Text Size Normal Text Sizing Button Medium Text Sizing Button Large Text Sizing Button Text Contrast Normal Contrast Button Reverse Contrast Button Switch to Spanish Language Contact Us Sitemap Sign In Register
Link to Homepage About AHAF
Donate Now Get Involved  
Alzheimer's Disease Research Macular Degeneration Research National Glaucoma Research


Sign up for Email Notifications
If you would like to be notified when submission deadlines are announced please click on the appropriate link below.

Alzheimer's Disease Research
Macular Degeneration Research
National Glaucoma Research

This email list is not sold or distributed, and serves only as an annual reminder of the availability of research funding through the American Health Assistance Foundation (www.ahaf.org). Please follow instructions on the notification emails for removal requests.

 
AHAF Research Grants Funding
Grant Funding for Alzheimer's Research
Grant Funding for Macular Degeneration Research
Grant Funding for Glaucoma Research
 

 

Macular Degeneration Research - Completed Award

Photo Pending

Qiuyun Chen, Ph.D.

The Cleveland Clinic Foundation
Cleveland, OH

Title: Identification of Human Retinal Lutein Binding Proteins
Non-Technical Title: Determining ways to modulate lutein levels in the eye

Duration: April 1, 2006 - March 31, 2009
Award Type: Standard
Award Amount: $200,000


Summary:

These investigators will identify lutein binding proteins from human retina by searching for genes that when expressed will produce proteins that specifically bind lutein. Once the gene(s) are identified, we will determine what type of proteins they are and whether their distribution in the retina correlates with the lutein distribution pattern.

Details:

The long-term goal of this project is to study the molecular basis for therapeutic manipulation of lutein levels in the retina in order to treat age-related macular degeneration (AMD) , the leading cause of incurable blindness in the western world. Lutein is one of the few carotenoids that are selectively accumulated in the human macula. Low concentrations of lutein in the retina have been found to correlate with a high risk of developing AMD. However, the exact molecular mechanisms underlying the protective function of carotenoids are unresolved. One reason this problem persists is the lack of knowledge of how and why lutein is selectively accumulated in the macula. Our hypothesis is that specific binding proteins facilitate the transport and retention of lutein in the retina. To test this hypothesis, we will identify lutein binding proteins from human retina by searching for genes that when expressing will produce proteins that specifically bind lutein. Once the gene(s) are identified, we will determine what type of proteins they are and whether their distribution in the retina correlates with the lutein distribution pattern.