摘要:
The present invention relates to a field of biological pharmacy, wherein a fusion protein rLZ-8 of a ganoderma immunoregulatory protein and HSA prepared with gene engineering technologies, a preparation method thereof and applications thereof are disclosed. Compared with rLZ-8, a half-life of the fusion protein is prolonged, and biological activity thereof is increased. The fusion protein is applicable to drugs in treatment of leucopenia and anti-tumor.
摘要:
An application of a recombinant immunoregulatory protein of ganoderma lucidum (rLZ-8) expressed by Pichia pastoris in a preparation of a drug for treating focal cerebral ischemia is provided. The rLZ-8 is able to treat a neurological function injury, decrease a neurological severity score caused by a cerebral injury and decrease an ED-1 positive cell number, so as to decrease an inflammatory response and inhibit apoptosis.
摘要:
Embodiments of the present disclosure provide apparatuses and methods for determining a compacting arrangement to store logical addressable units, which include compressed data sectors, into hardware addressable units of a storage device. The compacting arrangement is based on compression information associated with the logical addressable units. A write module is used to write the compressed data sectors to the storage device according to the compacting arrangement.
摘要:
The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5A inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5A activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.
摘要:
Apparatus comprising a source of optical radiation (15), an optical fibre (1), and an absorbing material (2), wherein; the optical fibre (1) comprises a core (37), at least one cladding (38), and an optical surface (3); the source of optical radiation (15) provides optical radiation (16) that propagates along the core (37) of the optical fibre (1), and unwanted optical radiation (14) that propagates along the cladding (38) that surrounds the core (37); and the absorbing material (2) is in contact with the optical surface (3) over a length (5) of the optical fibre (1). The apparatus is characterized in that: the absorbing material (2) has a refractive index (101) that is higher than a refractive index (100) of the optical surface (3) within a temperature range (102) thus enabling the unwanted optical radiation (14) to pass from the optical fibre (1) into the absorbing material (2) within said temperature range (102); the absorbing material (2) is such that it can absorb at least some of the unwanted optical radiation (14) that enters into it from the optical fibre (1); the absorbing material (2) is such that its temperature increases upon absorption of the unwanted optical radiation (14); and the absorbing material (2) is such that its said refractive index (101) reduces with increasing temperature. This has the effect of limiting the amount of the unwanted optical radiation (14) that can be removed per unit length of optical fibre (1) to a predetermined absorption per unit length (62). Thus the apparatus is such that it is able to remove the unwanted optical radiation (14) up to a power level (12) substantially equal to the product of the predetermined absorption per unit length (62) and the length (5) over which the absorbing material (2) is in contact with the optical surface (3).
摘要:
The present invention provides methods and compositions for enhancing channel activity to the mutant cystic fibrosis trans-membrane conductance regulator protein (CFTR). The compositions of the invention comprise polypeptides containing CFTR sub-domains that are designed to mimic the folding defect of the full length mutant CFTR proteins, resulting in competitive binding to cytoplasmic chaperones such as Hsc/Hsp70 and Hdj2. The methods of the invention comprise transduction, or recombinant expression, of CFTR polypeptides in a cell expressing mutant CFTR. The presence of the CFTR polypeptide results in a dominant effect whereby the CFTR polypeptide competes with the endogenously expressed mutant CFTR for binding to cytoplasmic chaperones such as Hsc/Hsp70 and Hdj2. Mutant CFTR proteins include, but are not limited to, ΔF508 CFTR. The present invention is based on the discovery that reduced binding of cytoplasmic chaperones to the endogenous ΔF508 CFTR, mediated by the presence of CFTR polypeptides, results in restoration of plasma membrane localization and channel activity. The methods and compositions of the invention can be used to restore channel activity in cystic fibrosis subjects carrying genetic defects in the CFTR gene, such as for example, ΔF508 CFTR.
摘要:
The present invention relates to novel Tetracyclic Xanthene Derivatives of Formula (I) and pharmaceutically acceptable salts thereof, wherein A, Y1, Y2, Z, Ra, Rb, R1a, R1b and R2 are as defined herein. The present invention also relates to compositions comprising at least one Tetracyclic Xanthene Derivative, and methods of using the Tetracyclic Xanthene Derivatives for treating or preventing HCV infection in a patient.
摘要:
A use of recombinant ganoderma immunoregulatory protein (rLZ-8) in a preparation of a drug for treating melanoma is disclosed. By establishing experimental animal models of orthotopic tumors and metastatic tumors, an anti-tumor effect of the rLZ-8 is researched, which indicates that the rLZ-8 significantly inhibits a growth of the orthotopic tumors of the melanoma and a formation of metastases of the melanoma.
摘要:
Mutants of recombinant immunoregulatory protein of Ganoderma lucidum (rLZ-8) and applications thereof are provided. It is found by the present invention that: an anti-EGFR (epidermal growth factor receptor) domain exists in a structure of the rLZ-8; particularly, the domain through positive potential characteristics thereof induces a killing effect to an abnormal EGFR-expressed tumor. Based on the above scientific discovery, with utilizing computational simulation technology, the mutants of the rLZ-8, having better antitumor effects, are obtained.