Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014 Jun;11(3):303-13.
doi: 10.1586/14789450.2014.893830. Epub 2014 Apr 4.

Quantitative targeted proteomics for understanding the blood-brain barrier: towards pharmacoproteomics

Affiliations
Review

Quantitative targeted proteomics for understanding the blood-brain barrier: towards pharmacoproteomics

Sumio Ohtsuki et al. Expert Rev Proteomics. 2014 Jun.

Abstract

The blood-brain barrier (BBB) is formed by brain capillary endothelial cells linked together via complex tight junctions, and serves to prevent entry of drugs into the brain. Multiple transporters are expressed at the BBB, where they control exchange of materials between the circulating blood and brain interstitial fluid, thereby supporting and protecting the CNS. An understanding of the BBB is necessary for efficient development of CNS-acting drugs and to identify potential drug targets for treatment of CNS diseases. Quantitative targeted proteomics can provide detailed information on protein expression levels at the BBB. The present review highlights the latest applications of quantitative targeted proteomics in BBB research, specifically to evaluate species and in vivo-in vitro differences, and to reconstruct in vivo transport activity. Such a BBB quantitative proteomics approach can be considered as pharmacoproteomics.

Keywords: absolute quantification; blood–brain barrier; brain capillary endothelial cells; multiple reaction monitoring; pharmacoproteomics; quantitative targeted proteomics; transporter.

PubMed Disclaimer

Publication types

Substances

LinkOut - more resources