2003Zhonghua weishengwuxue he mianyixue zazhiRequires access

Specific c7c TNF-α mimotope phage clone as target for screening TNF-α specific binding-peptides from 12mer phage display peptide library

FU Nin

Open publisher page 0 citations

Abstract

Objective By using specific c7c TNF-α mimotope displayed on phage as a target, we got specific TNF-α binding-peptides clones from 12mer phage display peptide library and developed a novel approach for screening phage peptide library. Methods Using c7c TNF-α mimotope phage clones LCS-7 (c-RRPAQSG-c) as a target to screen 12mer phage peptide library and identify the positive clones by phage ELISA and competive ELISA. Results After 3 rounds of screening, 10 of 20 clones were identified as positive clones and all the 10 phage clones shared the identical amino acid sequence: EHMALTYPFRPP. Conclusion The positive 12mer phage clone peptide screened with cycle 7mer TNF-α simulating phage clone as a target can bind to TNF-α specifically. The results suggest that this method is very specific and easy- for screening of binding epitope from phage display peptide library. [

About this research paper

What this paper is about

Objective By using specific c7c TNF-α mimotope displayed on phage as a target, we got specific TNF-α binding-peptides clones from 12mer phage display peptide library and developed a novel approach for screening phage peptide library. Methods Using c7c TNF-α mimotope phage clones LCS-7 (c-RRPAQSG-c) as a target to screen 12mer phage peptide library and identify the positive clones by phage ELISA and competive ELISA. Results After 3 rounds of screening, 10 of 20 clones were identified as positive clones and all the 10 phage clones shared the identical amino acid sequence: EHMALTYPFRPP. Conclusion The positive 12mer phage clone peptide screened with cycle 7mer TNF-α simulating phage clone as a target can bind to TNF-α specifically. The results suggest that this method is very specific and easy- for screening of binding epitope from phage display peptide library. [

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective By using specific c7c TNF-α mimotope displayed on phage as a target, we got specific TNF-α binding-peptides clones from 12mer phage display peptide library and developed a novel approach for screening phage peptide library. Methods Using c7c TNF-α mimotope phage clones LCS-7 (c-RRPAQSG-c) as a target to screen 12mer phage peptide library and identify the positive clones by phage ELISA and competive ELISA. Results After 3 rounds of screening, 10 of 20 clones were identified as positive clones and all the 10 phage clones shared the identical amino acid sequence: EHMALTYPFRPP. Conclusion The positive 12mer phage clone peptide screened with cycle 7mer TNF-α simulating phage clone as a target can bind to TNF-α specifically. The results suggest that this method is very specific and easy- for screening of binding epitope from phage display peptide library. [

Key concepts: Mimotope, Phage display, Peptide library, Peptide, clone (Java method), Molecular biology, Biology, Phagemid

Related papers

Back to paper searchBrowse research topicsOriginal source
Specific c7c TNF-α mimotope phage clone as target for screening TNF-α specific binding-peptides from 12mer phage display peptide library — Research Paper | ScholarLens