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

Synthetic signal peptide and application thereof

A signal peptide and mammalian technology, applied in peptides, using vectors to introduce foreign genetic material, cells modified by introducing foreign genetic material, etc., can solve the problems of high cost and low efficiency of exogenous protein expression in animal cells, and achieve expression The effect of increasing the level, increasing the expression of foreign proteins, and reducing production costs

Active Publication Date: 2012-09-12
SHANGHAI CHEMO WANBANG BIOPHARMA +1
View PDF3 Cites 8 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the expression efficiency of exogenous protein in animal cells is low and the cost is high. Therefore, improving the expression efficiency of exogenous protein in animal cells and reducing production costs are the top priorities in current work

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
  • Synthetic signal peptide and application thereof
  • Synthetic signal peptide and application thereof
  • Synthetic signal peptide and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0048] The synthesis of embodiment 1 signal peptide

[0049] Because the signal peptide is short, the signal peptide is synthesized according to the primer. The NheI restriction site and Kozak sequence are added to the 5' end, and the target gene sequence is added to the 3' end, so as to add the signal peptide on the target gene.

[0050] Signal peptide 1: TCGGAGCTAGCCACC ATGGATGTTCTTGCTTTTCTTCTGGGCTTGCTGCTTTTGTGGCTTCCCGGGGTGAGGTGC GCCCCACCACG (SEQ ID NO: 11)

[0051] Signal peptide 2: TCGGAGCTAGCCACC ATGGATGTTCCTGCCGAATTTCTTGGATTGTTGTTGTTGTGGCTCTCCGGAGTGCGTTGC GCCCCACCACG (SEQ ID NO: 12)

[0052] Signal peptide 3: TCGGAGCTAGCC ACCATGAGGGTTCTGCCTGAATTCCTGGGACTTTTGTTGTTGTGGATTTCCGGCGTGCGATGT GCCCCACCACG (SEQ ID NO: 13)

[0053] Signal peptide 4: TCGGAGCTAGCCACC ATGGATGTACCACTTCAGCTTCTTGGCTTGTTGTTGCTTTGGCTTTCTGGCGTGAGATGT GCCCCACCACG (SEQ ID NO: 14)

[0054] Signal peptide 5: TCGGAGCTAGCCACC ATGGATGTGCCTGCTGAACTTTTGGGCCTTCTTTTGTTGTGGATATCAGGAGTACGATGC GCCC...

Embodiment 2

[0055] Embodiment 2 Amplification of the human EF-1α promoter

[0056] Using the plasmid pEF6 / V5-HisA (purchased from Invitrogen) as a template and the human EF-1α promoter sequence as a reference, primers F01 / R01 were designed and polymerase chain reaction was performed to amplify the human EF-1α promoter sequence, The reaction conditions are shown in Table 1.

[0057] F01: CATACTAGTGCTCCGGTGCCCGTCAGTGGGCAGAG (SEQ ID NO: 16)

[0058] R01: ACGGCTAGCTCCGAGCTCGGTACCAAGCTTACCTAGCCA (SEQ ID NO: 17)

[0059] Table 1 PCR reaction conditions

[0060]

[0061] The resulting PCR product was ligated with SmaI-treated pUC57 (purchased from Fermentas), and sequenced for identification. The results showed that the sequence was as follows:

[0062] ACTAGTGCTCCGGTGCCCGTCAGTGGGCAGAGCGCACATCGCCCACAGTCCCCGAGAAGTTGGGGGGAGGGGTCGGCAATTGAACCGGTGCCTAGAGAAGGTGGCGCGGGGTAAACTGGGAAAGTGATGTCGTGTACTGGCTCCGCCTTTTTCCCGAGGGTGGGGGAGAACCGTATATAAGTGCAGTAGTCGCCGTGAACGTTCTTTTTCGCAACGGGTTTGCCGCCAGAACACAGGTAA...

Embodiment 3

[0063] Embodiment 3 Amplification of the human EF1-HTLV promoter

[0064] Using the plasmid pFUSE-CHIg-hG3 (purchased from InvivoGen) as a template and the human EF1-HTLV promoter sequence as a reference, primers F02 / R02 were designed and polymerase chain reaction was performed to amplify the human EF1-HTLV promoter sequence, The reaction conditions are shown in Table 1.

[0065] F02: ACGACTAGTGCTCCGGTGCCCGTCAGTGGGCAGAGC (SEQ ID NO: 19)

[0066] R02: ATCGCTAGCGTAGGCGCCGGTCACAGCT (SEQ ID NO: 20)

[0067] The resulting PCR product was ligated with SmaI-treated pUC57 (purchased from Fermentas), and sequenced for identification. The results showed that the sequence was as follows:

[0068] ACTAGTGCTCCGGTGCCCGTCAGTGGGCAGAGCGCACATCGCCCACAGTCCCCGAGAAGTTGGGGGGAGGGGTCGGCAATTGAACGGGTGCCTAGAGAAGGTGGCGCGGGGTAAACTGGGAAAGTGATGTCGTGTACTGGCTCCGCCTTTTTCCCGAGGGTGGGGGAGAACCGTATATAAGTGCAGTAGTCGCCGTGAACGTTCTTTTTCGCAACGGGTTTGCCGCCAGAACACAGCTGAAGCTTCGAGGGGCTCGCATCTCTCCTTCACGCGCCCGCCGCCCTACCTGAGGCC...

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 relates to synthetic signal peptide and application thereof. The amino acid sequence of the signal peptide is SEQ ID NO:2. The signal peptide can be added to a mammalian cell expression vector and used for leading mammalian source protein secretion expression, and the foreign protein expression index of the signal peptide in mammalian cells can be improved.

Description

[0001] This case is a divisional application of the following patent application: [0002] Application number: 201010284904.3; [0003] Application date: September 17, 2010; [0004] Invention name: an artificially synthesized signal peptide and its application technical field [0005] The invention relates to the field of biotechnology, in particular to a signal peptide used to guide the secretion and expression of a mammalian protein in a mammalian cell and an application thereof. technical background [0006] High-efficiency expression of foreign genes in host cells is a prerequisite for protein structure and function analysis, protein or polypeptide drug research and development. The expression systems used to express recombinant proteins include microorganisms, plants, yeast, insect cells, and animal cells. Mammalian cells are the best hosts for expressing naturally active proteins, and their advantages lie in the ability to correctly and effectively recognize the sy...

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
IPC IPC(8): C07K7/08C12N15/11C12N15/85C12N5/10C12P21/02
Inventor 周永春张玉晶厉颖
Owner SHANGHAI CHEMO WANBANG BIOPHARMA
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