中南大学学报(医学版)
中南大學學報(醫學版)
중남대학학보(의학판)
JOURNAL OF CENTRAL SOUTH UNIVERSITY (MEDICAL SCIENCES)
2010年
3期
236-240
,共5页
王敏%李先平%王庆林%汤兰桂
王敏%李先平%王慶林%湯蘭桂
왕민%리선평%왕경림%탕란계
噬菌体随机肽库%模拟表位%丙型肝炎病毒
噬菌體隨機肽庫%模擬錶位%丙型肝炎病毒
서균체수궤태고%모의표위%병형간염병독
phage displayed random peptide library%mimic epitope%hepatitis C virus
目的:用丙型肝炎患者血清中抗丙型肝炎病毒(HCV)抗体从噬菌体随机12肽库中筛选HCV抗原表位.方法:将丙型肝炎患者血清混合,提取纯化的IgG作为固相配基筛选噬菌体随机12肽库,按吸附-洗脱-扩增的淘洗过程进行3轮筛选,随机挑取噬菌体克隆用ELISA法检测其特异性,对4个克隆进行测序.并用ELISA法检测噬菌体克隆的诊断价值.结果:3轮筛选的投入产出比逐轮升高,回收率从(4.6×10~(-4))%增加到(5.3×10~(-2))%,具有良好的富集效果.对从第3轮洗脱物中挑选出的18个克隆进行结合试验,发现所挑的克隆与丙型肝炎患者的多克隆抗体有较强的结合力.其中4个克隆测序显示为同一克隆(命名为C1),其外源插入肽为GSMSPYVRWYTP.用C1检测20例丙型肝炎患者血清的检出率为85.0%.结论:成功地用噬菌体12肽库对丙型肝炎患者血清进行了模拟肽筛选,且得到的模拟肽分子C1具有一定的诊断价值.
目的:用丙型肝炎患者血清中抗丙型肝炎病毒(HCV)抗體從噬菌體隨機12肽庫中篩選HCV抗原錶位.方法:將丙型肝炎患者血清混閤,提取純化的IgG作為固相配基篩選噬菌體隨機12肽庫,按吸附-洗脫-擴增的淘洗過程進行3輪篩選,隨機挑取噬菌體剋隆用ELISA法檢測其特異性,對4箇剋隆進行測序.併用ELISA法檢測噬菌體剋隆的診斷價值.結果:3輪篩選的投入產齣比逐輪升高,迴收率從(4.6×10~(-4))%增加到(5.3×10~(-2))%,具有良好的富集效果.對從第3輪洗脫物中挑選齣的18箇剋隆進行結閤試驗,髮現所挑的剋隆與丙型肝炎患者的多剋隆抗體有較彊的結閤力.其中4箇剋隆測序顯示為同一剋隆(命名為C1),其外源插入肽為GSMSPYVRWYTP.用C1檢測20例丙型肝炎患者血清的檢齣率為85.0%.結論:成功地用噬菌體12肽庫對丙型肝炎患者血清進行瞭模擬肽篩選,且得到的模擬肽分子C1具有一定的診斷價值.
목적:용병형간염환자혈청중항병형간염병독(HCV)항체종서균체수궤12태고중사선HCV항원표위.방법:장병형간염환자혈청혼합,제취순화적IgG작위고상배기사선서균체수궤12태고,안흡부-세탈-확증적도세과정진행3륜사선,수궤도취서균체극륭용ELISA법검측기특이성,대4개극륭진행측서.병용ELISA법검측서균체극륭적진단개치.결과:3륜사선적투입산출비축륜승고,회수솔종(4.6×10~(-4))%증가도(5.3×10~(-2))%,구유량호적부집효과.대종제3륜세탈물중도선출적18개극륭진행결합시험,발현소도적극륭여병형간염환자적다극륭항체유교강적결합력.기중4개극륭측서현시위동일극륭(명명위C1),기외원삽입태위GSMSPYVRWYTP.용C1검측20례병형간염환자혈청적검출솔위85.0%.결론:성공지용서균체12태고대병형간염환자혈청진행료모의태사선,차득도적모의태분자C1구유일정적진단개치.
Objective To analyze the epitopes of anti-hepatitis C virus(HCV)antibodies by peptide library biopanning. Methods Phage random peptide library of 12 amino acids was immunoscreened with purified IgG from the sera of hepatitis C patients. Positive clones which were obtained after 3 rounds of biopanning were detected by ELISA and 4 of them were sequenced. Results After 3 rounds of screening, the radio of output to input increased from (4.6×10~(-4))% to (5.3×10~(-2))%, meaning the enrichment was effective. At the third round of screening, all the selected clones proved to specifically react with the sera for immunoscreening. Four positive phage clones were sequenced, which shared a very conservative sequence and was named as C1. Its inserting sequence in the coat protein III was deduced to be GSMSPYVRWYTP, and the positive rate of C1 reacted with 20 cases of HCV patients was 85%.Conclusion The antigen-mimic peptide C1 is successfully screened from 12 random phage peptide library and it has some diagnostic value.