publisher.place","New york"],["dc.relation.eventlocation","Budapest, Hungary"],["dc.relation.issn","0175-7571"],["dc.title","SNARE-mediated membrane fusion assay based on pore-suspending membranes: observing single fusion events"],["dc.type","conference_abstract"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details WOS