Patent classifications
C07K14/5759
RECOMBINANT IRISIN GENE OPTIMIZED FOR EXPRESSION IN PLANTS AND METHOD FOR PRODUCING RECOMBINANT IRISIN PROTEIN USING SAME
The present invention relates to a recombinant irisin gene optimized for expression in plants and comprising a nucleotide sequence represented by SEQ ID NO: 1, a method for producing an irisin protein, and a composition for preventing or treating metabolic diseases, comprising same.
Weight loss regimen
Obesity and/or diabetes are treated by partially inhibiting circulating leptin in a person in need thereof.
LEPTIN IMMUNOGENS, HYBRIDOMA CELLS, MONOCLONAL ANTIBODIES, POLYCLONAL ANTIBODIES AND USE THEREOF
Provided are a leptin immunogen, hybridoma cells, a monoclonal antibody, a polyclonal antibody and use thereof. The leptin immunogen comprises a polypeptide having an amino acid sequence as shown in SEQ ID NO: 1. The anti-leptin monoclonal antibody prepared with the leptin immunogen has good specificity and high sensitivity.
Oncolytic Immunotherapy by Tumor Micro-Environment Remodeling
The disclosure relates to modified oncolytic viruses. The modified oncolytic viruses of the disclosure comprise modification in the viral genome encoding exogenous nucleic acids to enhance the oncolytic immunotherapy by remodeling the tumor microenvironment and with enhanced systemic delivery. The disclosure further relates to compositions comprising the modified oncolytic viruses, kits containing the same, and methods of using the oncolytic viruses.
Peptide with anti-obesity and anti-diabetes activity and use thereof
A peptide and a peptide complex of the present invention exhibit an anti-obesity effect by inhibiting fat accumulation and decomposing already accumulated fat, and exhibit an excellent effect with respect to diabetes by effectively reducing blood sugar. The peptide and the peptide complex of the present invention decrease the expression of PPARγ, ACC, and aP2, which are adipogenic markers, increase the expression of pHSL, AMPK-α1, CGI-58, and ATGL, which are lipolytic factors, and reduce the size of fat cells and blood cholesterol values. The peptide and the peptide complex of the present invention, which have excellent activity and safety, can be advantageously applied to drugs and quasi-drugs.
Combinatorial gene construct and non-viral delivery for anti-obesity
The invention provides a plasmid comprising two or more anti-obesity genes. Also provided by the invention are compositions and host cells comprising the plasmid and methods of increasing the metabolic activity in a mammal. The invention provides a plasmid comprising two or more of (a) a nucleic acid sequence encoding islet amyloid polypeptide (IAPP), (b) a nucleic acid sequence encoding leptin (LEP), and (c) a nucleic acid sequence encoding fibronectin type III domain containing 5 (FNDC5).
METHOD FOR EXTENDING HALF-LIFE OF A PROTEIN
The present invention relates to a method for prolonging half-life of a protein or a (poly)peptide by replacing one or more amino acid residues of the protein. Further, the present invention is about the protein having a prolonged half-life prepared by the method above.
Expression of metabolic modulators in tumor microenvironment to improve tumor therapy
Recombinant oncolytic viruses (OVs) that express one or more metabolic modulator proteins, such as an adipokine (e.g., leptin or chemerin), insulin, and/or IGF-1, and methods of their use to treat cancer, for example in immunotherapy anti-cancer treatments. In some examples, such recombinant OVs and methods increase T cell infiltration into the tumor or tumor microenvironment.
METHOD FOR EXTENDING HALF-LIFE OF A PROTEIN
The present invention relates to a method for prolonging half-life of a protein or a (poly)peptide by replacing one or more amino acid residues of the protein. Further, the present invention is about the protein having a prolonged half-life prepared by the method above.
METHOD FOR EXTENDING HALF-LIFE OF A PROTEIN
The present invention relates to a method for prolonging half-life of a protein or a (poly)peptide by replacing one or more amino acid residues of the protein. Further, the present invention is about the protein having a prolonged half-life prepared by the method above.