期刊文献+

噬菌体展示蛋白质芯片的无标记检测

Label-free detection of phage-displayed protein chips
原文传递
导出
摘要 为获得丰富的特异识别分子和实现无标记、高灵敏度检测,利用噬菌体展示技术,选择在pIII蛋白上展示12肽的噬菌体M13作探针,采用羧基-氨基共价耦联法制备噬菌体展示蛋白质芯片。在此基础上,与表面等离子体共振传感技术结合,使用Biacore3000仪器,检测噬菌体展示蛋白质芯片与特异性抗体的反应,测定反应动力学常数。实验结果表明:当抗体浓度为0.4μmol.L-1时,响应信号可达365±8个单位;不同浓度的抗体与芯片反应的数据较好地与S型曲线吻合。该方法可望用于噬菌体展示蛋白质芯片的检测。 Surface plasmon resonance and the phage display technique were combined to enable use of a variety of specific reagents for label-flee, high sensitivity detection in protein chips. Phage M13 which displays 12 peptides on its coated protein plII was selected as the probe to prepare the phage-displayed protein chip using the amine coupling method. The specific interactions between the chip and the antibodies were detected using Biacore3000, with the binding kinetic parameters determined. Tests show that an antibody concentration of 0. 4μmol .L-1 gives response units of 365 :k 8, and that the relationship between the binding responses and the various antibody concentrations is well fit by the sigrnoid curve. The method can be used to optimize the detecting conditions for phage-displayed protein chips.
出处 《清华大学学报(自然科学版)》 EI CAS CSCD 北大核心 2008年第11期1935-1939,共5页 Journal of Tsinghua University(Science and Technology)
基金 国家自然科学基金资助项目(30727001) 高等学校博士学科点专项科研基金资助项目(20050003056)
关键词 表面等离子体共振 噬菌体M13展示系统 噬菌体展示蛋白质芯片 特异性抗体 动力学常数 surface plasmon resonance phage M13 display system phage-displayed protein chip specific antibody kinetic parameter
  • 相关文献

参考文献10

  • 1Pandey A, Mann M. Proteomics to study genes and genomes [J]. Nature, 2000, 405: 837- 746.
  • 2Zhu H, Suyder M. Protein chip technology [J]. Current Opinion in Chemical Biology, 2003, 7: 55- 63.
  • 3Silacci M, Brack S, Schirru G, et al. Design, construction, and characterization of a large synthetic human antibody phage display library [J]. Proteomics, 2005, 5: 2340-2350.
  • 4Hust M, DuLacl S. Mating antibody phage display with proteomics [J]. Trends in Biotechnology, 2004, 22(1): 8-14.
  • 5McCafferty J, Griffiths A D, Winter G, et al. Phage antibodies: Filamentous phage display antibody variable domains [J]. Nature, 1990, 348: 552-554.
  • 6Homola J. Present and future of surface plasmon resonance biosensors [J]. Anal Bioanal Chem, 2003, 377: 528- 539.
  • 7Balasubramanian S, SorokμLova I B, Vodyanoy V J, et al. Lytic phage as a specific and selective probe for detection of Staphylococcusaureus--A surface plasmon resonance spectroscopic study [J]. Biosensors and Bioelectronlcs, 2007, 22:948 - 955.
  • 8Nanduri V, Bhunia A K, Tu S, et al. SPR biosensor for the detection of L. monocytogenes using phage-displayed antibody [J]. Biosensors and Bioelectronics, 2007, 23:248 - 252.
  • 9Campbell C T, Kim G. SPR microscopy and its applications to high-throughput analyses of biomolecular binding events and their kinetics [J]. Biomaterials, 2007, 28: 2380-2392.
  • 10Green R J, Frazier R A, Shakeshe K M, et al. Surface plasmon resonance analysis of dynamic biological interactions with biomaterials [J]. Biomaterials, 2000, 21: 1823-1835.

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