A phage-displayed single chain variable fragment that interacts with hepatitis B core antigen: Library construction, selection and diagnosis

被引:5
|
作者
Tan, Geok Hun
Yusoff, Khatijah
Seow, Heng Fong
Tan, Wen Siang
机构
[1] Univ Putra Malaysia, Fac Biotechnol & Biomol Sci, Dept Microbiol, Serdang 43400, Selangor, Malaysia
[2] Univ Putra Malaysia, Inst Biosci, Serdang 43400, Selangor, Malaysia
[3] Univ Putra Malaysia, Fac Med & Hlth Sci, Dept Clin Lab Sci, Serdang 43400, Selangor, Malaysia
关键词
phage display; combinatorial antibody libraries; hepatitis B core antigen; diagnosis; phage-ELISA;
D O I
10.1016/j.jcv.2006.09.010
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Phage display is an alternative method for constructing and selecting antibodies with desired specificity towards an antigen. Objectives: To construct a library of single chain variable fragment (ScFv) towards hepatitis B core antigen (HBcAg). To isolate a ScFv phage clone that interacts with HBcAg and to develop a phage-ELISA for detecting the antigen. Study design: Mice were inoculated with HBcAg and RNA was extracted from their spleen cells. The genes encoding heavy (V-H) and light (V-L) chains were amplified, linked via PCR and cloned into a phagemid vector. Phage particles displaying ScFv were panned against HBcAg and a selected clone was characterized and employed as a diagnostic reagent for detecting HBcAg in serum samples. Results: A phage clone that interacts with HBcAg was selected from the antibody library. The binding of the phage to HBcAg was inhibited by a cyclic peptide bearing the WSFFSNI sequence. A phage-ELISA was established using the recombinant phage and as low as 10 ng of HBcAg can be detected by the assay. Conclusion: The ScFv displayed on the surface of filamentous phage is an alternative choice for diagnosis of HBcAg in serum samples. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:49 / 56
页数:8
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