The Global Goal of the project is to develop a rapid, accurate, and inexpensive diagnostic immuno-optical biosensor for Factor V Leiden (FVL) diagnosis. FVL is the most common hereditary blood coagulation disorder, comprising 3 - 7 percent of the general population and 20-40 percent of individuals with thrombosis. The sensor will be composed of an array of two optical fibers, with each immobilized monoclonal antibodies against normal Factor V (FVN) or FVL. After FVN/FVL in the sample reacts with the corresponding antibodies, they will be probed with a fluorophore tagged another antibody to specifically quantify the amount of these two molecules in the sample. This sensor will diagnose the FVL with high specificity (vs. clotting assays), faster (vs. DNA analysis), and less expensive, and also provide the information on the degree of thrombophilia by having the amount of both FVN and FVL. This early diagnosis method prevents patients from having traumatic thromboembolic complications, by allowing them to receive immediate treatments, when needed.
The specific aims to initiate the research goal are:
Aim 1. Purification of FVL from homozygous FVL patients (months 0-2 4). FVL molecules will be purified from the plasma of homozygous FVL patients.
Aim 2. Identification and Production of Antibodies against FVN/FV L (months 4-12). Monoclonal antibodies against either FVN or FVL have been generated. The affinity to the native form of FVN or FVL will be identified. Hybridoma cells producing proper antibodies wiII be cultured in bioreactors and purified.
Aim 3. Development of Sensors for FVN and FVL (months 7-24). Protocols developed for the Protein C biosensor will be used to detect FVN and FVL on two individual fiber optic sensors and a prototype of dual sensor will be developed.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21EB003485-01
Application #
6759572
Study Section
Hemostasis and Thrombosis Study Section (HT)
Program Officer
Kelley, Christine A
Project Start
2004-03-01
Project End
2006-02-28
Budget Start
2004-03-01
Budget End
2005-02-28
Support Year
1
Fiscal Year
2004
Total Cost
$197,600
Indirect Cost
Name
University of Louisville
Department
Engineering (All Types)
Type
Schools of Engineering
DUNS #
057588857
City
Louisville
State
KY
Country
United States
Zip Code
40292
Kang, Kyung A; Ren, Yongjie; Sharma, Vivek R et al. (2009) Near real-time immuno-optical sensor for diagnosing single point mutation: a model system: sensor for factor V Leiden diagnosis. Biosens Bioelectron 24:2785-90
Ren, Yongjie; Rezania, Samin; Kang, Kyung A (2008) Biosensor for diagnosing Factor V Leiden, a single amino acid mutated abnormality of Factor V. Adv Exp Med Biol 614:245-52
Rezania, Samim; Kang, Kyung A (2008) Separation of Factor V Leiden molecule, a mutated form of Factor V, from plasma of homozygous patient. Adv Exp Med Biol 614:101-7