Nerve growth factor combined with collagen specificity and its coading gene and application
A nerve growth factor, specific binding technology, applied in the directions of nerve growth factor, growth factor/inducing factor, application, etc., can solve the problems of safety concerns, large dose, high treatment cost, etc., and achieves broad clinical application prospects and improved Viability, effect of reducing dosage
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Embodiment 1
[0031] Example 1. Cloning, Expression and Purification of Nerve Growth Factor Encoding Gene with Collagen-Specific Binding Ability
[0032] 1. Design primers
[0033] Three forward primers (CBDU, NGFU1 and NGFU2, whose sequences are shown in Table 1) and two reverse primers (CBDD and NGFD), whose sequences are shown in Table 1, were designed with the help of the software Primer premier 5.05, wherein, CBDU (restriction endonuclease Enzyme Nde I recognition site) and CBDD (introduction of restriction endonuclease Hind III recognition site) are used to amplify the coding sequence of collagen binding domain and connecting peptide (LINKER), wherein, the amino acid sequence of collagen binding domain conservation For TKKTLRT (SEQ ID №: 1 in the sequence listing), the aminoacid sequence of linking peptide is GSAGSAAGSGGK; NGFU1 (introducing restriction endonuclease Nde I recognition site) and NGFD (introducing stop codon and restriction endonuclease Xho I recognition site) is used t...
Embodiment 3
[0040] Example 3, Activity Detection of Nerve Growth Factor with Collagen-Specific Binding Ability
[0041] Rat adrenal chromaffin cells PC12 can differentiate and generate axons under the induction of NGF. In addition, NGF can promote the survival of neurons. Therefore, through PC12 (purchased from the cell bank of the Basic Medical College of Peking Union Medical College) axon induction experiments and MTT experiments Detect the activity of CBD-NGF and NAT-NGF obtained in Example 2 (Howe, C.L., Depolarization of PC12 cells induces neurite outgrowth and enhances nerve growth factor-induced neurite outgrowth in rats. Neurosci Lett, 2003.351 (1): p.41- 5.), the method is: stimulate PC12 cells with CBD-NGF and NAT-NGF at a concentration of 0-64nM, and use unstimulated PC12 cells as a control. After one day of action, PC12 cells have axon induction (see Figure 2A ); Calculate the proportion of long axon cells, the statistical results are as follows Figure 2B As shown, it can b...
Embodiment 4
[0042] Example 4, Detection of Collagen Binding Ability of CBD-NGF
[0043] Using genetic engineering technology and microbial fermentation to prepare CBD-NGF, the purpose is to enhance its binding ability to collagen three-dimensional scaffold materials for tissue engineering while ensuring its activity, so as to reduce the effective dosage of β-NGF. The improved ELISA experiments were used to detect the binding ability of NAT-NGF and CBD-NGF to collagen membrane (Finnis, M.L. and M.A. Gibson, Microfibril-associated glycoprotein-1 (MAGP-1) binds to the pepsin-resistant domain of the alpha3 (VI)chain of type VI collagen.J Biol Chem, 1997.272(36):p.22817-23.), and according to the method provided by Matsushita (Matsushita, O., et al., A study of the collagen-binding domain of a 116-kDa Clostridium histolyticum collagenase. J Biol Chem, 1998.273 (6): p.3643-8.) Calculate the dissociation constant Kd of the two proteins for collagen. Load gradually increasing doses of NAT-NGF an...
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