Photosensitizer binding protein/polypeptide and application thereof to photodynamic gene therapy

A technology for binding proteins and photosensitizers, which is applied in the field of photosensitizers binding proteins and peptides, and can solve problems such as unclear mechanisms

Inactive Publication Date: 2011-09-07
FUDAN UNIV
View PDF4 Cites 5 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

As for the mechanism of photosensitizer enrichment in tumor cells is not very clear, resulting in PDT curative effect is limited by the difference in enrichment state of photosensitizer in tumor and normal tissue and its passive target diffusion state

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
  • Photosensitizer binding protein/polypeptide and application thereof to photodynamic gene therapy
  • Photosensitizer binding protein/polypeptide and application thereof to photodynamic gene therapy
  • Photosensitizer binding protein/polypeptide and application thereof to photodynamic gene therapy

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0044] PCR amplification of exogenous phage genes

[0045] Using the phage combined with the photosensitizer screened from the human liver cDNA phage display library as described in the patent 2010105533095 as the PCR reaction template, the forward primer T7SelectUP Primer and the reverse primer T7SelectDOWN Primer were used for PCR amplification to obtain T7 Carrier exogenous gene PCR product.

Embodiment 2

[0047] Gene Blast analysis of photosensitizer-bound phage

[0048] 1. After the above-mentioned PCR products were connected with the pMD-19T vector, transform and clone the strain XL1-Blue, pick 5-10 transformants and culture them, and screen the positive transformants by PCR cloning in bacterial solution, send them to Handsome Shanghai Biological Co., Ltd. for sequencing, and analyze the T7Select vector. See SEQ ID NO.1 for the foreign insert sequence.

[0049] 2. The exogenous insertion sequence of the T7Select vector was analyzed by NCBI Blast, and it was confirmed that the 362 bases of the exogenous gene were completely consistent with the 1374-1735 base sequence of the eEF1A1 full-length gene, and the coding gene was 1374-1452, and the inserted sequence was consistent with the vector The fused ORF is consistent with the C-terminal 25aa of the amino acid sequence encoded by an ORF of eEF1a1, and the specific sequence information of 25aa is shown in SEQ ID NO.2.

Embodiment 3

[0051] Obtaining of eEF1A1 Genetic Engineering Protein

[0052] Obtained as described in the patent 201010504169.2, the protein sequence information is shown in SEQ ID NO.3.

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

PropertyMeasurementUnit
molecular weightaaaaaaaaaa
Login to view more

Abstract

The invention belongs to the technical field of photodynamic gene therapy, particularly relating to a photosensitizer binding protein and polypeptide and application thereof. In the invention, the photosensitizer binding protein is screened from a human liver cDNA (complementary Deoxyribonucleic Acid) phage display library. The binding protein is a human eukaryotic translation elongation factor (eEF1A1) protein and a protein molecule which is 70 to 80 percent similar to the protein in protein structure; the photosensitizer binding polypeptide is eEF1A1 C terminal 25aa and polypeptide which is70 to 80 percent similar to the 25aa in amino acid sequence. The photosensitizer binding protein can be bound with a porphyrin type photosensitizer in vitro and has an effect of enriching the porphyrin type photosensitizer in vivo; photosensitizer binding protein genes are transfected to various mammalian cells through adenoviruses, slow viruses or other modes; and a better photodynamic therapy effect is produced after artificial adjustment and control over inducible expression. In addition, the photosensitizer binding protein and polypeptide (PSP) provide a valuable reference for developing a photosensitizer prodrug and designing the specifically targeted photosensitizer.

Description

technical field [0001] The invention belongs to the technical field of photodynamic therapy, in particular to a photosensitizer binding protein and peptide (Photosensitizer binding Protein & Peptide, PBP for short) and its application. The present invention mainly relates to the binding protein (PBPr) of porphyrin photosensitizer is eEF1A1 protein and a protein molecule with more than 70% homology with the protein sequence, and the photosensitizer-binding polypeptide (PBPe) is a 25aa residue peptide and its amino acid sequence Peptides with more than 70% homology. However, eEF1A1 is specifically highly expressed in some tumors within the scope of photodynamic therapy, such as colon cancer, bladder cancer, esophageal cancer, skin cancer and breast cancer, which provides a source for the specific enrichment of photosensitizers in tumor cells during photodynamic therapy. A reasonable explanation provides a valuable reference for the development of photosensitizer prodrugs and th...

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): C12N7/01C12N15/67C07K14/47A61K38/17A61K41/00A61K48/00A61K47/42A61P35/00
Inventor 朱乃硕魏勋斌郭艳荣
Owner FUDAN UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products