Abstract: The present invention relates to biologically active single chain relaxin polypeptides comprising a relaxin B chain derived from relaxin-3, the polypeptides being truncated by one or more amino acids at the C-terminus of the relaxin-3 B chain. Typically the single chain relaxin polypeptides are antagonists of the RXFP3 receptor, and in some embodiments are selective antagonists of the RXFP3 receptor.
Type:
Grant
Filed:
September 8, 2011
Date of Patent:
June 7, 2016
Assignees:
The University of Queensland, Howard Florey Institute of Experimental Physiology and Medicine
Inventors:
Karl Johan Rosengren, Linda Maria Haugaard-Kedstrom, Ross Alexander David Bathgate, Mohammed Akhter Hossain, John Desmond Wade, Andrew Lawrence Gundlach, Andrew J. Lawrence
Abstract: A method of producing projections on a patch including providing a mask on a substrate and etching the substrate using an etchant and a passivant to thereby control the etching process and form the projections, wherein the passivant does not include oxygen.
Type:
Grant
Filed:
October 7, 2014
Date of Patent:
March 15, 2016
Assignee:
The University of Queensland
Inventors:
Mark Anthony Fernance Kendall, Derek William Kenneth Jenkins
Abstract: A method is provided for inducing or enhancing an immune response in a mammal to a target polypeptide expressed in a plurality of cells of the mammal, which method comprises administering to the mammal an inhibitory nucleic acid which targets a region of a ribonucleic acid (RNA) which encodes said polypeptide. Also provided is a pharmaceutical composition comprising an inhibitory nucleic acid which targets a region of an RNA which encodes a target polypeptide expressed in a plurality of cells of a mammal, such that translation of an aberrant form of the target polypeptide occurs in said cells, said truncated form of the target polypeptide comprising one or more T cell epitopes; together with a pharmaceutically acceptable carrier or diluent.
Type:
Grant
Filed:
June 21, 2012
Date of Patent:
February 16, 2016
Assignee:
The University of Queensland
Inventors:
Nigel McMillan, Graham Leggatt, Wenyi Gu
Abstract: This invention discloses the use of an E-selectin antagonist and a mobilizer of hematopoietic stem cells or progenitor cells in methods and compositions for treating or preventing immunocompromised conditions resulting from medical treatment. The present invention is particular relevant for prophylaxis and/or treatment of hematopoeitic disorders including neutropenia, agranulocytosis, anemia and thrombocytopenia in individuals receiving or proposed to receive treatments that target rapidly dividing cells or that disrupt the cell cycle or cell division.
Abstract: The present disclosure relates to biofragment compositions that comprise bioparticle fragments and at least one heterologous antigen-binding molecule. In some embodiments, the biofragment is typically derived from a larger, intact bioparticle that express the at least one heterologous antigen-binding molecule at the surface, and the biofragment has increased solubility to facilitate assays for antigen detection. The disclosure also relates the related methods of using and making the biofragment compositions, as well as systems and devices implementing the biofragment compositions. In some embodiments, the related methods, systems and devices do not require additional detection reagents, such as animal derived detection antibodies.
Type:
Application
Filed:
December 10, 2013
Publication date:
December 31, 2015
Applicants:
Seattle Biomedical Research Institute, The University of Queensland
Inventors:
Yadveer Grewal, Gerard A. Cangelosi, Muhammad J.A. Shiddiky, Matt Trau
Abstract: A method of coating a material onto projections provided on a patch. The method includes applying a coating solution containing the material to at least the projections and drying the coating solution to at least the projections using a gas flow.
Type:
Grant
Filed:
December 23, 2008
Date of Patent:
December 29, 2015
Assignee:
The University of Queensland
Inventors:
Mark Anthony Fernance Kendall, Germain Fernando, Xianfeng Chen, Tarl Prow
Abstract: The present invention generally relates to compounds that inhibit haematopoietic-prostaglandin D2 synthase (H-PGDS), to compositions containing them and to their use in treating or preventing conditions and diseases associated with H-PGDS, such as allergies and inflammation.
Type:
Grant
Filed:
June 1, 2011
Date of Patent:
December 1, 2015
Assignee:
The University of Queensland
Inventors:
Mark Leslie Smythe, Jack Urquhart Flanagan
Abstract: The invention provides a method for preparing microparticles comprising mixing a first cross-linkable reagent in aerosol form with a second cross-linking reagent in aerosol form to thereby to form microparticles.
Abstract: The present invention relates to the use of mutant glycoproteins from pathogenic bacteria lacking one or more phosphorylcholine and/or glycosylation post-translational modifications as immunogens. These post-translational modifications act as masking structures that elicit an immune response which does not confer protection on an infected individual. The removal or modification of these masking structures alters the protein such that it elicits a stronger immune response to the protein and/or the bacterial pathogen. Particular examples are pilin proteins and nitrite reductase glycoproteins of Neisseria bacteria.
Abstract: A wastewater refinery comprising one or more electrodialytic cells with mono-, di-, or multi-valent selective membranes interspersed with one or more concentrate compartments to selectively recovery ions from wastewater. The wastewater refinery may harvest ions by utilising techniques including ion selective resins and pervaporation.
Type:
Application
Filed:
October 14, 2013
Publication date:
October 1, 2015
Applicants:
Grains Research & Development Corporation, The University of Queensland
Abstract: The invention relates to relatively short peptides (termed J-Superfamily conotoxin peptides, J-conotoxins or J-conotoxin peptides herein), about 25 residues in length, which are naturally available in minute amounts in the venom of the cone snails or analogous to the naturally available peptides, and which preferably include two disulfide bonds. The J-conotoxins are useful for treating disorders involving voltage gated ion channels and/or receptors.
Type:
Grant
Filed:
June 6, 2007
Date of Patent:
June 23, 2015
Assignees:
University of Utah Research Foundation, The University of Queensland, Max-Planck-Gesellschaft zur Foerderung der Wissenschaften e.V.
Inventors:
Julita S. Imperial, Baldomero M. Olivera, Paul F. Alewood, Heinz Terlau, David J. Craik, Estuardo Lopez-Vera, Pradip K. Bandyopadhyay
Abstract: A method for delivering a compound through a biological barrier including applying a force to a plurality of microparticles on a surface of the barrier so that at least some of the microparticles penetrate the biological barrier to facilitate delivery of the compound therethrough.
Abstract: This invention discloses methods and compositions for modulating immune responses, which involve particulate delivery of agents to immune cells, wherein the agents comprise an inhibitor of the NF-?B signaling pathway and an antigen that corresponds to a target antigen. The methods and compositions of the present invention are particularly useful in the treatment or prophylaxis of an undesirable immune response associated with the target antigen, including autoimmune diseases, allergies and transplantation associated diseases.
Type:
Grant
Filed:
October 12, 2007
Date of Patent:
April 28, 2015
Assignee:
The University of Queensland
Inventors:
Ranjeny Thomas, Nigel Meredith Davies, Brendan John O'Sullivan
Abstract: A method of forming an optical fiber tip, the method including, roughening at least part of an end portion of the optical fiber; and, etching the roughed end portion to thereby form an optical fiber tip.
Abstract: The present invention relates to designed polypeptide biosurfactants that may be prepared by recombinant technology in commercially useful amounts and purified by simple non-chromatographic methods. The designed polypeptide biosurfactants comprise at least one stimuli-responsive amino acid residue or at least one glutamine or asparagine residue and may be useful in modulating the stability of a foam, alone or in combination with an ?-helical peptide. The designed polypeptide biosurfactant may be useful in the formation and collapse of foams in foods, beverages, pharmaceuticals, personal care products, cosmetics, cleaning products, mineral recovery, bioremediation, oil recovery and laundry products. The designed biosurfactants may also be useful in recombinant production and purification of peptides, polypeptides and proteins.
Type:
Application
Filed:
December 14, 2011
Publication date:
January 29, 2015
Applicant:
The University of Queensland
Inventors:
Anton Peter Jacob Middelberg, Mirjana Dimitrijev-Dwyer, Michael Brech
Abstract: The present invention provides novel compounds of the Formula (1), pharmaceutical compositions comprising such compounds and methods for using such compounds as tools for biological studies or as agents or drugs for modulating Protease Activated Receptor-2 (PAR2) and for treating a subject at risk of—or susceptible to—a disease or disorder, or having a disease or disorder associated with undesirable PAR2 activity.
Type:
Grant
Filed:
July 28, 2011
Date of Patent:
January 6, 2015
Assignee:
The University of Queensland
Inventors:
David Paul Fairlie, Ligong Liu, Mei Kwan Yau, Jacky Yung Suen, Robert Reid
Abstract: The present invention relates to nociceptin peptide mimetics that have ?-helical structures and bind to and modulate the opioid receptor-like-1 (ORL-1) receptor. The peptide mimetics are constrained cyclic nociceptin analogs which have either agonist or antagonist activity. Pharmaceutical compositions comprising the nociceptin peptide mimetics and methods of treating or preventing a disease or condition ameliorated by modulating the ORL-1 receptor are also described.
Type:
Grant
Filed:
June 7, 2011
Date of Patent:
December 30, 2014
Assignee:
The University of Queensland
Inventors:
David Fairlie, Rosemary Sharon Harrison, Nicholas Evan Shepherd
Abstract: The present invention provides novel compounds of the Formula (1), pharmaceutical compositions comprising such compounds and methods for using such compounds as tools for biological studies or as agents or drugs for modulating Protease Activated Receptor-2 (PAR2) and for treating a subject at risk of—or susceptible to—a disease or disorder, or having a disease or disorder associated with undesirable PAR2 activity.
Type:
Grant
Filed:
July 28, 2011
Date of Patent:
December 2, 2014
Assignee:
The University of Queensland
Inventors:
David Paul Fairlie, Ligong Liu, Mei Kwan Yau, Jacky Yung Suen, Robert Reid
Abstract: A method of producing projections on a patch including providing a mask on a substrate and etching the substrate using an etchant and a passivant to thereby control the etching process and form the projections, wherein the passivant does not include oxygen.
Type:
Grant
Filed:
February 5, 2009
Date of Patent:
November 11, 2014
Assignee:
The University of Queensland
Inventors:
Mark Anthony Fernance Kendall, Derek William Kenneth Jenkins
Abstract: The present invention relates generally to methods for the prevention and treatment of acute inflammatory conditions in individuals using an agonist of the complement C3a receptor.
Type:
Application
Filed:
June 20, 2012
Publication date:
November 6, 2014
Applicant:
The University of Queensland
Inventors:
Trent Martin Woodruff, Stephen Maxwell Taylor