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Andreas Herrmann

Researcher at Humboldt University of Berlin

Publications -  371
Citations -  13813

Andreas Herrmann is an academic researcher from Humboldt University of Berlin. The author has contributed to research in topics: Membrane & Lipid bilayer fusion. The author has an hindex of 62, co-authored 369 publications receiving 12507 citations. Previous affiliations of Andreas Herrmann include Humboldt State University & Charité.

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Differential effects of PER2 phosphorylation: molecular basis for the human familial advanced sleep phase syndrome (FASPS)

TL;DR: Interference with specific aspects of mPER2 phosphorylation leads to either short or long periods in oscillating fibroblasts, which explains not only the FASPS phenotype, but also the effect of the tau mutation in hamster as well as the doubletime mutants (dbtS and dbtL ) in Drosophila.
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Live-cell analysis of cell penetration ability and toxicity of oligo-arginines.

TL;DR: Interestingly, the transduction difference between D‐ and L‐forms was highly variable between cell types, emphasizing the need for protease‐resistant peptides as vectors for drug delivery.
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Inhibition of Influenza Virus Infection by Multivalent Sialic‐Acid‐Functionalized Gold Nanoparticles

TL;DR: An efficient synthesis of sialic-acid-terminated glycerol dendron to chemically functionalize 2 nm and 14 nm gold nanoparticles (AuNPs) is described, which allows a new type of molecular-imaging activity-correlation and is of particular relevance for further application in alternative antiviral therapy.
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Lipidic pore formation by the concerted action of proapoptotic BAX and tBID

TL;DR: A novel model is proposed in which tBID assists BAX not only viaprotein-protein but also via protein-lipid interactions to form lipidic pore-type non-bilayer structures in the outer mitochondrial membrane through which intermembrane prodeath molecules exit mitochondria during apoptosis.
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Cell Entry of Arginine-rich Peptides Is Independent of Endocytosis *□

TL;DR: Although the frequency and kinetics of TAT transduction varied between cell types, it was independent of endocytosis and therefore results from TAT peptide that directly penetrated (transduced) the plasma membrane.