H. Bauke Albada
Hebrew University of Jerusalem
34 Papers
207 Citations
H. Bauke Albada is an academic researcher from Hebrew University of Jerusalem. The author has contributed to research in topics: Antimicrobial peptides & Peptide. The author has an hindex of 20, co-authored 34 publications. Previous affiliations of H. Bauke Albada include Utrecht University & Ruhr University Bochum.
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Papers
Multifunctional, defect-engineered metal-organic frameworks with ruthenium centers: sorption and catalytic properties.
Olesia Kozachuk,Ignacio Luz,Francesc X. Llabrés i Xamena,Heshmat Noei,Max Kauer,H. Bauke Albada,Eric D. Bloch,Bernd Marler,Yuemin Wang,Martin Muhler,Roland A. Fischer +10 more
TL;DR: The modified Ru sites are responsible for the activity of the "defective" variants in the dissociative chemisorption of CO2, the enhanced performance in CO sorption, the formation of hydride species, and the catalytic hydrogenation of olefins.
Nucleoapzymes: Hemin/G-Quadruplex DNAzyme–Aptamer Binding Site Conjugates with Superior Enzyme-like Catalytic Functions
TL;DR: All nucleoapzymes reveal enhanced catalytic activities as compared to the separated DNAzyme/aptamer units, and the most activeucleoapzyme reveals a 20-fold enhanced activity.
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Tuning the activity of a short arg-trp antimicrobial Peptide by lipidation of a C- or N-terminal lysine side-chain.
H. Bauke Albada,Pascal Prochnow,Sandra Bobersky,Sina Langklotz,Patrick Schriek,Julia E. Bandow,Nils Metzler-Nolte +6 more
TL;DR: The attachment of lipids to C- or N-terminally positioned lysine side-chain amino groups increases the activity of a short synthetic (Arg-Trp)3 antimicrobial peptide significantly, making these peptides even active against pathogenic Gram-negative bacteria.
Modulating the activity of short arginine-tryptophan containing antibacterial peptides with N-terminal metallocenoyl groups
H. Bauke Albada,Alina-Iulia Chiriac,Michaela Wenzel,Maya Penkova,Julia E. Bandow,Hans-Georg Sahl,Nils Metzler-Nolte +6 more
TL;DR: Both the killing kinetics and growth inhibition studies presented in this work point to a membrane-based mode of action for these two peptides, each having different kinetic parameters.
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Computational docking simulations of a DNA-aptamer for argininamide and related ligands
TL;DR: Docking simulations are applied to probe the features of an experimentally documented L-argininamide aptamer complex to provide valuable guidelines for the application of docking simulations for the prediction of aptamer-ligand structures, and for the design of novel features of ligand-aptamer complexes.
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