This project proposes to answer question about the molecular basis of the pathology engendered by HbC and its effect on double heterozygotes for HbC and HbS. The first fundamental question is: what is the molecular basis of the tendency of oxyHb to crystallize? The present data points to the combination of the presence of the Beta6lysine mutation and alteration of the central cavity of the BetaA helix moving away from the heme as the best candidates. With state-of-the- art spectroscopy and X-ray crystallography the investigators propose to prove or disprove this hypothesis. The next fundamental question is: are these modulators in red cells that favor or inhibit crystallization, but the question remains whether or not other components of the cytosol are participants. To answer this question the investigators need to know more about crystal growth and more about the presence or absence of coring in these crystals. The investigators have joined forces with Rosenberger and Vekilov (Center for Microgravity and Materials Research, University of Alabama) to answer this question, using cutting-age custom made instrumentation to follow crystal growth and coring (coring is the presence of """"""""impurities that accelerate or retard crystal growth). Finally, another fundamental question is the molecular basis of the uniform microcytosis which varies among the syndromes containing HbC. One possibility is that this effect is related to abnormal interaction of HbC with the membrane specifically affecting volume-regulating transporters. Hence, the investigators need to test if the abnormal turn-off of K:C1 co- transport, discover by the group in C cells, is the culprit. For this purpose the investigators are in the process of generating transgenic mice expressing HbC and transgenic mice expressing the human K:C1 co- transporter (since the mouse K:C1 co-transporter has phenomenological differences with the human transporter). The potential answers to the above questions have practical applications: since SC disease is caused by an increase in intracellular HB concentration induced by HbC in RBC containing only 50 percent of Hbs, the investigations could cure this disease by correcting the transport abnormality. Also, since crystallization of HbC has polymerization in SC cells, the severity of the syndrome will be reduced significantly.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Comprehensive Center (P60)
Project #
5P60HL038655-15
Application #
6593857
Study Section
Project Start
2002-05-20
Project End
2003-03-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
15
Fiscal Year
2002
Total Cost
$175,153
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Type
DUNS #
009095365
City
Bronx
State
NY
Country
United States
Zip Code
10461
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