Screening, identification and significance of the phage-display random 7 amino acid peptide specific to the sera of patients with systemic lupus erythematosus
10.3760/cma.j.issn.0254-5101.2010.07.019
- VernacularTitle:系统性红斑狼疮患者血清特异性的噬菌体7肽的筛选、鉴定及其意义
- Author:
Yao WANG
;
Liju SU
;
Hui LI
;
Yanhong LIU
;
Aixia ZHAI
;
Wenping KAO
;
Jing WU
;
Wenhui LI
;
Yunlong HU
;
Zhaohua ZHONG
;
Fengmin ZHANG
- Publication Type:Journal Article
- Keywords:
Phage peptide library;
Systemic lupus erythematosus;
Sera
- From:
Chinese Journal of Microbiology and Immunology
2010;30(7):665-669
- CountryChina
- Language:Chinese
-
Abstract:
Objective To screen and identify the phage-display random 7 amino acid peptide specific to the systemic lupus erythematosus(SLE) and analyze its practical significance. Methods Using the phage random 7 peptide library screening, the SLE specific phage clones are obtained after binding with the mixture of sera from 30 SLE patients and 30 normal controls as ligand respectively. Then the Dot-ELISA is used to identify the SLE specific phage clones reactive to sera of the SLE patients and normal controls individually. Finally the identified phage-display random 7 amino acid peptides are sequenced and it's homology with the antigenic epitope of human being and other are also analyzed. Results Total 12 of the phage-display random 7 amino acid peptide are obtained by phage peptide library screening and the Dot-ELISA identification. Sequence analysis shows that the identified phage-display random 7 amino acid peptide epitope have homology with E. coli, Salmonella and human immunodeficiency virus, but not with that of human being. Conclusion SLE-specific peptides screened by phage random peptide library maybe used to diagnosis the SLE. Meanwhile, the antibodies in SLE patients which are combined with the Pathogen epitope, suggest that SLE maybe relate to pathogen infection.
