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Heavy chain single-domain antibodies to detect native human soluble epoxide hydrolase.

Authors :
Cui Y
Li D
Morisseau C
Dong JX
Yang J
Wan D
Rossotti MA
Gee SJ
González-Sapienza GG
Hammock BD
Source :
Analytical and bioanalytical chemistry [Anal Bioanal Chem] 2015 Sep; Vol. 407 (24), pp. 7275-83. Date of Electronic Publication: 2015 Jul 31.
Publication Year :
2015

Abstract

The soluble epoxide hydrolase (sEH) is a potential pharmacological target for treating hypertension, vascular inflammation, pain, cancer, and other diseases. However, there is not a simple, inexpensive, and reliable method to estimate levels of active sEH in tissues. Toward developing such an assay, a polyclonal variable domain of heavy chain antibody (VHH) sandwich immunoassay was developed. Ten VHHs, which are highly selective for native human sEH, were isolated from a phage-displayed library. The ten VHHs have no significant cross-reactivity with human microsomal epoxide hydrolase, rat and mouse sEH, and denatured human sEH. There is a high correlation between protein levels of the sEH determined by the enzyme-linked immunosorbent assay (ELISA) and the catalytic activity of the enzyme in S9 fractions of human tissues (liver, kidney, and lung). The VHH-based ELISA appears to be a new reliable method for monitoring the sEH and may be useful as a diagnostic tool for diseases influenced by sEH. This study also demonstrates the broad utility of VHH in biochemical and pharmacological research.

Details

Language :
English
ISSN :
1618-2650
Volume :
407
Issue :
24
Database :
MEDLINE
Journal :
Analytical and bioanalytical chemistry
Publication Type :
Academic Journal
Accession number :
26229025
Full Text :
https://doi.org/10.1007/s00216-015-8889-6