--- _id: '14770' abstract: - lang: eng text: We developed LIONESS, a technology that leverages improvements to optical super-resolution microscopy and prior information on sample structure via machine learning to overcome the limitations (in 3D-resolution, signal-to-noise ratio and light exposure) of optical microscopy of living biological specimens. LIONESS enables dense reconstruction of living brain tissue and morphodynamics visualization at the nanoscale. article_processing_charge: No article_type: letter_note author: - first_name: Johann G full_name: Danzl, Johann G id: 42EFD3B6-F248-11E8-B48F-1D18A9856A87 last_name: Danzl orcid: 0000-0001-8559-3973 - first_name: Philipp full_name: Velicky, Philipp id: 39BDC62C-F248-11E8-B48F-1D18A9856A87 last_name: Velicky orcid: 0000-0002-2340-7431 citation: ama: Danzl JG, Velicky P. LIONESS enables 4D nanoscale reconstruction of living brain tissue. Nature Methods. 2023;20(8):1141-1142. doi:10.1038/s41592-023-01937-5 apa: Danzl, J. G., & Velicky, P. (2023). LIONESS enables 4D nanoscale reconstruction of living brain tissue. Nature Methods. Springer Nature. https://doi.org/10.1038/s41592-023-01937-5 chicago: Danzl, Johann G, and Philipp Velicky. “LIONESS Enables 4D Nanoscale Reconstruction of Living Brain Tissue.” Nature Methods. Springer Nature, 2023. https://doi.org/10.1038/s41592-023-01937-5. ieee: J. G. Danzl and P. Velicky, “LIONESS enables 4D nanoscale reconstruction of living brain tissue,” Nature Methods, vol. 20, no. 8. Springer Nature, pp. 1141–1142, 2023. ista: Danzl JG, Velicky P. 2023. LIONESS enables 4D nanoscale reconstruction of living brain tissue. Nature Methods. 20(8), 1141–1142. mla: Danzl, Johann G., and Philipp Velicky. “LIONESS Enables 4D Nanoscale Reconstruction of Living Brain Tissue.” Nature Methods, vol. 20, no. 8, Springer Nature, 2023, pp. 1141–42, doi:10.1038/s41592-023-01937-5. short: J.G. Danzl, P. Velicky, Nature Methods 20 (2023) 1141–1142. date_created: 2024-01-10T08:07:15Z date_published: 2023-08-01T00:00:00Z date_updated: 2024-01-10T08:37:48Z day: '01' department: - _id: JoDa doi: 10.1038/s41592-023-01937-5 external_id: isi: - '001025621500002' intvolume: ' 20' isi: 1 issue: '8' keyword: - Cell Biology - Molecular Biology - Biochemistry - Biotechnology language: - iso: eng month: '08' oa_version: None page: 1141-1142 publication: Nature Methods publication_identifier: eissn: - 1548-7105 issn: - 1548-7091 publication_status: published publisher: Springer Nature quality_controlled: '1' related_material: record: - id: '13267' relation: extended_version status: public scopus_import: '1' status: public title: LIONESS enables 4D nanoscale reconstruction of living brain tissue type: journal_article user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 20 year: '2023' ... --- _id: '15144' article_processing_charge: No article_type: letter_note author: - first_name: Jack Peter Kelly full_name: Bravo, Jack Peter Kelly id: 96aecfa5-8931-11ee-af30-aa6a5d6eee0e last_name: Bravo orcid: 0000-0003-0456-0753 citation: ama: Bravo JPK. SuperFi-Cas9 exceeds fidelity, matches speed of original Cas9. Genetic Engineering & Biotechnology News. 2022;42(4):12. doi:10.1089/gen.42.04.03 apa: Bravo, J. P. K. (2022). SuperFi-Cas9 exceeds fidelity, matches speed of original Cas9. Genetic Engineering & Biotechnology News. Mary Ann Liebert. https://doi.org/10.1089/gen.42.04.03 chicago: Bravo, Jack Peter Kelly. “SuperFi-Cas9 Exceeds Fidelity, Matches Speed of Original Cas9.” Genetic Engineering & Biotechnology News. Mary Ann Liebert, 2022. https://doi.org/10.1089/gen.42.04.03. ieee: J. P. K. Bravo, “SuperFi-Cas9 exceeds fidelity, matches speed of original Cas9,” Genetic Engineering & Biotechnology News, vol. 42, no. 4. Mary Ann Liebert, p. 12, 2022. ista: Bravo JPK. 2022. SuperFi-Cas9 exceeds fidelity, matches speed of original Cas9. Genetic Engineering & Biotechnology News. 42(4), 12. mla: Bravo, Jack Peter Kelly. “SuperFi-Cas9 Exceeds Fidelity, Matches Speed of Original Cas9.” Genetic Engineering & Biotechnology News, vol. 42, no. 4, Mary Ann Liebert, 2022, p. 12, doi:10.1089/gen.42.04.03. short: J.P.K. Bravo, Genetic Engineering & Biotechnology News 42 (2022) 12. date_created: 2024-03-20T10:43:19Z date_published: 2022-04-01T00:00:00Z date_updated: 2024-03-20T10:58:33Z day: '01' doi: 10.1089/gen.42.04.03 extern: '1' intvolume: ' 42' issue: '4' keyword: - Management of Technology and Innovation - Biomedical Engineering - Bioengineering - Biotechnology language: - iso: eng month: '04' oa_version: None page: '12' publication: Genetic Engineering & Biotechnology News publication_identifier: eissn: - 1937-8661 issn: - 1935-472X publication_status: published publisher: Mary Ann Liebert quality_controlled: '1' scopus_import: '1' status: public title: SuperFi-Cas9 exceeds fidelity, matches speed of original Cas9 type: journal_article user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 42 year: '2022' ... --- _id: '8402' abstract: - lang: eng text: "Background: The mitochondrial pyruvate carrier (MPC) plays a central role in energy metabolism by transporting pyruvate across the inner mitochondrial membrane. Its heterodimeric composition and homology to SWEET and semiSWEET transporters set the MPC apart from the canonical mitochondrial carrier family (named MCF or SLC25). The import of the canonical carriers is mediated by the carrier translocase of the inner membrane (TIM22) pathway and is dependent on their structure, which features an even number of transmembrane segments and both termini in the intermembrane space. The import pathway of MPC proteins has not been elucidated. The odd number of transmembrane segments and positioning of the N-terminus in the matrix argues against an import via the TIM22 carrier pathway but favors an import via the flexible presequence pathway.\r\nResults: Here, we systematically analyzed the import pathways of Mpc2 and Mpc3 and report that, contrary to an expected import via the flexible presequence pathway, yeast MPC proteins with an odd number of transmembrane segments and matrix-exposed N-terminus are imported by the carrier pathway, using the receptor Tom70, small TIM chaperones, and the TIM22 complex. The TIM9·10 complex chaperones MPC proteins through the mitochondrial intermembrane space using conserved hydrophobic motifs that are also required for the interaction with canonical carrier proteins.\r\nConclusions: The carrier pathway can import paired and non-paired transmembrane helices and translocate N-termini to either side of the mitochondrial inner membrane, revealing an unexpected versatility of the mitochondrial import pathway for non-cleavable inner membrane proteins." article_number: '2' article_processing_charge: No article_type: original author: - first_name: Heike full_name: Rampelt, Heike last_name: Rampelt - first_name: Iva full_name: Sucec, Iva last_name: Sucec - first_name: Beate full_name: Bersch, Beate last_name: Bersch - first_name: Patrick full_name: Horten, Patrick last_name: Horten - first_name: Inge full_name: Perschil, Inge last_name: Perschil - first_name: Jean-Claude full_name: Martinou, Jean-Claude last_name: Martinou - first_name: Martin full_name: van der Laan, Martin last_name: van der Laan - first_name: Nils full_name: Wiedemann, Nils last_name: Wiedemann - first_name: Paul full_name: Schanda, Paul id: 7B541462-FAF6-11E9-A490-E8DFE5697425 last_name: Schanda orcid: 0000-0002-9350-7606 - first_name: Nikolaus full_name: Pfanner, Nikolaus last_name: Pfanner citation: ama: Rampelt H, Sucec I, Bersch B, et al. The mitochondrial carrier pathway transports non-canonical substrates with an odd number of transmembrane segments. BMC Biology. 2020;18. doi:10.1186/s12915-019-0733-6 apa: Rampelt, H., Sucec, I., Bersch, B., Horten, P., Perschil, I., Martinou, J.-C., … Pfanner, N. (2020). The mitochondrial carrier pathway transports non-canonical substrates with an odd number of transmembrane segments. BMC Biology. Springer Nature. https://doi.org/10.1186/s12915-019-0733-6 chicago: Rampelt, Heike, Iva Sucec, Beate Bersch, Patrick Horten, Inge Perschil, Jean-Claude Martinou, Martin van der Laan, Nils Wiedemann, Paul Schanda, and Nikolaus Pfanner. “The Mitochondrial Carrier Pathway Transports Non-Canonical Substrates with an Odd Number of Transmembrane Segments.” BMC Biology. Springer Nature, 2020. https://doi.org/10.1186/s12915-019-0733-6. ieee: H. Rampelt et al., “The mitochondrial carrier pathway transports non-canonical substrates with an odd number of transmembrane segments,” BMC Biology, vol. 18. Springer Nature, 2020. ista: Rampelt H, Sucec I, Bersch B, Horten P, Perschil I, Martinou J-C, van der Laan M, Wiedemann N, Schanda P, Pfanner N. 2020. The mitochondrial carrier pathway transports non-canonical substrates with an odd number of transmembrane segments. BMC Biology. 18, 2. mla: Rampelt, Heike, et al. “The Mitochondrial Carrier Pathway Transports Non-Canonical Substrates with an Odd Number of Transmembrane Segments.” BMC Biology, vol. 18, 2, Springer Nature, 2020, doi:10.1186/s12915-019-0733-6. short: H. Rampelt, I. Sucec, B. Bersch, P. Horten, I. Perschil, J.-C. Martinou, M. van der Laan, N. Wiedemann, P. Schanda, N. Pfanner, BMC Biology 18 (2020). date_created: 2020-09-17T10:26:53Z date_published: 2020-01-06T00:00:00Z date_updated: 2021-01-12T08:19:02Z day: '06' doi: 10.1186/s12915-019-0733-6 extern: '1' external_id: pmid: - '31907035' intvolume: ' 18' keyword: - Biotechnology - Plant Science - General Biochemistry - Genetics and Molecular Biology - Developmental Biology - Cell Biology - Physiology - Ecology - Evolution - Behavior and Systematics - Structural Biology - General Agricultural and Biological Sciences language: - iso: eng main_file_link: - open_access: '1' url: https://doi.org/10.1186/s12915-019-0733-6 month: '01' oa: 1 oa_version: Published Version pmid: 1 publication: BMC Biology publication_identifier: issn: - 1741-7007 publication_status: published publisher: Springer Nature quality_controlled: '1' status: public title: The mitochondrial carrier pathway transports non-canonical substrates with an odd number of transmembrane segments type: journal_article user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 18 year: '2020' ... --- _id: '13363' abstract: - lang: eng text: Temporal activation of biological processes by visible light and subsequent return to an inactive state in the absence of light is an essential characteristic of photoreceptor cells. Inspired by these phenomena, light-responsive materials are very attractive due to the high spatiotemporal control of light irradiation, with light being able to precisely orchestrate processes repeatedly over many cycles. Herein, it is reported that light-driven proton transfer triggered by a merocyanine-based photoacid can be used to modulate the permeability of pH-responsive polymersomes through cyclic, temporally controlled protonation and deprotonation of the polymersome membrane. The membranes can undergo repeated light-driven swelling–contraction cycles without losing functional effectiveness. When applied to enzyme loaded-nanoreactors, this membrane responsiveness is used for the reversible control of enzymatic reactions. This combination of the merocyanine-based photoacid and pH-switchable nanoreactors results in rapidly responding and versatile supramolecular systems successfully used to switch enzymatic reactions ON and OFF on demand. article_number: '2002135' article_processing_charge: No article_type: original author: - first_name: Silvia full_name: Moreno, Silvia last_name: Moreno - first_name: Priyanka full_name: Sharan, Priyanka last_name: Sharan - first_name: Johanna full_name: Engelke, Johanna last_name: Engelke - first_name: Hannes full_name: Gumz, Hannes last_name: Gumz - first_name: Susanne full_name: Boye, Susanne last_name: Boye - first_name: Ulrich full_name: Oertel, Ulrich last_name: Oertel - first_name: Peng full_name: Wang, Peng last_name: Wang - first_name: Susanta full_name: Banerjee, Susanta last_name: Banerjee - first_name: Rafal full_name: Klajn, Rafal id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b last_name: Klajn - first_name: Brigitte full_name: Voit, Brigitte last_name: Voit - first_name: Albena full_name: Lederer, Albena last_name: Lederer - first_name: Dietmar full_name: Appelhans, Dietmar last_name: Appelhans citation: ama: Moreno S, Sharan P, Engelke J, et al. Light‐driven proton transfer for cyclic and temporal switching of enzymatic nanoreactors. Small. 2020;16(37). doi:10.1002/smll.202002135 apa: Moreno, S., Sharan, P., Engelke, J., Gumz, H., Boye, S., Oertel, U., … Appelhans, D. (2020). Light‐driven proton transfer for cyclic and temporal switching of enzymatic nanoreactors. Small. Wiley. https://doi.org/10.1002/smll.202002135 chicago: Moreno, Silvia, Priyanka Sharan, Johanna Engelke, Hannes Gumz, Susanne Boye, Ulrich Oertel, Peng Wang, et al. “Light‐driven Proton Transfer for Cyclic and Temporal Switching of Enzymatic Nanoreactors.” Small. Wiley, 2020. https://doi.org/10.1002/smll.202002135. ieee: S. Moreno et al., “Light‐driven proton transfer for cyclic and temporal switching of enzymatic nanoreactors,” Small, vol. 16, no. 37. Wiley, 2020. ista: Moreno S, Sharan P, Engelke J, Gumz H, Boye S, Oertel U, Wang P, Banerjee S, Klajn R, Voit B, Lederer A, Appelhans D. 2020. Light‐driven proton transfer for cyclic and temporal switching of enzymatic nanoreactors. Small. 16(37), 2002135. mla: Moreno, Silvia, et al. “Light‐driven Proton Transfer for Cyclic and Temporal Switching of Enzymatic Nanoreactors.” Small, vol. 16, no. 37, 2002135, Wiley, 2020, doi:10.1002/smll.202002135. short: S. Moreno, P. Sharan, J. Engelke, H. Gumz, S. Boye, U. Oertel, P. Wang, S. Banerjee, R. Klajn, B. Voit, A. Lederer, D. Appelhans, Small 16 (2020). date_created: 2023-08-01T09:36:48Z date_published: 2020-08-11T00:00:00Z date_updated: 2023-08-07T10:11:41Z day: '11' doi: 10.1002/smll.202002135 extern: '1' external_id: pmid: - '32783385' intvolume: ' 16' issue: '37' keyword: - Biomaterials - Biotechnology - General Materials Science - General Chemistry language: - iso: eng main_file_link: - open_access: '1' url: https://doi.org/10.1002/smll.202002135 month: '08' oa: 1 oa_version: Published Version pmid: 1 publication: Small publication_identifier: eissn: - 1613-6829 issn: - 1613-6810 publication_status: published publisher: Wiley quality_controlled: '1' scopus_import: '1' status: public title: Light‐driven proton transfer for cyclic and temporal switching of enzymatic nanoreactors type: journal_article user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 16 year: '2020' ... --- _id: '14286' abstract: - lang: eng text: 'The bacteriophage M13 has found frequent applications in nanobiotechnology due to its chemically and genetically tunable protein surface and its ability to self-assemble into colloidal membranes. Additionally, its single-stranded (ss) genome is commonly used as scaffold for DNA origami. Despite the manifold uses of M13, upstream production methods for phage and scaffold ssDNA are underexamined with respect to future industrial usage. Here, the high-cell-density phage production with Escherichia coli as host organism was studied in respect of medium composition, infection time, multiplicity of infection, and specific growth rate. The specific growth rate and the multiplicity of infection were identified as the crucial state variables that influence phage amplification rate on one hand and the concentration of produced ssDNA on the other hand. Using a growth rate of 0.15 h−1 and a multiplicity of infection of 0.05 pfu cfu−1 in the fed-batch production process, the concentration of pure isolated M13 ssDNA usable for scaffolded DNA origami could be enhanced by 54% to 590 mg L−1. Thus, our results help enabling M13 production for industrial uses in nanobiotechnology. Biotechnol. Bioeng. 2017;114: 777–784.' article_processing_charge: No article_type: original author: - first_name: Benjamin full_name: Kick, Benjamin last_name: Kick - first_name: Samantha full_name: Hensler, Samantha last_name: Hensler - first_name: Florian M full_name: Praetorius, Florian M id: dfec9381-4341-11ee-8fd8-faa02bba7d62 last_name: Praetorius - first_name: Hendrik full_name: Dietz, Hendrik last_name: Dietz - first_name: Dirk full_name: Weuster-Botz, Dirk last_name: Weuster-Botz citation: ama: Kick B, Hensler S, Praetorius FM, Dietz H, Weuster-Botz D. Specific growth rate and multiplicity of infection affect high-cell-density fermentation with bacteriophage M13 for ssDNA production. Biotechnology and Bioengineering. 2017;114(4):777-784. doi:10.1002/bit.26200 apa: Kick, B., Hensler, S., Praetorius, F. M., Dietz, H., & Weuster-Botz, D. (2017). Specific growth rate and multiplicity of infection affect high-cell-density fermentation with bacteriophage M13 for ssDNA production. Biotechnology and Bioengineering. Wiley. https://doi.org/10.1002/bit.26200 chicago: Kick, Benjamin, Samantha Hensler, Florian M Praetorius, Hendrik Dietz, and Dirk Weuster-Botz. “Specific Growth Rate and Multiplicity of Infection Affect High-Cell-Density Fermentation with Bacteriophage M13 for SsDNA Production.” Biotechnology and Bioengineering. Wiley, 2017. https://doi.org/10.1002/bit.26200. ieee: B. Kick, S. Hensler, F. M. Praetorius, H. Dietz, and D. Weuster-Botz, “Specific growth rate and multiplicity of infection affect high-cell-density fermentation with bacteriophage M13 for ssDNA production,” Biotechnology and Bioengineering, vol. 114, no. 4. Wiley, pp. 777–784, 2017. ista: Kick B, Hensler S, Praetorius FM, Dietz H, Weuster-Botz D. 2017. Specific growth rate and multiplicity of infection affect high-cell-density fermentation with bacteriophage M13 for ssDNA production. Biotechnology and Bioengineering. 114(4), 777–784. mla: Kick, Benjamin, et al. “Specific Growth Rate and Multiplicity of Infection Affect High-Cell-Density Fermentation with Bacteriophage M13 for SsDNA Production.” Biotechnology and Bioengineering, vol. 114, no. 4, Wiley, 2017, pp. 777–84, doi:10.1002/bit.26200. short: B. Kick, S. Hensler, F.M. Praetorius, H. Dietz, D. Weuster-Botz, Biotechnology and Bioengineering 114 (2017) 777–784. date_created: 2023-09-06T12:08:29Z date_published: 2017-04-01T00:00:00Z date_updated: 2023-11-07T12:36:20Z day: '01' doi: 10.1002/bit.26200 extern: '1' external_id: pmid: - '27748519' intvolume: ' 114' issue: '4' keyword: - Applied Microbiology and Biotechnology - Bioengineering - Biotechnology language: - iso: eng month: '04' oa_version: None page: 777-784 pmid: 1 publication: Biotechnology and Bioengineering publication_identifier: issn: - 0006-3592 publication_status: published publisher: Wiley quality_controlled: '1' scopus_import: '1' status: public title: Specific growth rate and multiplicity of infection affect high-cell-density fermentation with bacteriophage M13 for ssDNA production type: journal_article user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 114 year: '2017' ... --- _id: '15162' abstract: - lang: eng text: Cytological profiling (CP) is an unbiased image-based screening technique that uses automated microscopy and image analysis to profile compounds based on numerous quantifiable phenotypic features. We used CP to evaluate a library of nearly 500 compounds with documented mechanisms of action (MOAs) spanning a wide range of biological pathways. We developed informatics techniques for generating dosage-independent phenotypic “fingerprints” for each compound, and for quantifying the likelihood that a compound's CP fingerprint corresponds to its annotated MOA. We identified groups of features that distinguish classes with closely related phenotypes, such as microtubule poisons vs. HSP90 inhibitors, and DNA synthesis vs. proteasome inhibitors. We tested several cases in which cytological profiles indicated novel mechanisms, including a tyrphostin kinase inhibitor involved in mitochondrial uncoupling, novel microtubule poisons, and a nominal PPAR-gamma ligand that acts as a proteasome inhibitor, using independent biochemical assays to confirm the MOAs predicted by the CP signatures. We also applied maximal-information statistics to identify correlations between cytological features and kinase inhibitory activities by combining the CP fingerprints of 24 kinase inhibitors with published data on their specificities against a diverse panel of kinases. The resulting analysis suggests a strategy for probing the biological functions of specific kinases by compiling cytological data from inhibitors of varying specificities. article_number: '2604' article_processing_charge: No article_type: original author: - first_name: Marcos H. full_name: Woehrmann, Marcos H. last_name: Woehrmann - first_name: Walter M. full_name: Bray, Walter M. last_name: Bray - first_name: James K. full_name: Durbin, James K. last_name: Durbin - first_name: Sean C. full_name: Nisam, Sean C. last_name: Nisam - first_name: Alicia Kathleen full_name: Michael, Alicia Kathleen id: 6437c950-2a03-11ee-914d-d6476dd7b75c last_name: Michael - first_name: Emerson full_name: Glassey, Emerson last_name: Glassey - first_name: Joshua M. full_name: Stuart, Joshua M. last_name: Stuart - first_name: R. Scott full_name: Lokey, R. Scott last_name: Lokey citation: ama: Woehrmann MH, Bray WM, Durbin JK, et al. Large-scale cytological profiling for functional analysis of bioactive compounds. Molecular BioSystems. 2013;9(11). doi:10.1039/c3mb70245f apa: Woehrmann, M. H., Bray, W. M., Durbin, J. K., Nisam, S. C., Michael, A. K., Glassey, E., … Lokey, R. S. (2013). Large-scale cytological profiling for functional analysis of bioactive compounds. Molecular BioSystems. Royal Society of Chemistry. https://doi.org/10.1039/c3mb70245f chicago: Woehrmann, Marcos H., Walter M. Bray, James K. Durbin, Sean C. Nisam, Alicia K. Michael, Emerson Glassey, Joshua M. Stuart, and R. Scott Lokey. “Large-Scale Cytological Profiling for Functional Analysis of Bioactive Compounds.” Molecular BioSystems. Royal Society of Chemistry, 2013. https://doi.org/10.1039/c3mb70245f. ieee: M. H. Woehrmann et al., “Large-scale cytological profiling for functional analysis of bioactive compounds,” Molecular BioSystems, vol. 9, no. 11. Royal Society of Chemistry, 2013. ista: Woehrmann MH, Bray WM, Durbin JK, Nisam SC, Michael AK, Glassey E, Stuart JM, Lokey RS. 2013. Large-scale cytological profiling for functional analysis of bioactive compounds. Molecular BioSystems. 9(11), 2604. mla: Woehrmann, Marcos H., et al. “Large-Scale Cytological Profiling for Functional Analysis of Bioactive Compounds.” Molecular BioSystems, vol. 9, no. 11, 2604, Royal Society of Chemistry, 2013, doi:10.1039/c3mb70245f. short: M.H. Woehrmann, W.M. Bray, J.K. Durbin, S.C. Nisam, A.K. Michael, E. Glassey, J.M. Stuart, R.S. Lokey, Molecular BioSystems 9 (2013). date_created: 2024-03-21T07:58:57Z date_published: 2013-08-20T00:00:00Z date_updated: 2024-03-25T11:45:46Z day: '20' doi: 10.1039/c3mb70245f extern: '1' intvolume: ' 9' issue: '11' keyword: - Molecular Biology - Biotechnology language: - iso: eng month: '08' oa_version: None publication: Molecular BioSystems publication_identifier: eissn: - 1742-2051 issn: - 1742-206X publication_status: published publisher: Royal Society of Chemistry quality_controlled: '1' scopus_import: '1' status: public title: Large-scale cytological profiling for functional analysis of bioactive compounds type: journal_article user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 9 year: '2013' ... --- _id: '13408' abstract: - lang: eng text: Well-defined metallic nanobowls can be prepared by extending the concept of a protecting group to colloidal synthesis. Magnetic nanoparticles are employed as “protecting groups” during the galvanic replacement of silver with gold. The replacement reaction is accompanied by spontantous dissociation of the protecting groups, leaving behind metallic nanobowls. article_processing_charge: No article_type: original author: - first_name: Yonatan full_name: Ridelman, Yonatan last_name: Ridelman - first_name: Gurvinder full_name: Singh, Gurvinder last_name: Singh - first_name: Ronit full_name: Popovitz-Biro, Ronit last_name: Popovitz-Biro - first_name: Sharon G. full_name: Wolf, Sharon G. last_name: Wolf - first_name: Sanjib full_name: Das, Sanjib last_name: Das - first_name: Rafal full_name: Klajn, Rafal id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b last_name: Klajn citation: ama: Ridelman Y, Singh G, Popovitz-Biro R, Wolf SG, Das S, Klajn R. Metallic nanobowls by galvanic replacement reaction on heterodimeric nanoparticles. Small. 2012;8(5):654-660. doi:10.1002/smll.201101882 apa: Ridelman, Y., Singh, G., Popovitz-Biro, R., Wolf, S. G., Das, S., & Klajn, R. (2012). Metallic nanobowls by galvanic replacement reaction on heterodimeric nanoparticles. Small. Wiley. https://doi.org/10.1002/smll.201101882 chicago: Ridelman, Yonatan, Gurvinder Singh, Ronit Popovitz-Biro, Sharon G. Wolf, Sanjib Das, and Rafal Klajn. “Metallic Nanobowls by Galvanic Replacement Reaction on Heterodimeric Nanoparticles.” Small. Wiley, 2012. https://doi.org/10.1002/smll.201101882. ieee: Y. Ridelman, G. Singh, R. Popovitz-Biro, S. G. Wolf, S. Das, and R. Klajn, “Metallic nanobowls by galvanic replacement reaction on heterodimeric nanoparticles,” Small, vol. 8, no. 5. Wiley, pp. 654–660, 2012. ista: Ridelman Y, Singh G, Popovitz-Biro R, Wolf SG, Das S, Klajn R. 2012. Metallic nanobowls by galvanic replacement reaction on heterodimeric nanoparticles. Small. 8(5), 654–660. mla: Ridelman, Yonatan, et al. “Metallic Nanobowls by Galvanic Replacement Reaction on Heterodimeric Nanoparticles.” Small, vol. 8, no. 5, Wiley, 2012, pp. 654–60, doi:10.1002/smll.201101882. short: Y. Ridelman, G. Singh, R. Popovitz-Biro, S.G. Wolf, S. Das, R. Klajn, Small 8 (2012) 654–660. date_created: 2023-08-01T09:47:55Z date_published: 2012-03-12T00:00:00Z date_updated: 2023-08-08T07:55:10Z day: '12' doi: 10.1002/smll.201101882 extern: '1' external_id: pmid: - '22392681' intvolume: ' 8' issue: '5' keyword: - Biomaterials - Biotechnology - General Materials Science - General Chemistry language: - iso: eng month: '03' oa_version: None page: 654-660 pmid: 1 publication: Small publication_identifier: eissn: - 1613-6829 issn: - 1613-6810 publication_status: published publisher: Wiley quality_controlled: '1' scopus_import: '1' status: public title: Metallic nanobowls by galvanic replacement reaction on heterodimeric nanoparticles type: journal_article user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 8 year: '2012' ... --- _id: '13411' abstract: - lang: eng text: Photoresponsive gold nanoparticles dispersed in a solid/frozen matrix provide a basis for sensors that “remember” whether the sample has ever exceeded the melting temperature of the matrix. The operation of these sensors rests on the ability to photoinduce metastable electric dipoles on NP surfaces – upon melting, these dipoles drive NP aggregation, precipitation, and crosslinking. These events are manifested by a pronounced color change. article_processing_charge: No article_type: original author: - first_name: Rafal full_name: Klajn, Rafal id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b last_name: Klajn - first_name: Kevin P. full_name: Browne, Kevin P. last_name: Browne - first_name: Siowling full_name: Soh, Siowling last_name: Soh - first_name: Bartosz A. full_name: Grzybowski, Bartosz A. last_name: Grzybowski citation: ama: Klajn R, Browne KP, Soh S, Grzybowski BA. Nanoparticles that “remember” temperature. Small. 2010;6(13):1385-1387. doi:10.1002/smll.200902272 apa: Klajn, R., Browne, K. P., Soh, S., & Grzybowski, B. A. (2010). Nanoparticles that “remember” temperature. Small. Wiley. https://doi.org/10.1002/smll.200902272 chicago: Klajn, Rafal, Kevin P. Browne, Siowling Soh, and Bartosz A. Grzybowski. “Nanoparticles That ‘Remember’ Temperature.” Small. Wiley, 2010. https://doi.org/10.1002/smll.200902272. ieee: R. Klajn, K. P. Browne, S. Soh, and B. A. Grzybowski, “Nanoparticles that ‘remember’ temperature,” Small, vol. 6, no. 13. Wiley, pp. 1385–1387, 2010. ista: Klajn R, Browne KP, Soh S, Grzybowski BA. 2010. Nanoparticles that “remember” temperature. Small. 6(13), 1385–1387. mla: Klajn, Rafal, et al. “Nanoparticles That ‘Remember’ Temperature.” Small, vol. 6, no. 13, Wiley, 2010, pp. 1385–87, doi:10.1002/smll.200902272. short: R. Klajn, K.P. Browne, S. Soh, B.A. Grzybowski, Small 6 (2010) 1385–1387. date_created: 2023-08-01T09:48:38Z date_published: 2010-07-05T00:00:00Z date_updated: 2023-08-08T08:15:25Z day: '05' doi: 10.1002/smll.200902272 extern: '1' external_id: pmid: - '20521264' intvolume: ' 6' issue: '13' keyword: - Biomaterials - Biotechnology - General Materials Science - General Chemistry language: - iso: eng month: '07' oa_version: None page: 1385-1387 pmid: 1 publication: Small publication_identifier: eissn: - 1613-6829 issn: - 1613-6810 publication_status: published publisher: Wiley quality_controlled: '1' scopus_import: '1' status: public title: Nanoparticles that “remember” temperature type: journal_article user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 6 year: '2010' ... --- _id: '13414' abstract: - lang: eng text: Supraspherical aggregates of crosslinked metal nanoparticles are transformed into pancakes and nanorods by mechanical stresses and shears imparted by macroscopic objects (see image). The dimensions of both types of nanostructures can be controlled by the pressures applied. article_processing_charge: No article_type: original author: - first_name: Kevin P. full_name: Browne, Kevin P. last_name: Browne - first_name: Rafal full_name: Klajn, Rafal id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b last_name: Klajn - first_name: JulieAnn full_name: Villa, JulieAnn last_name: Villa - first_name: Bartosz A. full_name: Grzybowski, Bartosz A. last_name: Grzybowski citation: ama: Browne KP, Klajn R, Villa J, Grzybowski BA. Mechanofabrication of pancake and rodlike nanostructures from deformable nanoparticle aggregates. Small. 2009;5(23):2656-2658. doi:10.1002/smll.200900902 apa: Browne, K. P., Klajn, R., Villa, J., & Grzybowski, B. A. (2009). Mechanofabrication of pancake and rodlike nanostructures from deformable nanoparticle aggregates. Small. Wiley. https://doi.org/10.1002/smll.200900902 chicago: Browne, Kevin P., Rafal Klajn, JulieAnn Villa, and Bartosz A. Grzybowski. “Mechanofabrication of Pancake and Rodlike Nanostructures from Deformable Nanoparticle Aggregates.” Small. Wiley, 2009. https://doi.org/10.1002/smll.200900902. ieee: K. P. Browne, R. Klajn, J. Villa, and B. A. Grzybowski, “Mechanofabrication of pancake and rodlike nanostructures from deformable nanoparticle aggregates,” Small, vol. 5, no. 23. Wiley, pp. 2656–2658, 2009. ista: Browne KP, Klajn R, Villa J, Grzybowski BA. 2009. Mechanofabrication of pancake and rodlike nanostructures from deformable nanoparticle aggregates. Small. 5(23), 2656–2658. mla: Browne, Kevin P., et al. “Mechanofabrication of Pancake and Rodlike Nanostructures from Deformable Nanoparticle Aggregates.” Small, vol. 5, no. 23, Wiley, 2009, pp. 2656–58, doi:10.1002/smll.200900902. short: K.P. Browne, R. Klajn, J. Villa, B.A. Grzybowski, Small 5 (2009) 2656–2658. date_created: 2023-08-01T09:50:12Z date_published: 2009-12-01T00:00:00Z date_updated: 2023-08-08T08:49:22Z day: '01' doi: 10.1002/smll.200900902 extern: '1' external_id: pmid: - '19771567' intvolume: ' 5' issue: '23' keyword: - Biomaterials - Biotechnology - General Materials Science - General Chemistry language: - iso: eng month: '12' oa_version: None page: 2656-2658 pmid: 1 publication: Small publication_identifier: eissn: - 1613-6829 issn: - 1613-6810 publication_status: published publisher: Wiley quality_controlled: '1' scopus_import: '1' status: public title: Mechanofabrication of pancake and rodlike nanostructures from deformable nanoparticle aggregates type: journal_article user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 5 year: '2009' ... --- _id: '13422' abstract: - lang: eng text: 'Make like a leaf: The synthesis and characterization of a family of “flowerlike” Au/Fe3O4 nanoparticles is described, whereby Fe3O4 “leaves” adhere to a gold core (see image). The size and numbers of iron oxide domains can be adjusted flexibly by changing the proportion of the starting materials and the reaction time.' article_processing_charge: No article_type: original author: - first_name: Yanhu full_name: Wei, Yanhu last_name: Wei - first_name: Rafal full_name: Klajn, Rafal id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b last_name: Klajn - first_name: Anatoliy O. full_name: Pinchuk, Anatoliy O. last_name: Pinchuk - first_name: Bartosz A. full_name: Grzybowski, Bartosz A. last_name: Grzybowski citation: ama: Wei Y, Klajn R, Pinchuk AO, Grzybowski BA. Synthesis, shape control, and optical properties of hybrid Au/Fe3O4 “nanoflowers.” Small. 2008;4(10):1635-1639. doi:10.1002/smll.200800511 apa: Wei, Y., Klajn, R., Pinchuk, A. O., & Grzybowski, B. A. (2008). Synthesis, shape control, and optical properties of hybrid Au/Fe3O4 “nanoflowers.” Small. Wiley. https://doi.org/10.1002/smll.200800511 chicago: Wei, Yanhu, Rafal Klajn, Anatoliy O. Pinchuk, and Bartosz A. Grzybowski. “Synthesis, Shape Control, and Optical Properties of Hybrid Au/Fe3O4 ‘Nanoflowers.’” Small. Wiley, 2008. https://doi.org/10.1002/smll.200800511. ieee: Y. Wei, R. Klajn, A. O. Pinchuk, and B. A. Grzybowski, “Synthesis, shape control, and optical properties of hybrid Au/Fe3O4 ‘nanoflowers,’” Small, vol. 4, no. 10. Wiley, pp. 1635–1639, 2008. ista: Wei Y, Klajn R, Pinchuk AO, Grzybowski BA. 2008. Synthesis, shape control, and optical properties of hybrid Au/Fe3O4 “nanoflowers”. Small. 4(10), 1635–1639. mla: Wei, Yanhu, et al. “Synthesis, Shape Control, and Optical Properties of Hybrid Au/Fe3O4 ‘Nanoflowers.’” Small, vol. 4, no. 10, Wiley, 2008, pp. 1635–39, doi:10.1002/smll.200800511. short: Y. Wei, R. Klajn, A.O. Pinchuk, B.A. Grzybowski, Small 4 (2008) 1635–1639. date_created: 2023-08-01T10:30:42Z date_published: 2008-10-09T00:00:00Z date_updated: 2023-08-08T11:14:50Z day: '09' doi: 10.1002/smll.200800511 extern: '1' external_id: pmid: - '18636405' intvolume: ' 4' issue: '10' keyword: - Biomaterials - Biotechnology - General Materials Science - General Chemistry language: - iso: eng month: '10' oa_version: None page: 1635-1639 pmid: 1 publication: Small publication_identifier: eissn: - 1613-6829 issn: - 1613-6810 publication_status: published publisher: Wiley quality_controlled: '1' scopus_import: '1' status: public title: Synthesis, shape control, and optical properties of hybrid Au/Fe3O4 “nanoflowers” type: journal_article user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 4 year: '2008' ...