期刊文献+

人源性抗乳腺癌单链抗体库的筛选与初步鉴定 被引量:4

Isolation and identification of single chain Fv antibodies against breast cancer from a human phage display library
下载PDF
导出
摘要 目的:本研究旨在已构建的大容量人源性抗乳腺癌噬菌体单链抗体库的基础上,筛选出高亲和力的特异性单链抗体(scFv)并对抗体基本特性进行初步鉴定。方法:以人乳腺癌细胞系MCF-7为靶标,经过4轮淘洗,筛选出高亲和力的特异性抗乳腺癌scFv,并对其结构序列进行分析;通过ELISA和Western blot方法,鉴定scFv的亲和力和特异性,以及其蛋白的基本表达情况。结果:成功构建具有高亲和力的抗乳腺癌单链抗体库,获得scFv的长度约为750 bp,ELISA证实所得抗体对乳腺癌细胞具有良好的亲和力和高度的特异性,IPTG诱导表达及Western blot结果显示,scFv为相对分子质量(Mr)30 000的可溶性蛋白。结论:本研究在已构建的大容量抗乳腺癌单链抗体库的基础上,筛选获得了高亲和力的抗乳腺癌单链抗体库。研究结果为进一步获得可应用于临床诊断和治疗的乳腺癌靶向性抗体奠定了良好的基础。 AIM: To isolate and identify single chain Fv(scFv) antibodies against breast cancer from a constructed human phage display library.METHODS: Recombinant phages specific for breast cancer cells were enriched after four-round screening with MCF-7 cells.We selected the antigen-positive ones from the enriched clones by phage ELISA.The positive clones were used to infect E.coli HB2151 to express soluble scFv antibody.The antigen binding activity of the soluble antibodies was detected by Western blotting.RESULTS: The specific antibodies against MCF-7 cells were enriched after four rounds of affinity selection.SDS-PAGE and Western blotting showed a band at relative molecular mass 30 000 Da,which indicated soluble antibodies were present.ELISA analysis revealed that soluble antibodies had the affinity to a human breast cancer cell line MCF-7 but not to other cancer cell line,which demonstrated scFv could react specifically with breast cancer cells.CONCLUSION: We constructed a scFv phage library against human breast cancer with high capacity by phage display technology.The scfv was demonstrated successfully to be expressed in E.coli HB215 and have a specificity to breast cancer.Our findings may provide an alternative approach,and a basis for further studies on diagnosis and therapy of breast cancer.
出处 《细胞与分子免疫学杂志》 CAS CSCD 北大核心 2012年第8期837-840,共4页 Chinese Journal of Cellular and Molecular Immunology
基金 国家自然科学基金(81070249) 国家"重大新药创制"科技重大专项(2009ZX09102-226)
关键词 单链抗体 乳腺癌 人源性 噬菌体抗体库 筛选 表达 scFv breast cancer(mastocarcinoma) human phage display antibody library screen expression
  • 相关文献

参考文献3

  • 1Yokota T, Milenic DE, Whitlow M, et al. Rapid tumor penetration of a single-chain Fv and comparison with other immunoglobulin forms [J]. Cancer Res, 1992, 52(12) : 3402 -3408.
  • 2王净,王慧,袁媛,李青.全人源抗乳腺癌噬菌体单链抗体库的构建[J].现代肿瘤医学,2011,19(11):2139-2142. 被引量:2
  • 3Valabrega G, Montemurro F, Aglietta M. Trastuzumab: mechanism of action, resistance and future perspectives in HER2-overexpressing breast cancer[J]. Ann Oncol, 2007, 18(6) : 977 -984.

二级参考文献18

  • 1唐晓明,王清明,杨俊涛,陈吉中,范国才,汪思应.大容量人天然抗体库的构建、鉴定及初步应用[J].中国生物工程杂志,2005,25(10):17-24. 被引量:4
  • 2Carter P, Presta L, Gorman CM, et al. Humanization of an anti p185HER2 antibody for human cancer therapy [ J ]. Proc Nail Acad Sei USA,1992,89:4285 -4289.
  • 3Mc Cafferty J, Criffiths AD, Winter G, et al. Phage antibody: filamentous phage displaying antibody variable domains [ J ]. Nature, 1990:348:552-554.
  • 4Clackson T, Hoogenboom HR, Griffiths AD, et al. Making antibody fragments using phage display libraries [ J ]. Nature, 1991,352 (15) :624 -628.
  • 5Hoogenboom HR, Chames P. Natural and designer binding sites made by phage display technology[J]. Immunol Today,2000,21 : 371-378.
  • 6Winter G, Griffiths AD, Hawkins RE. Making antibodies by phage display technology[ J]. Annu Rev Immunol, 1994,12:433-455.
  • 7Sblattero D, Bradbury A. A definitive set of oligonueleotide primers for amplifying human V regions [ J ]. Immunoteehnology, 1998,3 (4) :271 -278.
  • 8Marks JD,Tristem M, Karpas A. Oligonucleotide primers for polymerase chain reaction amplification of human immunoglobulin variable genes and design of family-specific oligonucleotide probes [J]. Eur J Immunol,1991,21 (4) :985 -991.
  • 9Olandi R, Gussow D, Jones PT et al. Cloning immunoglobulin variable domains for expression by the polymerase chain reaction [ J]. Proc Natl Acad Sci USA, 1989,86:3833-3837.
  • 10Philippa M. OBrien,Robert Aitken,et al. Antibody phage display [J]. Methods and Protocols,2010,91 -93.

共引文献1

同被引文献38

引证文献4

二级引证文献10

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部