Smokers are well known to be at elevated risk of cardiovascular disease and thrombosis. Thrombomodulin is a key regulator of blood clotting. Oxidation of methionine 388 in thrombomodulin greatly slows the rate at which the thrombomodulin-thrombin complex activates protein C, which, upon activation, slows clot formation. Smoking is known to impose an oxidative stress on the body. The hypothesis to be further confirmed is that oxidation of this methionine in thrombomodulin is elevated in smokers relative to non-smokers. Work will be done to improve the process of isolating thrombomodulin from urine. Further development of chromatographic methods using a new chromatographic system in order to improve chromatographic resolution and signal to noise ratios will also be undertaken. These improved methods will be used to test the oxidation levels of more smokers and non-smokers.

Public Health Relevance

We are working to determine the extent to which a protein, thrombomodulin, which regulates blood clotting, is more modified in smokers than non-smokers. The leading cause of premature death in smokers is heart disease, and this may be related to the fact that the blood of smokers is more prone to clot than non- smokers perhaps partly because of greater modification of this protein in smokers.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
2R15HL078994-02A1
Application #
7646658
Study Section
Hemostasis and Thrombosis Study Section (HT)
Program Officer
Sarkar, Rita
Project Start
2005-01-01
Project End
2011-03-31
Budget Start
2009-04-01
Budget End
2011-03-31
Support Year
2
Fiscal Year
2009
Total Cost
$176,378
Indirect Cost
Name
University of Arkansas at Fayetteville
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
191429745
City
Fayetteville
State
AR
Country
United States
Zip Code
72701
Saunders, Christopher C; Stites, Wesley E (2012) An electrophoretic mobility shift assay for methionine sulfoxide in proteins. Anal Biochem 421:767-9
Ross, Christopher C; MacLeod, Stewart L; Plaxco, Jason R et al. (2008) Inactivation of thrombomodulin by ionizing radiation in a cell-free system: possible implications for radiation responses in vascular endothelium. Radiat Res 169:408-16
Stites, Wesley E; Froude 2nd, Jeffrey W (2007) Does the oxidation of methionine in thrombomodulin contribute to the hypercoaguable state of smokers and diabetics? Med Hypotheses 68:811-21