24 research outputs found

    Development and Experimental Assessment of a Model for the Material Deposition by Laser-Induced Forward Transfer

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    The potential to deposit minute amounts of material from a donor to an acceptor substrate at precise locations makes laser-induced forward transfer (LIFT) a frequently used tool within different research fields, such as materials science and biotechnology. While many different types of LIFT exist, each specialized LIFT application is based on a different underlying transfer mechanism, which affects the to-be-transferred materials in different ways. Thus, a characterization of these mechanisms is necessary to understand their limitations. The most common investigative methods are high-speed imaging and numerical modeling. However, neither of these can, to date, quantify the material deposition. Here, analytical solutions are derived for the contact-based material deposition by LIFT, which are based on a previously observed equilibrium state. Moreover, an analytical solution for the previously unrecognized ejection-based material deposition is proposed, which is detectable by introducing a distance between the donor and acceptor substrates. This secondary mechanism is particularly relevant in large scale production, since each deposition from a donor substrate potentially induces a local distance between the donor and acceptor substrates.Peer Reviewe

    Development and Experimental Assessment of a Model for the Material Deposition by Laser-Induced Forward Transfer

    Get PDF
    The potential to deposit minute amounts of material from a donor to an acceptor substrate at precise locations makes laser-induced forward transfer (LIFT) a frequently used tool within different research fields, such as materials science and biotechnology. While many different types of LIFT exist, each specialized LIFT application is based on a different underlying transfer mechanism, which affects the to-be-transferred materials in different ways. Thus, a characterization of these mechanisms is necessary to understand their limitations. The most common investigative methods are high-speed imaging and numerical modeling. However, neither of these can, to date, quantify the material deposition. Here, analytical solutions are derived for the contact-based material deposition by LIFT, which are based on a previously observed equilibrium state. Moreover, an analytical solution for the previously unrecognized ejection-based material deposition is proposed, which is detectable by introducing a distance between the donor and acceptor substrates. This secondary mechanism is particularly relevant in large scale production, since each deposition from a donor substrate potentially induces a local distance between the donor and acceptor substrates

    Development and Experimental Assessment of a Model for the Material Deposition by Laser-Induced Forward Transfer

    Get PDF
    The potential to deposit minute amounts of material from a donor to an acceptor substrate at precise locations makes laser-induced forward transfer (LIFT) a frequently used tool within different research fields, such as materials science and biotechnology. While many different types of LIFT exist, each specialized LIFT application is based on a different underlying transfer mechanism, which affects the to-be-transferred materials in different ways. Thus, a characterization of these mechanisms is necessary to understand their limitations. The most common investigative methods are high-speed imaging and numerical modeling. However, neither of these can, to date, quantify the material deposition. Here, analytical solutions are derived for the contact-based material deposition by LIFT, which are based on a previously observed equilibrium state. Moreover, an analytical solution for the previously unrecognized ejection-based material deposition is proposed, which is detectable by introducing a distance between the donor and acceptor substrates. This secondary mechanism is particularly relevant in large scale production, since each deposition from a donor substrate potentially induces a local distance between the donor and acceptor substrates.BMBF, 13XP5050A, Erforschung einer neuen Methode für die Herstellung von hochdichten Molekülbibliotheken (cLIFT

    Automated Laser‐Transfer Synthesis of High‐Density Microarrays for Infectious Disease Screening

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    Laser-induced forward transfer (LIFT) is a rapid laser-patterning technique for high-throughput combinatorial synthesis directly on glass slides. A lack of automation and precision limits LIFT applications to simple proof-of-concept syntheses of fewer than 100 compounds. Here, an automated synthesis instrument is reported that combines laser transfer and robotics for parallel synthesis in a microarray format with up to 10 000 individual reactions cm−2. An optimized pipeline for amide bond formation is the basis for preparing complex peptide microarrays with thousands of different sequences in high yield with high reproducibility. The resulting peptide arrays are of higher quality than commercial peptide arrays. More than 4800 15-residue peptides resembling the entire Ebola virus proteome on a microarray are synthesized to study the antibody response of an Ebola virus infection survivor. Known and unknown epitopes that serve now as a basis for Ebola diagnostic development are identified. The versatility and precision of the synthesizer is demonstrated by in situ synthesis of fluorescent molecules via Schiff base reaction and multi-step patterning of precisely definable amounts of fluorophores. This automated laser transfer synthesis approach opens new avenues for high-throughput chemical synthesis and biological screening

    Search for dark matter produced in association with bottom or top quarks in √s = 13 TeV pp collisions with the ATLAS detector

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    A search for weakly interacting massive particle dark matter produced in association with bottom or top quarks is presented. Final states containing third-generation quarks and miss- ing transverse momentum are considered. The analysis uses 36.1 fb−1 of proton–proton collision data recorded by the ATLAS experiment at √s = 13 TeV in 2015 and 2016. No significant excess of events above the estimated backgrounds is observed. The results are in- terpreted in the framework of simplified models of spin-0 dark-matter mediators. For colour- neutral spin-0 mediators produced in association with top quarks and decaying into a pair of dark-matter particles, mediator masses below 50 GeV are excluded assuming a dark-matter candidate mass of 1 GeV and unitary couplings. For scalar and pseudoscalar mediators produced in association with bottom quarks, the search sets limits on the production cross- section of 300 times the predicted rate for mediators with masses between 10 and 50 GeV and assuming a dark-matter mass of 1 GeV and unitary coupling. Constraints on colour- charged scalar simplified models are also presented. Assuming a dark-matter particle mass of 35 GeV, mediator particles with mass below 1.1 TeV are excluded for couplings yielding a dark-matter relic density consistent with measurements

    Measurement of the W boson polarisation in ttˉt\bar{t} events from pp collisions at s\sqrt{s} = 8 TeV in the lepton + jets channel with ATLAS

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    Measurement of jet fragmentation in Pb+Pb and pppp collisions at sNN=2.76\sqrt{{s_\mathrm{NN}}} = 2.76 TeV with the ATLAS detector at the LHC

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    Search for new phenomena in events containing a same-flavour opposite-sign dilepton pair, jets, and large missing transverse momentum in s=\sqrt{s}= 13 pppp collisions with the ATLAS detector

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    Automated Laser-Transfer Synthesis of High-Density Microarrays for Infectious Disease Screening

    Get PDF
    Laser-induced forward transfer (LIFT) is a rapid laser-patterning technique for high-throughput combinatorial synthesis directly on glass slides. A lack of automation and precision limits LIFT applications to simple proof-of-concept syntheses of fewer than 100 compounds. Here, an automated synthesis instrument is reported that combines laser transfer and robotics for parallel synthesis in a microarray format with up to 10 000 individual reactions cm−2. An optimized pipeline for amide bond formation is the basis for preparing complex peptide microarrays with thousands of different sequences in high yield with high reproducibility. The resulting peptide arrays are of higher quality than commercial peptide arrays. More than 4800 15-residue peptides resembling the entire Ebola virus proteome on a microarray are synthesized to study the antibody response of an Ebola virus infection survivor. Known and unknown epitopes that serve now as a basis for Ebola diagnostic development are identified. The versatility and precision of the synthesizer is demonstrated by in situ synthesis of fluorescent molecules via Schiff base reaction and multi-step patterning of precisely definable amounts of fluorophores. This automated laser transfer synthesis approach opens new avenues for high-throughput chemical synthesis and biological screening

    On‐Chip Neo‐Glycopeptide Synthesis for Multivalent Glycan Presentation

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    Single glycan–protein interactions are often weak, such that glycan binding partners commonly utilize multiple, spatially defined binding sites to enhance binding avidity and specificity. Current array technologies usually neglect defined multivalent display. Laser‐based array synthesis technology allows for flexible and rapid on‐surface synthesis of different peptides. By combining this technique with click chemistry, neo‐glycopeptides were produced directly on a functionalized glass slide in the microarray format. Density and spatial distribution of carbohydrates can be tuned, resulting in well‐defined glycan structures for multivalent display. The two lectins concanavalin A and langerin were probed with different glycans on multivalent scaffolds, revealing strong spacing‐, density‐, and ligand‐dependent binding. In addition, we could also measure the surface dissociation constant. This approach allows for a rapid generation, screening, and optimization of a multitude of multivalent scaffolds for glycan binding
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