TY - JOUR A1 - Aichert, Ingrid A1 - Staiger, Anja A1 - Schulte-Mäter, Anne A1 - Becker-Redding, Ulrike A1 - Stahn, Corinna A1 - Peschke, Claudia A1 - Heide, Judith A1 - Ott, Susan A1 - Herrmann, Heike A1 - Völsch, Juliane A1 - Mayer, Jörg A1 - Rohnke, Lucie A1 - Frank, Ulrike A1 - Stadie, Nicole A1 - Jentsch, Nadine A1 - Blech, Anke A1 - Kurtenbach, Stephanie A1 - Thieke, Johanna A1 - Schröder, Astrid A1 - Stahn, Corinna A1 - Hörnig, Robin A1 - Burchert, Frank A1 - De Bleser, Ria A1 - Heister, Julian A1 - Bartels, Luise A1 - Würzner, Kay-Michael A1 - Böhme, Romy A1 - Burmester, Juliane A1 - Krajewski, Melanie A1 - Nager, Wido A1 - Jungehülsing, Gerhard Jan A1 - Wartenburger, Isabell A1 - Jöbges, Michael A1 - Schwilling, Eleonore A1 - Lidzba, Karen A1 - Winkler, Susanne A1 - Konietzko, Andreas A1 - Krägeloh-Mann, Ingeborg A1 - Rilling, Eva A1 - Wilken, Rainer A1 - Wismann, Kathrin A1 - Glandorf, Birte A1 - Hoffmann, Hannah A1 - Hinnenkamp, Christiane A1 - Rohlmann, Insa A1 - Ludewigt, Jacqueline A1 - Bittner, Christian A1 - Orlov, Tatjana A1 - Claus, Katrin A1 - Ehemann, Christine A1 - Winnecken, Andreas A1 - Hummel, Katja A1 - Breitenstein, Sarah ED - Wahl, Michael ED - Stahn, Corinna ED - Hanne, Sandra ED - Fritzsche, Tom T1 - Spektrum Patholinguistik = Schwerpunktthema: Von der Programmierung zur Artikulation : Sprechapraxie bei Kindern und Erwachsenen N2 - Das 3. Herbsttreffen Patholinguistik fand am 21. November 2009 an der Universität Potsdam statt. Der vorliegende Tagungsband enthält die drei Hauptvorträge zum Schwerpunktthema „Von der Programmierung zu Artikulation: Sprechapraxie bei Kindern und Erwachsenen“. Darüber hinaus enthält der Band die Beiträge aus dem Spektrum Patholinguistik, sowie die Abstracts der Posterpräsentationen. N2 - The 3rd Herbsttreffen Patholinguistik was held on November 21st, 2009 at the University of Potsdam. These proceedings contain the three main lectures of the central topic „From programming to articulation: Apraxia of speech of children and adults “. Additionally this volume contains the contributions of Spektrum Patholinguistik, as well as the abstracts of the poster presentations. T3 - Spektrum Patholinguistik - 3 KW - Patholinguistik KW - Sprechapraxie KW - Sprachtherapie KW - patholinguistics KW - apraxia of speech KW - speech and language therapy Y1 - 2010 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus-45470 SN - 978-3-86956-079-3 SN - 1869-3822 SN - 1866-9433 IS - 3 PB - Universitätsverlag Potsdam CY - Potsdam ER - TY - THES A1 - Breitenstein, Michael T1 - Ortsaufgelöster Aufbau von DNA-Nanostrukturen auf Glasoberflächen T1 - Assembly of DNA nanostructures on glass surfaces N2 - Im Fokus dieser Arbeit stand der Aufbau einer auf DNA basierenden Nanostruktur. Der universelle Vier-Buchstaben-Code der DNA ermöglicht es, Bindungen auf molekularer Ebene zu adressieren. Die chemischen und physikalischen Eigenschaften der DNA prädestinieren dieses Makromolekül für den Einsatz und die Verwendung als Konstruktionselement zum Aufbau von Nanostrukturen. Das Ziel dieser Arbeit war das Aufspannen eines DNA-Stranges zwischen zwei Fixpunkten. Hierfür war es notwendig, eine Methode zu entwickeln, welche es ermöglicht, Funktionsmoleküle als Ankerelemente ortsaufgelöst auf eine Oberfläche zu deponieren. Das Deponieren dieser Moleküle sollte dabei im unteren Mikrometermaßstab erfolgen, um den Abmaßen der DNA und der angestrebten Nanostruktur gerecht zu werden. Das eigens für diese Aufgabe entwickelte Verfahren zum ortsaufgelösten Deponieren von Funktionsmolekülen nutzt das Bindungspaar Biotin-Neutravidin. Mit Hilfe eines Rasterkraftmikroskops (AFM) wurde eine zu einem „Stift“ umfunktionierte Rasterkraftmikroskopspitze so mit der zu deponierenden „Tinte“ beladen, dass das Absetzen von Neutravidin im unteren Mikrometermaßstab möglich war. Dieses Neutravidinmolekül übernahm die Funktion als Bindeglied zwischen der biotinylierten Glasoberfläche und dem eigentlichen Adressmolekül. Das somit generierte Neutravidin-Feld konnte dann mit einem biotinylierten Adressmolekül durch Inkubation funktionalisiert werden. Namensgebend für dieses Verfahren war die Möglichkeit, Neutravidin mehrmals zu deponieren und zu adressieren. Somit ließ sich sequenziell ein Mehrkomponenten-Feld aufbauen. Die Einschränkung, mit einem AFM nur eine Substanz deponieren zu können, wurde so umgangen. Ferner mußten Ankerelemente geschaffen werden, um die DNA an definierten Punkten immobilisieren zu können. Die Bearbeitung der DNA erfolgte mit molekularbiologischen Methoden und zielte darauf ab, einen DNA-Strang zu generieren, welcher an seinen beiden Enden komplementäre Adressequenzen enthält, um gezielt mit den oberflächenständigen Ankerelementen binden zu können. Entsprechend der Geometrie der mit dem AFM erzeugten Fixpunkte und den oligonukleotidvermittelten Adressen kommt es zur Ausbildung einer definierten DNA-Struktur. Mit Hilfe von fluoreszenzmikroskopischen Methoden wurde die aufgebaute DNA-Nanostruktur nachgewiesen. Der Nachweis der nanoskaligen Interaktion von DNA-bindenden Molekülen mit der generierten DNA-Struktur wurde durch die Bindung von PNA (peptide nucleic acid) an den DNA-Doppelstrang erbracht. Diese PNA-Bindung stellt ihrerseits ein funktionales Strukturelement im Nanometermaßstab dar und wird als Nanostrukturbaustein verstanden. N2 - The main aim of this work was the development of a DNA-based nanostructure. The universal four-letter code of DNA allows addressing bonds at the molecular level. The chemical and physical property of DNA makes this macromolecule an ideal candidate as a construction element for nanostructures. The aim of this work was to span a DNA strand between two fixed points. For this purpose it was necessary to develop a method which makes it possible to deposit functional molecules as anchoring elements with highly spatial resolution on a surface. These molecules should be immobilized on the lower micrometer scale to meet the requirements of the desired nanostructure. The method that has been developed for this task, which enables to deposit functional molecules, uses the binding pair biotin-neutravidin. Using the tip of an atomic force microscope (AFM), which can be uses like a pen, it was possible to deposit neutravidin on the lower micrometer scale. This neutravidin molecule is the linking element between the biotinylated glass surface and the actual address molecule. The thus generated neutravidin field could then be functionalized with a biotinylated molecule by incubation. The method has been published as sequential spotting method because it enables a sequential functionalization of neutravidin after it has been deposited. It was so possible to build up a multi-component array. The limitation of being able to deposit only one single substance with an AFM has been circumvented. It also was necessary to create anchor elements in order to immobilize the DNA at defined positions. The processing of the DNA was carried out using molecular biological methods and aimed at generating a DNA strand, which at both ends has a complementary sequence for binding to the surface bound anchor elements. The defined structure is a result of the geometry of the fixed points, generated by the AFM. Using fluorescence microscopy, the constructed DNA nanostructure was detected. The proof of the interaction of DNA-binding molecules with the DNA structure was carried out by the binding of PNA (peptide nucleic acid), which is capable of binding to double stranded DNA. The PNA and its DNA-interaction is a functional building block in the nanometer scale and can be regarded as a promising nanostructure. KW - Nanostruktur KW - DNA KW - Rasterkraftmikroskop KW - Fluoreszenzmikroskopie KW - Oberflächenfunktionalisierung KW - nanostructure KW - DNA KW - atomic force microscope KW - fluorescence microscopy KW - surface chemistry Y1 - 2012 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus-61857 ER - TY - JOUR A1 - Schröder, Astrid A1 - Grimm, Angela A1 - Schulz, Petra A1 - Heide, Judith A1 - Frank, Ulrike A1 - Wahl, Michael A1 - Lampe, Leonie A1 - Fieder, Nora A1 - Krajenbrink, Trudy A1 - Nickels, Lyndsey A1 - Bykova, Ksenia A1 - Wilzek, Alexa A1 - van den Engl-Hoek, Lenie A1 - Huckabee, Maggie-Lee A1 - Balzer, Julia A1 - Ebert, Susanne A1 - Kaps, Hella A1 - Matteschk, Maria A1 - Tzschöckel, Katharina Andrea A1 - Dressel, Katharina A1 - Kröger, Bernd J. A1 - Diwoky, Laura Cassandra A1 - Breitenstein, Sarah A1 - Bruno, Giulia A1 - Lassotta, Romy A1 - Adani, Flavia A1 - Ferchland, Lisa A1 - Baatz, Charlotte A1 - Netzebandt, Jonka A1 - Heyde, Cornelia J. A1 - Cleland, Joanne A1 - Scobbie, James M. A1 - Roxburgh, Zoe A1 - Schmidt, Jessica ED - Adelt, Anne ED - Yetim, Özlem ED - Otto, Constanze ED - Fritzsche, Tom T1 - Spektrum Patholinguistik Band 10. Schwerpunktthema: Panorama Patholinguistik: Sprachwissenschaft trifft Sprachtherapie N2 - Das 10. Herbsttreffen Patholinguistik mit dem Schwerpunktthema »Panorama Patholinguistik: Sprachwissenschaft trifft Sprachtherapie« fand am 19.11.2016 in Potsdam statt. Das Herbsttreffen wird seit 2007 jährlich vom Verband für Patholinguistik e.V. (vpl) durchgeführt. Der vorliegende Tagungsband beinhaltet die vier Hauptvorträge zum Schwerpunktthema sowie Beiträge zu den Kurzvorträgen »Patholinguistik im Fokus« und der Posterpräsentationen zu weiteren Themen aus der sprachtherapeutischen Forschung und Praxis. N2 - The Tenth Autumn Meeting Patholinguistics (Herbsttreffen Patholinguistik) with its main topic »Panorama Patholinguistics: Linguistics meets speech/language therapy« took place in Potsdam on November 19 2016. This annual meeting has been organised since 2007 by the Association for Patholinguistics (Verband für Patholinguistik e.V./vpl). The present proceedings contain the four keynote talks on the main topic as well as contributions from the short talks in the section »Patholinguistics in Focus« and from the poster session covering a broad range of areas in speech/language therapy research and practice. T3 - Spektrum Patholinguistik - 10 KW - Patholinguistik KW - Sprachtherapie KW - Spracherwerb KW - Aphasie KW - Schluckstörungen KW - Lese-Rechtschreibschwierigkeiten KW - patholinguistics KW - speech/language therapy KW - language acquisition KW - ahasia KW - dysphagia KW - dyslexia Y1 - 2017 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-397019 SN - 978-3-86956-404-3 SN - 1866-9085 SN - 1866-9433 IS - 10 PB - Universitätsverlag Potsdam CY - Potsdam ER - TY - JOUR A1 - Breitenstein, Michael A1 - Nielsen, Peter E. A1 - Hölzel, Ralph A1 - Bier, Frank Fabian T1 - DNA-nanostructure-assembly by sequential spotting JF - Journal of nanobiotechnology N2 - Background: The ability to create nanostructures with biomolecules is one of the key elements in nanobiotechnology. One of the problems is the expensive and mostly custom made equipment which is needed for their development. We intended to reduce material costs and aimed at miniaturization of the necessary tools that are essential for nanofabrication. Thus we combined the capabilities of molecular ink lithography with DNA-self-assembling capabilities to arrange DNA in an independent array which allows addressing molecules in nanoscale dimensions. Results: For the construction of DNA based nanostructures a method is presented that allows an arrangement of DNA strands in such a way that they can form a grid that only depends on the spotted pattern of the anchor molecules. An atomic force microscope (AFM) has been used for molecular ink lithography to generate small spots. The sequential spotting process allows the immobilization of several different functional biomolecules with a single AFM-tip. This grid which delivers specific addresses for the prepared DNA-strand serves as a two-dimensional anchor to arrange the sequence according to the pattern. Once the DNA-nanoarray has been formed, it can be functionalized by PNA (peptide nucleic acid) to incorporate advanced structures. Conclusions: The production of DNA-nanoarrays is a promising task for nanobiotechnology. The described method allows convenient and low cost preparation of nanoarrays. PNA can be used for complex functionalization purposes as well as a structural element. Y1 - 2011 U6 - https://doi.org/10.1186/1477-3155-9-54 SN - 1477-3155 VL - 9 IS - 11 PB - BioMed Central CY - London ER - TY - GEN A1 - Breitenstein, Michael A1 - Nielsen, Peter E. A1 - Hölzel, Ralph A1 - Bier, Frank Fabian T1 - DNA-nanostructure-assembly by sequential spotting T2 - Postprints der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe N2 - Background: The ability to create nanostructures with biomolecules is one of the key elements in nanobiotechnology. One of the problems is the expensive and mostly custom made equipment which is needed for their development. We intended to reduce material costs and aimed at miniaturization of the necessary tools that are essential for nanofabrication. Thus we combined the capabilities of molecular ink lithography with DNA-self-assembling capabilities to arrange DNA in an independent array which allows addressing molecules in nanoscale dimensions. Results: For the construction of DNA based nanostructures a method is presented that allows an arrangement of DNA strands in such a way that they can form a grid that only depends on the spotted pattern of the anchor molecules. An atomic force microscope (AFM) has been used for molecular ink lithography to generate small spots. The sequential spotting process allows the immobilization of several different functional biomolecules with a single AFM-tip. This grid which delivers specific addresses for the prepared DNA-strand serves as a two-dimensional anchor to arrange the sequence according to the pattern. Once the DNA-nanoarray has been formed, it can be functionalized by PNA (peptide nucleic acid) to incorporate advanced structures. Conclusions: The production of DNA-nanoarrays is a promising task for nanobiotechnology. The described method allows convenient and low cost preparation of nanoarrays. PNA can be used for complex functionalization purposes as well as a structural element. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 1027 KW - atomic force microscope KW - peptide nucleic acid KW - persistence length KW - adapter oligonucleotide KW - high fluorescence signal Y1 - 2020 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-431108 SN - 1866-8372 IS - 1027 ER - TY - GEN A1 - Breitenstein, Michael A1 - Hölzel, Ralph A1 - Bier, Frank Fabian T1 - Immobilization of different biomolecules by atomic force microscopy T2 - Postprints der Universität Potsdam : Mathematisch Naturwissenschaftliche Reihe N2 - Background Micrometer resolution placement and immobilization of probe molecules is an important step in the preparation of biochips and a wide range of lab-on-chip systems. Most known methods for such a deposition of several different substances are costly and only suitable for a limited number of probes. In this article we present a flexible procedure for simultaneous spatially controlled immobilization of functional biomolecules by molecular ink lithography. Results For the bottom-up fabrication of surface bound nanostructures a universal method is presented that allows the immobilization of different types of biomolecules with micrometer resolution. A supporting surface is biotinylated and streptavidin molecules are deposited with an AFM (atomic force microscope) tip at distinct positions. Subsequent incubation with a biotinylated molecule species leads to binding only at these positions. After washing streptavidin is deposited a second time with the same AFM tip and then a second biotinylated molecule species is coupled by incubation. This procedure can be repeated several times. Here we show how to immobilize different types of biomolecules in an arbitrary arrangement whereas most common methods can deposit only one type of molecules. The presented method works on transparent as well as on opaque substrates. The spatial resolution is better than 400 nm and is limited only by the AFM's positional accuracy after repeated z-cycles since all steps are performed in situ without moving the supporting surface. The principle is demonstrated by hybridization to different immobilized DNA oligomers and was validated by fluorescence microscopy. Conclusions The immobilization of different types of biomolecules in high-density microarrays is a challenging task for biotechnology. The method presented here not only allows for the deposition of DNA at submicrometer resolution but also for proteins and other molecules of biological relevance that can be coupled to biotin. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 872 KW - Atomic Force Microscope KW - Immobilization KW - Cross Contamination KW - Roth GmbH KW - Microcontact Printing Y1 - 2020 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-435075 SN - 1866-8372 IS - 872 ER - TY - JOUR A1 - Aktas, Maren A1 - Succow, Juliane A1 - Giel, Barbara A1 - Dressel, Katharina A1 - Lange, Inga A1 - Hanne, Sandra A1 - Burchert, Frank A1 - Vasishth, Shravan A1 - Schwytay, Jeannine A1 - Breitenstein, Sarah A1 - Fleischhauer, Elisabeth A1 - Baumann, Jeannine A1 - Preisinger, Irmhild A1 - Siegmüller, Julia A1 - Kuschmann, Anja A1 - Ebert, Susanne A1 - Lowit, Anja A1 - Rath, Elisa A1 - Heide, Judith A1 - Lorenz, Antje A1 - Wartenburger, Isabell A1 - Hippeli, Carolin A1 - Rausch, Monika A1 - Würzner, Kay-Michael A1 - Schroeder, Sascha A1 - Czapka, Sophia A1 - Klassert, Annegret A1 - Reuters, Sabine A1 - Frank, Ulrike A1 - Frank, Katrin A1 - Zimmermann, Heinrich A1 - Peiffers, Sabine A1 - Thonicke, Mady ED - Adelt, Anne ED - Otto, Constanze ED - Fritzsche, Tom ED - Magister, Caroline T1 - Spektrum Patholinguistik = Schwerpunktthema: Besonders behandeln? : Sprachtherapie im Rahmen primärer Störungsbilder N2 - Das 8. Herbsttreffen Patholinguistik mit dem Schwerpunktthema "Besonders behandeln? Sprachtherapie im Rahmen primärer Störungsbilder" fand am 15.11.2014 in Potsdam statt. Das Herbsttreffen wird seit 2007 jährlich vom Verband für Patholinguistik e.V. (vpl) durchgeführt. Der vorliegende Tagungsband beinhaltet die vier Hauptvorträge zum Schwerpunktthema, die vier Kurzvorträge aus dem Spektrum Patholinguisitk sowie die Beiträge der Posterpräsentationen zu weiteren Themen aus der sprachtherapeutischen Forschung und Praxis. N2 - The Eighth Autumn Meeting Patholinguistics ('Herbsttreffen Patholinguistik') with its main topic "Special treatment? Language therapy in the context of primary disorders" took place in Potsdam on November 15 2014. This annual meeting has been organized since 2007 by the Association for Patholinguistics (Verband für Patholinguistik e.V./vpl). The present proceedings contain the four keynote talks on the main topic, the four short talks from the series 'Spectrum Patholinguistics', as well as the contributions of the poster session from all areas of speech/language therapy research and practice. T3 - Spektrum Patholinguistik - 8 KW - Patholinguistik KW - Sprachtherapie KW - geistige Behinderung KW - primär progessive Aphasie KW - patholinguistics KW - speech therapy KW - mental deficiency KW - primary progessive aphasia Y1 - 2015 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-77147 SN - 978-3-86956-335-0 SN - 1869-3822 SN - 1866-9433 IS - 8 PB - Universitätsverlag Potsdam CY - Potsdam ER -