Polyethylene glycol modified human thymosin beta 4 tandem repeat protein, as well as preparation method and application thereof
A technology of polyethylene glycol and methoxypolyethylene glycol, which is applied in the field of preparation of human thymosin β4 dimer protein, which can solve the problems of unfavorable prokaryotic expression system expression and purification, inability to produce on a large scale, and synthesis efficiency Low-level problems, to achieve the effect of promoting wound healing, promoting the proliferation of cardiomyocytes, and preserving the activity
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Embodiment 1
[0068] Example 1 Preparation of Human Thymosin β4 Ditandem Protein (rTβ4)
[0069] 1. Construction of pET-28a(+)-rTβ4
[0070] Fusion of human thymosin β4 with HKDCDI gene sequence, GS linker gene sequence, 6*His tag gene sequence, and after codon preference optimization, a new gene sequence (shown in SEQ ID NO.1) is formed. The connection sequence is: HKDCDI gene sequence-Thymosin β4 gene sequence-GS Linker GSGSG-Thymosin β4 gene sequence-6*His tag gene sequence, the gene sequence is chemically synthesized with NcoI (enzyme cutting site CCATG / G to avoid When the frameshift gene is synthesized, the base G) and XhoI (C / TCGAG) are removed as the restriction site and cloned into the expression vector pET-28a(+) by homologous recombination to obtain the recombinant plasmid pET-28a(+)-rTβ4. The gene sequence synthesized by codon optimization after recombination is:
[0071]
[0072] among them:
[0073] NcoI and XhoI restriction sites are CCATG, CTCGAG
[0074] The HKCDI gene sequence i...
Embodiment 2
[0093] Example Preparation of di-polyethylene glycol modified human thymosin β4 distrand protein (PEG-rTβ4)
[0094] The PEG-rTβ4 (n=2000, n=12000, n=20000) protein prepared in the present invention includes the following steps:
[0095] 1. Combine the obtained rTβ4 protein with methoxy polyethylene glycol maleimide (hereinafter referred to as mPEG 2000 -MAL, mPEG 12000 -MAL, mPEG 20000 -MAL) and tris(2-carboxyethyl)phosphine (hereinafter referred to as TCEP) according to 1:1:4, 1:15:6, 1:40:8 (w:w:w) dissolved in PBS (pH8.0 ), each milliliter of PBS solution contains rTβ4 protein, mPEG n- MAL and TCEP are respectively 1mg, 1mg, 4mg, 1mg, 15mg, 6mg, 1mg, 40mg, 8mg, 8℃ shaker (200rpm / min) reaction overnight;
[0096] 2. The reaction product was replaced with PBS (pH 8.0) by a dialysis device, and PEG-rTβ4 protein was purified with AKTA Prime Plus; firstly, the gel column was fully equilibrated with PBS (pH 8.0) with 5 column volumes, and then The protein solution prepared in the prev...
Embodiment 3
[0102] Example 3 MALDI-TOF molecular weight determination of rTβ4 protein and PEG-rTβ4 (n=2000) protein
[0103] In this experiment, the freeze-dried powder of rTβ4 protein and PEG-rTβ4 protein was mailed to Shanghai Zhongke New Life Biotechnology Co., Ltd. for MALDI-TOF molecular weight determination. The results showed that the determination results were consistent with the expected molecular weight and purity of rTβ4 protein and PEG-rTβ4 protein. Higher (see Picture 10 , Picture 11 ).
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