Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Tat PTD-Endostatin-RGD recombinant protein and preparation method and application thereof

A recombinant protein and transduction protein technology, applied in the fields of peptide/protein components, chemical instruments and methods, recombinant DNA technology, etc., can solve the problem of no fusion expression, improve targeting and residence time, and eliminate the need for enzyme digestion The effect of recovery, rapid DNA ligation reaction

Active Publication Date: 2016-01-06
SHANDONG UNIV
View PDF3 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] However, there are still a series of technical difficulties in combining target proteins with different activities for fusion expression, such as whether different proteins can still have the original activity after integration, the choice of fusion protein expression system, etc. Therefore, there is currently no A report on the fusion expression of TatPTD, Endostatin and RGD

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Tat PTD-Endostatin-RGD recombinant protein and preparation method and application thereof
  • Tat PTD-Endostatin-RGD recombinant protein and preparation method and application thereof
  • Tat PTD-Endostatin-RGD recombinant protein and preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0052] Embodiment 1: Preparation of TatPTD-Endostatin-RGD fusion protein

[0053] 1. The construction of fusion gene: adopt the method for PCR to obtain fusion gene with TatPTD-Es as template (results see Figure 1a-Figure 1b ), and recycle.

[0054] 2. Double digestion of the empty plasmid pET28a: the E. coli expression plasmid pET28a was double digested with BamHI and XhoI, and the fragments were recovered.

[0055] 3. Ligation of the fusion gene and the plasmid: Add 100 ng of the recovered product from PCR and 100 ng of the product recovered from the digestion of the empty plasmid into the Gibson polymerization ligation reaction system, react at 50°C for 1 h, and the ligated product is used for the next transformation.

[0056] 4. Transformation of recombinant plasmids: quickly add 6 μl of the above ligation solution to 100 μl of pre-cooled competent cells E.coliDH5α and mix well, ice-bath for 30 minutes, heat shock at 42°C for 90 seconds, ice-bath for 2-3 minutes, add 900...

Embodiment 2

[0065] Example 2: Research on the biological activity of TatPTD-Endostatin-RGD fusion protein

[0066] Investigate the activity of TatPTD-Es-RGD in inhibiting the proliferation of endothelial cells: with Es, TatPTD-Es, Es-RGD as the control (the other three proteins used as the control here are prepared in the same way as TatPTD-Es-RGD), using CCK- 8 method to investigate the activity of purified TatPTD-Es-RGD in inhibiting the proliferation of vascular endothelial cells, the specific implementation steps are as follows:

[0067] The cryopreserved solution of human umbilical vein endothelial cells (EAHY926) was quickly thawed in a 37°C water bath, centrifuged at 800r / min for 3min, and the supernatant was discarded. Resuspend the cell pellet with sterile PBS, centrifuge at 800r / min for 3min, and discard the supernatant. The cell pellet was resuspended with DMEM medium (containing 10% FBS) and blown evenly to form a cell suspension, and the cell count was performed on a cell co...

Embodiment 3

[0070] Example 3: Inhibition of TatPTD-Es-RGD on Chick Embryo Chorioallantoic Membrane Angiogenesis (CAM) Generation

[0071] 1. Test method:

[0072] 1.1 The method of incubating CAM: the method is as follows: select well-growth white preserved eggs from breeder farms with a fertilization rate greater than 90% (clean and smooth surface, uniform size, standard egg shape, uniform stomata and air cells), and use them after cleaning. 1‰ benzalkonol was used to wipe and disinfect the shell of the eggs, and the eggs were cultured in an insulated electric heating constant temperature incubator at a temperature of (38±1)°C and a humidity of 60-80%, with certain ventilation condition. The air cell of the egg is upward, and the long axis is at an angle of about 70°-80° to the egg tray. Turn the egg 3 times a day, and the angle of the egg turning should be 45° in the horizontal position. After the eggs were incubated for 5 days, the eggs were illuminated with an egg lamp, and well-de...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses Tat PTD-Endostatin-RGD recombinant protein which is composed of the protein transduction domain of transactivation transduction protein Tat of human immunodeficiency viruses, the human endostatin and RGD tripeptide coming from the fiber cell attachment domain. The invention further discloses a preparation method of the Tat PTD-Endostatin-RGD recombinant protein, and application of the Tat PTD-Endostatin-RGD recombinant protein to medicine for treating diseases caused by new vessels and medicine for restraining endothelial cell migration. The Tat PTD-Endostatin-RGD recombinant protein reserves the activity of endostatin for restraining new vessel proliferation, and can penetrate through blood brain barriers or eyeball barriers to be combined with integrin specificity over-expressed at new vessels, the targeting performance of the fused protein is greatly improved, and the retention time of the fused protein is greatly prolonged.

Description

technical field [0001] The invention relates to a TatPTD-Endostatin-RGD recombinant protein and its preparation method and application, belonging to the technical field of biomedicine. Background technique [0002] Endostatin (Endostatin, Es) is an endogenous angiogenesis inhibitor isolated from hemangioendothelioma by O'Reilly et al. in 1997. Endostatin is a fragment of the C-terminus of collagen XVIII molecule, with a total of 184 amino acid residues and a molecular weight of 20kDa. Studies have shown that endostatin can only inhibit the formation of new blood vessels but not the existing blood vessels. Endostatin is currently the most effective tumor angiogenesis inhibitor with the best experimental effect. It has attracted much attention in recent years. At present, phase I and phase II clinical trials have been carried out in the United States. A class of new drug Endostar (Endostar) with national independent intellectual property rights has been developed for the tre...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C07K19/00C12N15/62C12N15/70A61K38/39A61K47/48A61P35/00A61P9/10
Inventor 王凤山李妍生举正冯丹阳
Owner SHANDONG UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com