@article{51121,
  abstract     = {{<jats:p>DNA origami nanostructures are a powerful tool in biomedicine and can be used to combat drug‐resistant bacterial infections. However, the effect of unmodified DNA origami nanostructures on bacteria is yet to be elucidated. With the aim to obtain a better understanding of this phenomenon, the effect of three DNA origami shapes, i.e., DNA origami triangles, six‐helix bundles (6HBs), and 24‐helix bundles (24HBs), on the growth of Gram‐negative Escherichia coli and Gram‐positive Bacillus subtilis is investigated. These results reveal that while triangles and 24HBs can be used as a source of nutrients by E. coli and thereby promote population growth, their effect is much smaller than that of genomic single‐ and double‐stranded DNA. However, no effect on E. coli population growth is observed for the 6HBs. On the other hand, B. subtilis does not show any significant changes in population growth when cultured with the different DNA origami shapes or genomic DNA. The detailed effect of DNA origami nanostructures on bacterial growth thus depends on the competence signals and uptake mechanism of each bacterial species, as well as the DNA origami shape. This should be considered in the development of antimicrobial DNA origami nanostructures.</jats:p>}},
  author       = {{Garcia-Diosa, Jaime Andres and Grundmeier, Guido and Keller, Adrian}},
  issn         = {{1439-4227}},
  journal      = {{ChemBioChem}},
  keywords     = {{Organic Chemistry, Molecular Biology, Molecular Medicine, Biochemistry}},
  publisher    = {{Wiley}},
  title        = {{{Effect of DNA Origami Nanostructures on Bacterial Growth}}},
  doi          = {{10.1002/cbic.202400091}},
  year         = {{2024}},
}

@article{50150,
  abstract     = {{<jats:p>Covalent peptidomimetic protease inhibitors have gained a lot of attention in drug development in recent years. They are designed to covalently bind the catalytically active amino acids through electrophilic groups called warheads. Covalent inhibition has an advantage in terms of pharmacodynamic properties but can also bear toxicity risks due to non-selective off-target protein binding. Therefore, the right combination of a reactive warhead with a well-suited peptidomimetic sequence is of great importance. Herein, the selectivities of well-known warheads combined with peptidomimetic sequences suited for five different proteases were investigated, highlighting the impact of both structure parts (warhead and peptidomimetic sequence) for affinity and selectivity. Molecular docking gave insights into the predicted binding modes of the inhibitors inside the binding pockets of the different enzymes. Moreover, the warheads were investigated by NMR and LC-MS reactivity assays against serine/threonine and cysteine nucleophile models, as well as by quantum mechanics simulations.</jats:p>}},
  author       = {{Müller, Patrick and Meta, Mergim and Meidner, Jan Laurenz and Schwickert, Marvin and Meyr, Jessica and Schwickert, Kevin and Kersten, Christian and Zimmer, Collin and Hammerschmidt, Stefan Josef and Frey, Ariane and Lahu, Albin and de la Hoz-Rodríguez, Sergio and Agost-Beltrán, Laura and Rodríguez, Santiago and Diemer, Kira and Neumann, Wilhelm and Gonzàlez, Florenci V. and Engels, Bernd and Schirmeister, Tanja}},
  issn         = {{1422-0067}},
  journal      = {{International Journal of Molecular Sciences}},
  keywords     = {{Inorganic Chemistry, Organic Chemistry, Physical and Theoretical Chemistry, Computer Science Applications, Spectroscopy, Molecular Biology, General Medicine, Catalysis}},
  number       = {{8}},
  publisher    = {{MDPI AG}},
  title        = {{{Investigation of the Compatibility between Warheads and Peptidomimetic Sequences of Protease Inhibitors—A Comprehensive Reactivity and Selectivity Study}}},
  doi          = {{10.3390/ijms24087226}},
  volume       = {{24}},
  year         = {{2023}},
}

@article{35160,
  author       = {{Jia, Jichao and Cao, Xue and Ma, Xuekai and De, Jianbo and Yao, Jiannian and Schumacher, Stefan and Liao, Qing and Fu, Hongbing}},
  issn         = {{2041-1723}},
  journal      = {{Nature Communications}},
  keywords     = {{General Physics and Astronomy, General Biochemistry, Genetics and Molecular Biology, General Chemistry, Multidisciplinary}},
  number       = {{1}},
  publisher    = {{Springer Science and Business Media LLC}},
  title        = {{{Circularly polarized electroluminescence from a single-crystal organic microcavity light-emitting diode based on photonic spin-orbit interactions}}},
  doi          = {{10.1038/s41467-022-35745-w}},
  volume       = {{14}},
  year         = {{2023}},
}

@article{44503,
  author       = {{Hanke, Marcel and Tomm, Emilia and Grundmeier, Guido and Keller, Adrian}},
  issn         = {{1439-4227}},
  journal      = {{ChemBioChem}},
  keywords     = {{Organic Chemistry, Molecular Biology, Molecular Medicine, Biochemistry}},
  publisher    = {{Wiley}},
  title        = {{{Effect of Ionic Strength on the Thermal Stability of DNA Origami Nanostructures}}},
  doi          = {{10.1002/cbic.202300338}},
  year         = {{2023}},
}

@article{45868,
  abstract     = {{Perfect vector vortex beams (PVVBs) have attracted considerable interest due to their peculiar optical features. PVVBs are typically generated through the superposition of perfect vortex beams, which suffer from the limited number of topological charges (TCs). Furthermore, dynamic control of PVVBs is desirable and has not been reported. We propose and experimentally demonstrate hybrid grafted perfect vector vortex beams (GPVVBs) and their dynamic control. Hybrid GPVVBs are generated through the superposition of grafted perfect vortex beams with a multifunctional metasurface. The generated hybrid GPVVBs possess spatially variant rates of polarization change due to the involvement of more TCs. Each hybrid GPVVB includes different GPVVBs in the same beam, adding more design flexibility. Moreover, these beams are dynamically controlled with a rotating half waveplate. The generated dynamic GPVVBs may find applications in the fields where dynamic control is in high demand, including optical encryption, dense data communication, and multiple particle manipulation.}},
  author       = {{Ahmed, Hammad and Ansari, Muhammad Afnan and Li, Yan and Zentgraf, Thomas and Mehmood, Muhammad Qasim and Chen, Xianzhong}},
  issn         = {{2041-1723}},
  journal      = {{Nature Communications}},
  keywords     = {{General Physics and Astronomy, General Biochemistry, Genetics and Molecular Biology, General Chemistry, Multidisciplinary}},
  number       = {{1}},
  publisher    = {{Springer Science and Business Media LLC}},
  title        = {{{Dynamic control of hybrid grafted perfect vector vortex beams}}},
  doi          = {{10.1038/s41467-023-39599-8}},
  volume       = {{14}},
  year         = {{2023}},
}

@article{46543,
  abstract     = {{<jats:p>The influence of nanoscale surface topography on protein adsorption is highly important for numerous applications in medicine and technology. Herein, ferritin adsorption at flat and nanofaceted, single-crystalline Al2O3 surfaces is investigated using atomic force microscopy and X-ray photoelectron spectroscopy. The nanofaceted surfaces are generated by the thermal annealing of Al2O3 wafers at temperatures above 1000 °C, which leads to the formation of faceted saw-tooth-like surface topographies with periodicities of about 160 nm and amplitudes of about 15 nm. Ferritin adsorption at these nanofaceted surfaces is notably suppressed compared to the flat surface at a concentration of 10 mg/mL, which is attributed to lower adsorption affinities of the newly formed facets. Consequently, adsorption is restricted mostly to the pattern grooves, where the proteins can maximize their contact area with the surface. However, this effect depends on the protein concentration, with an inverse trend being observed at 30 mg/mL. Furthermore, different ferritin adsorption behavior is observed at topographically similar nanofacet patterns fabricated at different annealing temperatures and attributed to different step and kink densities. These results demonstrate that while protein adsorption at solid surfaces can be notably affected by nanofacet patterns, fine-tuning protein adsorption in this way requires the precise control of facet properties.</jats:p>}},
  author       = {{Pothineni, Bhanu K. and Kollmann, Sabrina and Li, Xinyang and Grundmeier, Guido and Erb, Denise J. and Keller, Adrian}},
  issn         = {{1422-0067}},
  journal      = {{International Journal of Molecular Sciences}},
  keywords     = {{Inorganic Chemistry, Organic Chemistry, Physical and Theoretical Chemistry, Computer Science Applications, Spectroscopy, Molecular Biology, General Medicine, Catalysis}},
  number       = {{16}},
  publisher    = {{MDPI AG}},
  title        = {{{Adsorption of Ferritin at Nanofaceted Al2O3 Surfaces}}},
  doi          = {{10.3390/ijms241612808}},
  volume       = {{24}},
  year         = {{2023}},
}

@article{30209,
  abstract     = {{<jats:p>DNA origami technology enables the folding of DNA strands into complex nanoscale shapes whose properties and interactions with molecular species often deviate significantly from that of genomic DNA. Here, we investigate the salting-out of different DNA origami shapes by the kosmotropic salt ammonium sulfate that is routinely employed in protein precipitation. We find that centrifugation in the presence of 3 M ammonium sulfate results in notable precipitation of DNA origami nanostructures but not of double-stranded genomic DNA. The precipitated DNA origami nanostructures can be resuspended in ammonium sulfate-free buffer without apparent formation of aggregates or loss of structural integrity. Even though quasi-1D six-helix bundle DNA origami are slightly less susceptible toward salting-out than more compact DNA origami triangles and 24-helix bundles, precipitation and recovery yields appear to be mostly independent of DNA origami shape and superstructure. Exploiting the specificity of ammonium sulfate salting-out for DNA origami nanostructures, we further apply this method to separate DNA origami triangles from genomic DNA fragments in a complex mixture. Our results thus demonstrate the possibility of concentrating and purifying DNA origami nanostructures by ammonium sulfate-induced salting-out.</jats:p>}},
  author       = {{Hanke, Marcel and Hansen, Niklas and Chen, Ruiping and Grundmeier, Guido and Fahmy, Karim and Keller, Adrian}},
  issn         = {{1422-0067}},
  journal      = {{International Journal of Molecular Sciences}},
  keywords     = {{Inorganic Chemistry, Organic Chemistry, Physical and Theoretical Chemistry, Computer Science Applications, Spectroscopy, Molecular Biology, General Medicine, Catalysis}},
  number       = {{5}},
  pages        = {{2817}},
  publisher    = {{MDPI AG}},
  title        = {{{Salting-Out of DNA Origami Nanostructures by Ammonium Sulfate}}},
  doi          = {{10.3390/ijms23052817}},
  volume       = {{23}},
  year         = {{2022}},
}

@article{30385,
  abstract     = {{<jats:title>Abstract</jats:title><jats:p>Tailored nanoscale quantum light sources, matching the specific needs of use cases, are crucial building blocks for photonic quantum technologies. Several different approaches to realize solid-state quantum emitters with high performance have been pursued and different concepts for energy tuning have been established. However, the properties of the emitted photons are always defined by the individual quantum emitter and can therefore not be controlled with full flexibility. Here we introduce an all-optical nonlinear method to tailor and control the single photon emission. We demonstrate a laser-controlled down-conversion process from an excited state of a semiconductor quantum three-level system. Based on this concept, we realize energy tuning and polarization control of the single photon emission with a control-laser field. Our results mark an important step towards tailored single photon emission from a photonic quantum system based on quantum optical principles.</jats:p>}},
  author       = {{Jonas, B. and Heinze, D. and Schöll, E. and Kallert, P. and Langer, T. and Krehs, S. and Widhalm, A. and Jöns, K. D. and Reuter, D. and Schumacher, S. and Zrenner, Artur}},
  issn         = {{2041-1723}},
  journal      = {{Nature Communications}},
  keywords     = {{General Physics and Astronomy, General Biochemistry, Genetics and Molecular Biology, General Chemistry}},
  number       = {{1}},
  publisher    = {{Springer Science and Business Media LLC}},
  title        = {{{Nonlinear down-conversion in a single quantum dot}}},
  doi          = {{10.1038/s41467-022-28993-3}},
  volume       = {{13}},
  year         = {{2022}},
}

@article{29902,
  author       = {{Reineke Matsudo, Bernhard and Sain, Basudeb and Carletti, Luca and Zhang, Xue and Gao, Wenlong and Angelis, Costantino and Huang, Lingling and Zentgraf, Thomas}},
  issn         = {{2198-3844}},
  journal      = {{Advanced Science}},
  keywords     = {{General Physics and Astronomy, General Engineering, Biochemistry, Genetics and Molecular Biology (miscellaneous), General Materials Science, General Chemical Engineering, Medicine (miscellaneous)}},
  number       = {{12}},
  publisher    = {{Wiley}},
  title        = {{{Efficient Frequency Conversion with Geometric Phase Control in Optical Metasurfaces}}},
  doi          = {{10.1002/advs.202104508}},
  volume       = {{9}},
  year         = {{2022}},
}

@article{32589,
  abstract     = {{<jats:p>Guanidinium (Gdm) undergoes interactions with both hydrophilic and hydrophobic groups and, thus, is a highly potent denaturant of biomolecular structure. However, our molecular understanding of the interaction of Gdm with proteins and DNA is still rather limited. Here, we investigated the denaturation of DNA origami nanostructures by three Gdm salts, i.e., guanidinium chloride (GdmCl), guanidinium sulfate (Gdm2SO4), and guanidinium thiocyanate (GdmSCN), at different temperatures and in dependence of incubation time. Using DNA origami nanostructures as sensors that translate small molecular transitions into nanostructural changes, the denaturing effects of the Gdm salts were directly visualized by atomic force microscopy. GdmSCN was the most potent DNA denaturant, which caused complete DNA origami denaturation at 50 °C already at a concentration of 2 M. Under such harsh conditions, denaturation occurred within the first 15 min of Gdm exposure, whereas much slower kinetics were observed for the more weakly denaturing salt Gdm2SO4 at 25 °C. Lastly, we observed a novel non-monotonous temperature dependence of DNA origami denaturation in Gdm2SO4 with the fraction of intact nanostructures having an intermediate minimum at about 40 °C. Our results, thus, provide further insights into the highly complex Gdm–DNA interaction and underscore the importance of the counteranion species.</jats:p>}},
  author       = {{Hanke, Marcel and Hansen, Niklas and Tomm, Emilia and Grundmeier, Guido and Keller, Adrian}},
  issn         = {{1422-0067}},
  journal      = {{International Journal of Molecular Sciences}},
  keywords     = {{Inorganic Chemistry, Organic Chemistry, Physical and Theoretical Chemistry, Computer Science Applications, Spectroscopy, Molecular Biology, General Medicine, Catalysis}},
  number       = {{15}},
  pages        = {{8547}},
  publisher    = {{MDPI AG}},
  title        = {{{Time-Dependent DNA Origami Denaturation by Guanidinium Chloride, Guanidinium Sulfate, and Guanidinium Thiocyanate}}},
  doi          = {{10.3390/ijms23158547}},
  volume       = {{23}},
  year         = {{2022}},
}

@article{32877,
  author       = {{Gaidai, Roman and Gölz, Christian Johannes and Mora, K. and Rudisch, J. and Reuter, E.-M. and Godde, B. and Reinsberger, C. and Voelcker-Rehage, C. and Vieluf, S.}},
  issn         = {{0006-8993}},
  journal      = {{Brain Research}},
  keywords     = {{Developmental Biology, Neurology (clinical), Molecular Biology, General Neuroscience}},
  publisher    = {{Elsevier BV}},
  title        = {{{Classification characteristics of fine motor experts based on electroencephalographic and force tracking data}}},
  doi          = {{10.1016/j.brainres.2022.148001}},
  volume       = {{1792}},
  year         = {{2022}},
}

@article{33833,
  author       = {{Kim, Sanghoon and Pathak, Sachin and Rhim, Sonny H. and Cha, Jongin and Jekal, Soyoung and Hong, Soon Cheol and Lee, Hyun Hwi and Park, Sung‐Hun and Lee, Han‐Koo and Park, Jae‐Hoon and Lee, Soogil and Steinrück, Hans-Georg and Mehta, Apurva and Wang, Shan X. and Hong, Jongill}},
  issn         = {{2198-3844}},
  journal      = {{Advanced Science}},
  keywords     = {{General Physics and Astronomy, General Engineering, Biochemistry, Genetics and Molecular Biology (miscellaneous), General Materials Science, General Chemical Engineering, Medicine (miscellaneous)}},
  number       = {{24}},
  pages        = {{2201749}},
  publisher    = {{Wiley}},
  title        = {{{Giant Orbital Anisotropy with Strong Spin–Orbit Coupling Established at the Pseudomorphic Interface of the Co/Pd Superlattice}}},
  doi          = {{10.1002/advs.202201749}},
  volume       = {{9}},
  year         = {{2022}},
}

@article{40523,
  abstract     = {{<jats:title>Abstract</jats:title><jats:p>Tailored nanoscale quantum light sources, matching the specific needs of use cases, are crucial building blocks for photonic quantum technologies. Several different approaches to realize solid-state quantum emitters with high performance have been pursued and different concepts for energy tuning have been established. However, the properties of the emitted photons are always defined by the individual quantum emitter and can therefore not be controlled with full flexibility. Here we introduce an all-optical nonlinear method to tailor and control the single photon emission. We demonstrate a laser-controlled down-conversion process from an excited state of a semiconductor quantum three-level system. Based on this concept, we realize energy tuning and polarization control of the single photon emission with a control-laser field. Our results mark an important step towards tailored single photon emission from a photonic quantum system based on quantum optical principles.</jats:p>}},
  author       = {{Jonas, B. and Heinze, Dirk Florian and Schöll, E. and Kallert, P. and Langer, T. and Krehs, S. and Widhalm, A. and Jöns, Klaus and Reuter, Dirk and Schumacher, Stefan and Zrenner, Artur}},
  issn         = {{2041-1723}},
  journal      = {{Nature Communications}},
  keywords     = {{General Physics and Astronomy, General Biochemistry, Genetics and Molecular Biology, General Chemistry, Multidisciplinary}},
  number       = {{1}},
  publisher    = {{Springer Science and Business Media LLC}},
  title        = {{{Nonlinear down-conversion in a single quantum dot}}},
  doi          = {{10.1038/s41467-022-28993-3}},
  volume       = {{13}},
  year         = {{2022}},
}

@article{33080,
  author       = {{Long, Teng and Ma, Xuekai and Ren, Jiahuan and Li, Feng and Liao, Qing and Schumacher, Stefan and Malpuech, Guillaume and Solnyshkov, Dmitry and Fu, Hongbing}},
  issn         = {{2198-3844}},
  journal      = {{Advanced Science}},
  keywords     = {{General Physics and Astronomy, General Engineering, Biochemistry, Genetics and Molecular Biology (miscellaneous), General Materials Science, General Chemical Engineering, Medicine (miscellaneous)}},
  number       = {{29}},
  publisher    = {{Wiley}},
  title        = {{{Helical Polariton Lasing from Topological Valleys in an Organic Crystalline Microcavity}}},
  doi          = {{10.1002/advs.202203588}},
  volume       = {{9}},
  year         = {{2022}},
}

@article{32310,
  author       = {{Li, Yao and Ma, Xuekai and Zhai, Xiaokun and Gao, Meini and Dai, Haitao and Schumacher, Stefan and Gao, Tingge}},
  issn         = {{2041-1723}},
  journal      = {{Nature Communications}},
  keywords     = {{General Physics and Astronomy, General Biochemistry, Genetics and Molecular Biology, General Chemistry, Multidisciplinary}},
  number       = {{1}},
  publisher    = {{Springer Science and Business Media LLC}},
  title        = {{{Manipulating polariton condensates by Rashba-Dresselhaus coupling at room temperature}}},
  doi          = {{10.1038/s41467-022-31529-4}},
  volume       = {{13}},
  year         = {{2022}},
}

@article{37338,
  abstract     = {{<jats:title>Abstract</jats:title><jats:p>Methylammonium lead iodide perovskite (MAPbI<jats:sub>3</jats:sub>) is renowned for an impressive power conversion efficiency rise and cost-effective fabrication for photovoltaics. In this work, we demonstrate that polycrystalline MAPbI<jats:sub>3</jats:sub>s undergo drastic changes in optical properties at moderate field strengths with an ultrafast response time, via transient Wannier Stark localization. The distinct band structure of this material - the large lattice periodicity, the narrow electronic energy bandwidths, and the coincidence of these two along the same high-symmetry direction – enables relatively weak fields to bring this material into the Wannier Stark regime. Its polycrystalline nature is not detrimental to the optical switching performance of the material, since the least dispersive direction of the band structure dominates the contribution to the optical response, which favors low-cost fabrication. Together with the outstanding photophysical properties of MAPbI<jats:sub>3</jats:sub>, this finding highlights the great potential of this material in ultrafast light modulation and novel photonic applications.</jats:p>}},
  author       = {{Berghoff, Daniel and Bühler, Johannes and Bonn, Mischa and Leitenstorfer, Alfred and Meier, Torsten and Kim, Heejae}},
  issn         = {{2041-1723}},
  journal      = {{Nature Communications}},
  keywords     = {{General Physics and Astronomy, General Biochemistry, Genetics and Molecular Biology, General Chemistry, Multidisciplinary}},
  number       = {{1}},
  publisher    = {{Springer Science and Business Media LLC}},
  title        = {{{Low-field onset of Wannier-Stark localization in a polycrystalline hybrid organic inorganic perovskite}}},
  doi          = {{10.1038/s41467-021-26021-4}},
  volume       = {{12}},
  year         = {{2021}},
}

@article{40577,
  author       = {{Tian, Zhihong and Lopez Salas, Nieves and Liu, Chuntai and Liu, Tianxi and Antonietti, Markus}},
  issn         = {{2198-3844}},
  journal      = {{Advanced Science}},
  keywords     = {{General Physics and Astronomy, General Engineering, Biochemistry, Genetics and Molecular Biology (miscellaneous), General Materials Science, General Chemical Engineering, Medicine (miscellaneous)}},
  number       = {{24}},
  publisher    = {{Wiley}},
  title        = {{{C            <sub>2</sub>            N: A Class of Covalent Frameworks with Unique Properties}}},
  doi          = {{10.1002/advs.202001767}},
  volume       = {{7}},
  year         = {{2020}},
}

@article{41023,
  abstract     = {{<jats:title>Abstract</jats:title><jats:p>Efficient oxygen evolution reaction (OER) electrocatalysts are pivotal for sustainable fuel production, where the Ni-Fe oxyhydroxide (OOH) is among the most active catalysts for alkaline OER. Electrolyte alkali metal cations have been shown to modify the activity and reaction intermediates, however, the exact mechanism is at question due to unexplained deviations from the cation size trend. Our X-ray absorption spectroelectrochemical results show that bigger cations shift the Ni<jats:sup>2+/(3+δ)+</jats:sup> redox peak and OER activity to lower potentials (however, with typical discrepancies), following the order CsOH &gt; NaOH ≈ KOH &gt; RbOH &gt; LiOH. Here, we find that the OER activity follows the variations in electrolyte pH rather than a specific cation, which accounts for differences both in basicity of the alkali hydroxides and other contributing anomalies. Our density functional theory-derived reactivity descriptors confirm that cations impose negligible effect on the Lewis acidity of Ni, Fe, and O lattice sites, thus strengthening the conclusions of an indirect pH effect.</jats:p>}},
  author       = {{Görlin, Mikaela and Halldin Stenlid, Joakim and Koroidov, Sergey and Wang, Hsin-Yi and Börner, Mia and Shipilin, Mikhail and Kalinko, Aleksandr and Murzin, Vadim and Safonova, Olga V. and Nachtegaal, Maarten and Uheida, Abdusalam and Dutta, Joydeep and Bauer, Matthias and Nilsson, Anders and Diaz-Morales, Oscar}},
  issn         = {{2041-1723}},
  journal      = {{Nature Communications}},
  keywords     = {{General Physics and Astronomy, General Biochemistry, Genetics and Molecular Biology, General Chemistry, Multidisciplinary}},
  number       = {{1}},
  publisher    = {{Springer Science and Business Media LLC}},
  title        = {{{Key activity descriptors of nickel-iron oxygen evolution electrocatalysts in the presence of alkali metal cations}}},
  doi          = {{10.1038/s41467-020-19729-2}},
  volume       = {{11}},
  year         = {{2020}},
}

@article{41821,
  author       = {{Sistemich, Linda and Kutsch, Miriam and Hämisch, Benjamin and Zhang, Ping and Shydlovskyi, Sergii and Britzen-Laurent, Nathalie and Stürzl, Michael and Huber, Klaus and Herrmann, Christian}},
  issn         = {{0022-2836}},
  journal      = {{Journal of Molecular Biology}},
  keywords     = {{Molecular Biology, Structural Biology}},
  number       = {{7}},
  pages        = {{2164--2185}},
  publisher    = {{Elsevier BV}},
  title        = {{{The Molecular Mechanism of Polymer Formation of Farnesylated Human Guanylate-binding Protein 1}}},
  doi          = {{10.1016/j.jmb.2020.02.009}},
  volume       = {{432}},
  year         = {{2020}},
}

@article{41054,
  author       = {{Jagadeesh, Rajenahally V and Stemmler, Tobias and Surkus, Annette-Enrica and Bauer, Matthias and Pohl, Marga-Martina and Radnik, Jörg and Junge, Kathrin and Junge, Henrik and Brückner, Angelika and Beller, Matthias}},
  issn         = {{1754-2189}},
  journal      = {{Nature Protocols}},
  keywords     = {{General Biochemistry, Genetics and Molecular Biology}},
  number       = {{6}},
  pages        = {{916--926}},
  publisher    = {{Springer Science and Business Media LLC}},
  title        = {{{Cobalt-based nanocatalysts for green oxidation and hydrogenation processes}}},
  doi          = {{10.1038/nprot.2015.049}},
  volume       = {{10}},
  year         = {{2015}},
}