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    • 2. 发明申请
    • METHOD OF PRODUCING THREE-DIMENSIONAL STRUCTURES USING MOTOR PROTEINS
    • 使用电机蛋白质生产三维结构的方法
    • WO2004096831A3
    • 2005-03-03
    • PCT/EP2004004630
    • 2004-04-30
    • MAX PLANCK GESELLSCHAFTUNIV DRESDEN TECHDIEZ STEFANREUTHER CORDULAHOWARD JONATHONSEIDEL RALFMERTIG MICHAELPOMPE WOLFGANGBERGMANN MAX
    • DIEZ STEFANREUTHER CORDULAHOWARD JONATHONSEIDEL RALFMERTIG MICHAELPOMPE WOLFGANGBERGMANN MAX
    • C07K17/02C07K17/00
    • B82Y30/00C07K17/02
    • The present invention relates to a method of producing a three-dimensional structure of a nanornaterial on a surface comprising the step of (a) contacting said polymer material affixed to (aa) biological filaments with biologically active motor proteins carried by said surface; or (ab) biologically active motor proteins with biological filaments carried by said surface in the presence of an energy source in a buffer having a pH value of 5 to 9 and containing monovalent or divalent cations. It is preferred that said nanomaterial is carbon nanotubes or DNA and that said biological filaments are actin filaments or microtubules. It is further preferred that said motor proteins are kinesin or myosin molecules. Also preferred is that said DNA carries metal ions. In particular, the metal ions can be attached to the DNA before or after structure formation. The invention additionally relates to a three-dimensional structure of nanornaterial obtainable by the method of the invention. Said three-dimensional structure preferably is a nanocircuit of metallized DNA.
    • 本发明涉及一种在表面上制造纳米材料的三维结构的方法,其包括以下步骤:(a)将附着于(aa)生物细丝的所述聚合物材料与由所述表面携带的生物活性运动蛋白接触; 或(ab)生物活性的运动蛋白,其具有在能量源存在下由所述表面承载的具有pH值为5至9并含有一价或二价阳离子的缓冲液中的生物细丝。 所述纳米材料优选为碳纳米管或DNA,所述生物细丝为肌动蛋白丝或微管。 更优选所述运动蛋白是驱动蛋白或肌球蛋白分子。 所述DNA还优选携带金属离子。 特别地,金属离子可以在结构形成之前或之后连接到DNA。 本发明还涉及通过本发明的方法获得的纳米材料的三维结构。 所述三维结构优选为金属化DNA的纳米电路。
    • 10. 发明专利
    • Detection of microorganisms and/or their activity by biosensors, by immobilizing ligands for binding a receptor at a substrate surface or immobilizing the receptor for the ligands at the surface in chemical-, physical- or biological manner
    • DE102006057975A1
    • 2007-06-06
    • DE102006057975
    • 2006-12-01
    • UNIV DRESDEN TECH
    • OSTERMANN KAIPOMPE WOLFGANGWERSING DAGMARMERTIG MICHAELGOODING JUSTINROEDEL GERHARDIHLE KAROLINA
    • C12Q1/02
    • The detection of microorganisms and/or their activity using biosensors, comprises area-wise immobilization of signal molecule ligands for binding a receptor at a surface of a substrate (1) or immobilizing the receptor for the ligands at the surface of the substrate in chemical-, physical- or biological manner. By the bonding of ligands, which are sent from the microorganisms into a process quorum of sensing, the caused physical- or physico-chemical changes detected by sensor are measurable at the receptors. The receptors are provided with a sort of- or different sorts of fluorescence markers. The detection of microorganisms and/or their activity using biosensors, comprises area-wise immobilization of signal molecule ligands for binding of a receptor at a surface of a substrate (1) or immobilizing the receptor for the ligands at the surface of the substrate in chemical-, physical- or biological manner. By the bonding of ligands, which are sent from the microorganisms into a process quorum of sensing, the caused physical- or physico-chemical changes detected by sensor are measurable at the receptors. For the production of fusion proteins or peptides by recombination techniques, amino acid sequences of receptors are changed in such a way that a change of charge, mass, light, conformation or enzymatic reaction takes place in chemical- or physical manner. The ligands are bound at the surface, the receptors are bound at the ligands and the receptors of microorganisms are delivered in the process quorum of the sensing. The receptors are separated with ligands of the medium, and the separation instrumentation is detected by the changes of the charge, mass, optical- and magnetic characteristic, charge distribution or enzymatic activity. The biosensor is calibrated by accumulation of particles at the ligands or receptors. The surface of the substrate bound with the single molecules and with the receptors, is regenerated by a repeated coating with the receptor. The fusion of proteins or the peptide is changed in such a way that the mass of the fusion protein significantly increases. The peptide is arginine, histidine or lysine for a positive net charge or the peptides contain asparagine acid or glutamine acid for a negative net charge. The receptors in their amino acid sequences are changed in such a way that an affinity between the signal molecule and the receptor is increased or decreased. The receptors are provided with a sort of- or different sorts of fluorescence markers, which are fluorescence proteins or quantum dots. The signal molecule is an autoinducer-1 (AI-1) and/or an autoinducer-2 (AI-2) and/or its combinations. The receptor is either autoinducer 2-binding periplasmic protein LuxP-molecule or a genetically produced derivative. The peptides exhibit a self-fluorescence or cause enzymatic light reaction by the addition of the substrate molecules. By the recombination techniques, an additional protein, which exhibits proteolytic-, lipolytic- or nucleolytic function, is added at the receptors to produce fusion proteins. An independent claim is included for biosensors for the detection of microorganisms and/or their activity.