Chemiluminescent optical fiber immunosensor for detection of autoantibodies to ovarian and breast cancer-associated antigens

被引:39
作者
Salama, Orly
Herrmann, Sebastien
Tziknovsky, Alina
Piura, Benjamin
Meirovich, Michael
Trakht, Ilya
Reed, Brent
Lobel, Leslie I.
Marks, Robert S. [1 ]
机构
[1] Ben Gurion Univ Negev, Dept Biotechnol Engn, Natl Inst Biotechnol, IL-84105 Beer Sheva, Israel
[2] Ben Gurion Univ Negev, Dept Virol, Fac Hlth Sci, IL-84105 Beer Sheva, Israel
[3] Ben Gurion Univ Negev, Div Obstet & Gynecol, Fac Hlth Sci, Soroka Univ Hosp, Beer Sheva, Israel
[4] Columbia Univ, Dept Med, New York, NY 10032 USA
[5] Louisiana State Univ, Hlth Sci Ctr, Dept Biochem & Mol Biol, Shreveport, LA 71130 USA
[6] Ben Gurion Univ Negev, Ilse Katz Ctr Meso & Nanoscale Sci & Technol, IL-84105 Beer Sheva, Israel
关键词
optical fiber immunosensor; GIPC-1; chemiluminescence; ovarian and breast cancer; human monoclonal antibody; cancer-associated antigen;
D O I
10.1016/j.bios.2006.07.003
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We report herein the development of an optical fiber based chemiluminescent immunosensor for detection of the native autoimmune response to GIPC-1, a PDZ containing protein involved in regulation of G-protein signaling. The recombinant protein GIPC-1 was expressed in bacteria, purified, refolded and conjugated to the tip of an optical fiber. A human monoclonal 27.B1 IgM isolated from a breast cancer patient, which targets the GIPC-I protein, was used for calibration of the immunosensor and was detected down to a concentration of 30 pg/ml. We determined that the fiber-optic immunosensor had a detection limit 50 times lower than chemiluminescent ELISA, and approximately 500 times lower than colorimetric ELISA. In addition, sera from I I ovarian cancer patients, 22 breast cancer patients and asymptomatic controls were tested for the presence of IgM anti-GIPC-1 autoantibodies in their serum using the two methods. The immunosensor assay detected 54% and 77% GIPC-1 positive sera within ovarian and breast cancer patients, respectively, as compared to chemiluminescent ELISA, which only detected 18% and 27%, respectively. We envision that this immunosensor may serve as a diagnostic tool for screening women for ovarian and breast cancer at an early stage, thus increasing their chance of survival. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1508 / 1516
页数:9
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