Novel Cedar Pollen Protein
A technology of pollen and fir tree, applied in peptide/protein components, anti-plant immunoglobulin, allergic diseases, etc., can solve the problems of ineffective allergen immunotherapy and achieve the effect of effective desensitization treatment
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Embodiment 1
[0100] The rough refinement of embodiment 1 novel fir tree pollen protein
[0101]
[0102] 50 mL of an extraction buffer (20 mM Tris-HCl, pH 9.0) was added to 2 g of cedar tree pollen, and ultrasonication was performed for 10 minutes. Next, after mixing at room temperature for 10 minutes, it was centrifuged (10,000 g, 10 minutes) to obtain a supernatant. This supernatant was again subjected to ultracentrifugation (50,000 g, 60 minutes), and the supernatant was collected. To 17 mL of this supernatant, an equal amount of Q sepharose high performance resin (GE Healthscare) suspension equilibrated with an extraction buffer (20 mM Tris-HCl, pH 9.0) was added, followed by shaking at room temperature for 30 minutes. After the supernatant was removed by centrifugation (1,000 g, 10 minutes), the volume was adjusted to 50 mL with extraction buffer (20 mM Tris-HCl, pH 9.0), mixed by inversion, and the resin was washed by centrifugation again. Next, 10 mL of an extraction buffer (20 ...
Embodiment 2
[0105] Embodiment 2 Preparation of refined recombinant protein
[0106]
[0107] To a 50 mL tube containing 25 mL of Plant RNA Isolation Reagent (Invitrogen), 2 g of cedar tree male flowers (anthers) frozen and ground in liquid nitrogen were added, mixed, and left to stand at room temperature for 5 minutes.
[0108] After centrifugation at 4° C. (2600×g, 5 minutes), the upper layer was filtered through a mesh with a mesh size of 100 μm by decantation. Next, 1 / 5 times the amount of 5M NaCl and 3 / 5 times the amount of chloroform were added to the recovered filtrate. After centrifugation at 4° C. (2600×g, 30 minutes), 20 mL of the upper layer was recovered, and 9 / 10 times the amount of isopropanol was added and stirred. After standing still at room temperature for 10 minutes, the RNA was precipitated by centrifugation at 4°C (2600 x g, 30 minutes). After removing the supernatant, 10 mL of 75% ethanol was added to the RNA pellet for washing. Then, after centrifugation at 4° C...
Embodiment 3
[0116] Example 3 Allergen Activity Confirmation of Refined Recombinant Protein
[0117] (i) Lymphocyte proliferation response in patients with cedar tree hay fever
[0118] Peripheral blood mononuclear cells were isolated from 30 mL of peripheral blood obtained from cedar hay fever patients (ImmunoCAP score ≥ 2) to become 1.11×10 6 cells / mL were suspended in RPMI-1640 medium containing 10% non-activated autologous plasma. Inoculate 180 μL of the prepared cell suspension and 20 μL of the recombinant protein solution (concentration 100 μg / mL) of the present invention on a 96-well plate (2×10 5 cells / well). At 37°C, 5% CO 2 After culturing for 3 days under the condition, add 3 For H-thymidine, the uptake amount after 16 hours was measured as radioactivity, thereby evaluating cell proliferation. Calculate the time when adding purified recombinant protein 3 The value obtained by dividing the intake of H-thymidine by the intake when it was not added was used as a stimulation i...
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