南方医科大学学报 ›› 2004, Vol. 24 ›› Issue (03): 252-255.

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人端粒酶逆转录酶功能区表位的筛选与鉴定

苗佩宏1, 刘北一2, 郑山根2, 庞建新1, 徐江平1   

  1. 1. 第一军医大学药理学教研室, 广东, 广州510515;
    2. 第一军医大学免疫学教研室, 广东, 广州510515
  • 出版日期:2004-03-20 发布日期:2004-03-20
  • 基金资助:
    收稿日期:2004-1-7。
    基金项目:国家自然科学基金(30000208)
    作者简介:苗佩宏(1970- ),男,第一军医大学在读硕士研究生,电话:020-61648220,E-mail:miaoph@fimmu.com
    通讯作者:庞建新,E-mail:pjx@fimmu.com

Screening and identification of human telomerase reverse transcriptase epitopes from random phage display peptide library

MIAO Pei-hong1, LIU Bei-yi2, ZHENG Shan-gen2, PANG Jian-xin1, XU Jiang-ping1   

  1. 1. 第一军医大学药理学教研室, 广东, 广州510515;
    2. 第一军医大学免疫学教研室, 广东, 广州510515
  • Online:2004-03-20 Published:2004-03-20

摘要: 目的 筛选并鉴定人端粒酶逆转录酶(hTERT)功能区表位。方法 应用差减筛选法,以抗hTERT多克隆抗体为靶筛选噬菌体12肽库,通过夹心ELISA、抗hTERT多抗特异性阻断实验、竞争抑制实验鉴定阳性噬菌体克隆并测序。结果 经3轮筛选,从随机挑取的24个噬菌体克隆中有13个克隆特异地与抗hTERT多抗结合,而不与正常小鼠IgG结合,其中11个克隆的氨基酸序列富含组氨酸(最高达41.6%)及亲水氨基酸(最高达91.67%)。结论 得到11个序列不同的hTERT表位,为研制针对hTERT的小分子抑制剂提供了实验依据。

Abstract: Objective To identify and characterize the epitopes of human telomerase reverse transcriptase (hTERT). Methods A random phage displayed dodecapeptide library was screened with anti-hTERT antibody. The selected phage clones were identified by sandwich enzyme-linked immunosorbent assay, anti-hTERT antibody blocking assay and competitive inhibition assay. Results After 3 rounds of screening, 13 of 24 randomly selected phage clones were identified as positive clones that could specifically bind to anti-hTERT antibody but not to normal mouse IgG. Amino acid sequences deduced from DNA sequences showed 11 different sequences with high percentage of histone and hydrophilic amino acids. Conclusion Eleven epitopes have been obtained that can effectively mimic hTERT, which will be useful for the research of small-molecule inhibitor targeting at hTERT.

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