| Literature DB >> 26229025 |
Yongliang Cui1,2, Dongyang Li1,3,2, Christophe Morisseau1,2, Jie-Xian Dong1,2, Jun Yang1,2, Debin Wan1,2, Martín A Rossotti4, Shirley J Gee1,2, Gualberto G González-Sapienza4, Bruce D Hammock5,6.
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.Entities:
Keywords: ELISA; Magnetic beads; Soluble epoxide hydrolase; VHH; sEH
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Year: 2015 PMID: 26229025 PMCID: PMC4573264 DOI: 10.1007/s00216-015-8889-6
Source DB: PubMed Journal: Anal Bioanal Chem ISSN: 1618-2642 Impact factor: 4.142