Dipurification process of recombinant humangranulocyte colony stimulating factor
A colony-stimulating factor and granulocyte technology, applied in recombinant DNA technology, growth factor/inducing factor, organic chemistry, etc., can solve the problems of existence of isomers, renaturation yield, complex preparation process, etc.
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Embodiment 1
[0018] Example 1: Acquisition of rhG-CSF high-purity inclusion bodies
[0019] After fermenting rhG-CSF genetically engineered bacteria (provided by North China Pharmaceutical Jintan Biotechnology Co., Ltd.), take 1 kg of wet bacteria and wash with PBS buffer (60mmol / L PB, 150mmol / L NaCl, 1mmol / LEDTA, pH 7.0) , wash away impurities such as the unutilized medium carried in the thalline, centrifuge at 8000g (Avanti J-25, Beckman company), collect the precipitate, and then put it in the above solution again, under the condition that the solid-liquid ratio is 1:10 , mixed into a uniform suspension, pumped into a high-pressure homogenate pump for high-pressure homogenate crushing (APV30-30CD, APV GAULIN Company), and then obtained 120 g of wet crude inclusion bodies by centrifugation.
[0020] The crude inclusion bodies obtained above were mixed with buffer A (urea 4mol / L, Tris-HCl 20mmol / L, EDTA10mmol / L, TritonX-100 0.2%, pH8.0) and buffer B (Tris-HCl 50mmol / L, EDTA10mmol / L, pH8....
Embodiment 2
[0021] Example 2: Lysis of rhG-CSF inclusion bodies
[0022] Take 5 g of high-purity inclusion bodies, cleavage with lysate (8mol / L Urea, 100mmol / L Tris-HCl, 5mmol / L DTT, 2mmol / L EDTA) at a solid-liquid ratio of 1:100, and stir gently at room temperature for 2-3 Hours, centrifuged to obtain 510ml supernatant, and the protein concentration was determined by the Lowry method.
[0023] The lysate was subjected to SephadexG-25 separation to remove excess reducing agent DTT.
Embodiment 3
[0024] Example 3: Refolding of rhG-CSF inclusion bodies
[0025] Component
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