4.7 Article

Open-sandwich immunoassay for sensitive and broad-range detection of a shellfish toxin gonyautoxin

Journal

ANALYTICA CHIMICA ACTA
Volume 793, Issue -, Pages 107-113

Publisher

ELSEVIER
DOI: 10.1016/j.aca.2013.07.024

Keywords

Open sandwich immunoassay; Gonyautoxin; PSP toxins; Phage display; Maltose binding protein; Hapten

Funding

  1. MEXT, Japan [B24360336]
  2. Fujifilm. Co. Ltd.
  3. Grants-in-Aid for Scientific Research [25630370] Funding Source: KAKEN

Ask authors/readers for more resources

At present, the analytical method for paralytic shellfish poisoning (PSP) toxins in shellfish is the mouse bioassay (MBA), which is an official method of the Association of Analytical Communities (AOAC [8]). However, the low sensitivity and concerns over the number of live animals required for testing have been cited as the major reason for seeking its replacement. In this report, we employed an open-sandwich immunoassay (OS-IA) to detect gonyautoxin (GTX2/3), a kind of PSP toxins. OS-IA, which utilizes the antigen-induced enhancement of antibody V-H/V-L interaction, can measure a small molecule antigen in a noncompetitive format. Hence it has a wider working range and shorter measurement time. We isolated anti-GTX2/3 antibody gene from a hybridoma GT-13A by screening a Fab-displaying phage library. Then the vectors for OS-IA were constructed, and examined for antigen concentration-dependency of the V-H/V-L interaction by OS-ELISA. As a result, in each case, signal intensity increases notably in a wide concentration range (0.1 to >1000 ng mL(-1)) of free GTX2/3, which was enough to cover its regulation value (80 mu g 100 g(-1)) in many countries. So OS-IA will be widely applicable to detect PSP toxins in shellfish meats and in drinking water. (C) 2013 Elsevier B.V. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available