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


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.

SUBMITTER: Cui Y 

PROVIDER: S-EPMC4573264 | biostudies-literature | 2015 Sep

REPOSITORIES: biostudies-literature

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

Cui Yongliang Y   Li Dongyang D   Morisseau Christophe C   Dong Jie-Xian JX   Yang Jun J   Wan Debin D   Rossotti Martín A MA   Gee Shirley J SJ   González-Sapienza Gualberto G GG   Hammock Bruce D BD  

Analytical and bioanalytical chemistry 20150731 24


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.  ...[more]

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