87 results about "Serpin" patented technology

The present invention provides methods and compositions for generating novel nucleic acid molecules through targeted spliceosomal mediated RNA trans-splicing. The compositions of the invention include pre-trans-splicing molecules (PTMs) designed to interact with a SERPINA1 target precursor messenger RNA molecule (target pre-mRNA) and mediate a trans-splicing reaction resulting in the generation of a novel chimeric RNA molecule (chimeric RNA). In particular, the PTMs of the present invention include those genetically engineered to interact with SERPINA1 target pre-mRNA so as to result in correction of SERPINA1 genetic defects responsible for AAT deficiency. The PTMs of the invention may also comprise sequences that are processed out of the PTM to yield duplex siRNA molecules directed specifically to mutant SERPIN A1 mRNAs. Such duplexed siRNAs are designed to reduce the accumulation of toxic AAT protein in liver cells. The methods and compositions of the present invention can be used in gene therapy for correction of SERPINA1 disorders such as AAT deficiency.

Methods and compositions including combined use of a serine protease inhibitor and adenosine when administered as a single pharmaceutical composition, concomitantly or sequentially in any order to a living subject for preventing organ ischemia or reperfusion injury. The methods and compositions disclosed herein can be used in such procedures as cardiac surgery, non-surgical cardiac revascularization, organ transplantation, perfusion, ischemia, reperfusion, ischemia-reperfusion injury, oxidant injury, cytokine induced injury, shock induced injury, resuscitations injury or apoptosis.

The present disclosure concerns peptides and peptidomimetics having inhibitory activity against serine proteases. The disclosed peptides and peptidomimetics are particularly useful as selective inhibitors of matriptase and MTSP1. Pharmaceutical compositions comprising serine protease inhibitors and methods for administering the compositions also are disclosed.

The invention relates to substituted polycyclic aryl and heteroaryl pyridone compounds useful as inhibitors of serine proteases of the coagulation cascade and compounds, compositions and methods for anticoagulant therapy for the treatment and prevention of a variety of thrombotic conditions including coronary artery and cerebrovascular diseases.

This invention relates to molecules, particularly polypeptides, more particularly fusion proteins that include a serpin polypeptide or an amino acid sequence that is derived from a serpin and second polypeptide comprising of at least one the following: an Fc polypeptide or an amino acid sequence that is derived from an Fc polypeptide; a cytokine targeting polypeptide or a sequence derived from a cytokine targeting polypeptide; a WAP domain containing polypeptide or a sequence derived from a WAP containing polypeptide; and an albumin polypeptide or an amino acid sequence that is derived from a serum albumin polypeptide. This invention also relates to methods of using such molecules in a variety of therapeutic and diagnostic indications, as well as methods of producing such molecules.

ATIII is a serine proteinase inhibitor (serpin) with anti-coagulant, anti-inflammatory, anti-proliferative and anti-angiogenic properties. The invention features methods of treating a subject having lung injury due to burns and smoke inhalation by administering a synergistic combination of antithrombin III and heparin through pulmonary delivery means.

The invention relates to a composition capable of whitening and brightening, a preparation method thereof and an application thereof in cosmetics and belongs to the technical field of the cosmetics. The composition capable of whitening and brightening comprises the following ingredients in percentage by weight: 25% to 30% of arbutin, 10% to 15% of vitamin C or derivative thereof, 15% to 20% of nicotinamide, 3% to 6% of serpin, 1% to 2% of ginsenoside and 30% to 35% of sunscreen agent. According to the composition provided by the invention, the arbutin, the vitamin C derivative and the nicotinamide generate a whitening effect, and meanwhile, the serpin is used for protecting protein components of skin cells, promoting the activation and regeneration of the cells and eliminating cytotoxicity resulting from hydroquinone generated after the arbutin is reduced, so that the actions of long-acting whitening and cell activating are achieved; the composition has the advantages of little skin irritation and long acting time when the composition is applied to the cosmetics such as facial masks, emulsions and cream.

The invention relates to substituted polycyclic aryl and heteroaryl pyrazinone compounds useful as inhibitors of serine proteases of the coagulation cascade and compounds, compositions and methods for anticoagulant therapy for the treatment and prevention of a variety of thrombotic conditions including coronary artery and cerebrovascular diseases.

The invention is directed to biomarkers for determining the EGFR kinase activity in a subject, and the use thereof for predicting and monitoring therapeutic intervention in cancer patients. Areas of application are the life sciences: biology, biochemistry, biotechnology, medicine and medical technology.

The biomarkers are selected from a first group consisting of Amy 1, Apo Al, Carbx, Casp, AFP, ApoM, SAP, Fib-a, Fib-b, Fib-g, ApoE, A2MG, A2MG isoform, Serpin, Clusterin, MHC-fB, SAP isoform, or from a second group consisting of Gpx3, properidin, MUP1, HMW-K, Lifr-p, Orm 1, MBL-A, MBP-C, wherein the biomarkers are regulated by EGF overexpression in a subject.

This invention describes a relevant etiology of cancer and a novel anti-cancer therapeutic strategy, based on the discovery that a protein named serine protease inhibitor (SPIK/SPINK/PSTI) was up-regulated by hepatitis B and C virus infections consequently suppressing the cell apoptosis. Accordingly, this invention provides an inhibitor of SPIK and/or a technology of suppression of over-expression of SPIK in cells. The inhibitors include: 1) chemical compounds, which can inhibit SPIK transcripts, protein activity, and gene expression, 2) SPIK siRNA (RNAi gene silence or dsRNA of SPIK, 3) DNA anti-sense and anti-SPIK antibody. Further, this invention provides a method of using the inhibitor as an anti-cancer agent to re-instate cancer cell apoptosis (e.g., serine protease dependent cell apoptosis). Also provided is an anti-SPIK antibody specific for an epitope comprising the first nine amino acids of intact SPIK. Further, a diagnostic kit is provided comprising at least one antibody specific for an epitope comprising the first nine amino acids of intact SPIK to diagnose patients exhibiting disease symptoms or at risk for developing a disease, wherein the disease is HBV infection, HCV infection, hepatitis, cancer or hepatic cancer.

The invention belongs to a method for purifying natural serine protease inhibitors, which comprises the steps of silkworm pupa pretreatment, primary separation purification of the natural serine protease inhibitors, and the separation purification of the natural serine protease inhibitors. The method has the advantages that silkworm pupas are used as raw materials, the natural serine protease inhibitors with the medicinal value in the silkworm pupas are obtained through separation and purification, the method is simple and convenient to operate, the yield is high, the method is suitable for large-scale production, the purified natural serine protease inhibitors can be used as health-care medicine, and no toxic or side effect is caused.

The present invention relates to the general field of therapy of Inflammatory Bowel Disease (IBD) and/or Irritable Bowel Syndrome (IBS). Thus, the invention relates to a molecule selected from the trappin-2 protein or an active fraction thereof, a member of the WAP family proteins or an active fraction thereof or a member of the Serpin family proteins or an active fraction thereof for the treatment of Irritable Bowel Syndrome (IBS). The invention also relates to a recombinant food-grade bacterium comprising a gene selected from a gene coding for the trappin-2 protein or an active fraction thereof, a gene coding for a member of the WAP family proteins or an active fraction thereof, or a gene coding for a member of the Serpin family proteins or an active fraction thereof.

The present invention provides novel polynucleotides encoding LSI-01 polypeptides, fragments and homologues thereof. Also provided are vectors, host cells, antibodies, and recombinant and synthetic methods for producing said polypeptides. The invention further relates to diagnostic and therapeutic methods for applying these novel LSI-01 polypeptides to the diagnosis, treatment, and/or prevention of various diseases and/or disorders related to these polypeptides. The invention further relates to screening methods for identifying agonists and antagonists of the polynucleotides and polypeptides of the present invention.

The invention discloses an autism serum polypeptide marker SERPINA5-A and the application thereof. The amino acid sequence of the marker is shown in SEQ.ID.NO.1. The molecule is called SERPINA5-A and is one fragment of SERPINA5, the exact molecular weight of the molecule is 3886 Daltons, SERPINA5-A is remarkably highly expressed in autism children sera diagnosis, and a method for detecting SERPINA5-A or ELISA by means of a matrix assisted laser desorption/ionization time-of-flight mass spectrometer (MALDI-TOF-MS) is used for detecting the expression level of SERPINA5 and can be used as an autism serum detection method.

The invention relates to the technical field of bio-medicine and relates to a structure of serpin-3, an obtaining method and new physiological functions of the serpin-3 and application in the field of bio-medicine. The amino acid and nucleotide sequence of complete sequences of the serpin-3 is shown in SEQ ID NO:1. The amino acid and nucleotide sequence of mature peptide of the serpin-3 is shown in SEQ ID NO:2. The invention further provides an analogue or active fragments of the recombinant serpin-3. The natural and recombinant serpin-3 and the analogue and part of fragments of the serpin-3 have an inhibition effect on serine protease, antimicrobial peptide synthesis and a system activating prophenoloxidase in vitro and vivo. The obtaining method of the natural and recombinant serpin-3 and the part of fragments or analogue of the serpin-3 is conventional, simple and high in yield.