Studies on the mode of action of two antisickling agents, glyceraldehyde and methyl acetyl phosphate, will be continued from three perspectives. Studies aimed at the chemical mechanism of the reaction of each of these compounds with hemoglobin S will be pursued. With glyceraldehyde we are especially interested in uncovering the mechanism of the Amadori rearrangement. For this purpose we will be studying model peptide systems in which we have already separated the intermediate aldimine and product ketoamine by mild chromatographic procedures. The stability of each of these adducts will be evaluated under a variety of conditions. For methyl acetyl phosphate we will continue to study the reason for the lowered oxygen affinity when this acetylating agent reacts with hemoglobin S in the deoxy state. Studies on cell density and oxygen affinity will also be performed. The second part of these studies will evaluate the effects of each of these compounds on intact sickled cells. This is made possible because each compound can readily enter the sickle cell and react with intracellular hemoglobin. We plan to study the kinetics of deformability of the sickle cell after treatment with either glyceraldehyde or methyl acetyl phosphate. Studies on cell density using the phthalate ester method will also be performed, as well as studies on the viscosity of suspensions of sickled cells. Studies on hemoglobin biosynthesis in a reticulocyte system will be performed in the presence of glyceraldehyde or methyl acetyl phosphate. The third aspect of these studies will involve preclinical studies. For either glyceraldehyde or methyl acetyl phosphate, studies in animals will be carried out to determine how much of a given dose administered by various routes will be necessary to achieve the desirable amount of reaction with circulating red cells in vivo. In humans, studies on glyceraldehyde will be pursued in order to determine whether or not there is any new immunological determinant which is conferred upon the cells after the treatment with glyceraldehyde. For these purposes we will perform Coombs tests as well as a third chromate survival time in vivo. Finally, we will continue to assist Dr. Samuel Charache of Johns Hopkins in his studies on the treatment of sickle cells with glyceraldehyde.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37HL018819-19
Application #
3485589
Study Section
Virology Study Section (VR)
Project Start
1982-07-01
Project End
1992-06-30
Budget Start
1990-07-01
Budget End
1991-06-30
Support Year
19
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Rockefeller University
Department
Type
Other Domestic Higher Education
DUNS #
071037113
City
New York
State
NY
Country
United States
Zip Code
10065
Manning, Lois R; Popowicz, Anthony M; Padovan, Julio et al. (2010) Developmental expression of human hemoglobins mediated by maturation of their subunit interfaces. Protein Sci 19:1595-9
Manning, Lois R; Russell, J Eric; Popowicz, Anthony M et al. (2009) Energetic differences at the subunit interfaces of normal human hemoglobins correlate with their developmental profile. Biochemistry 48:7568-74
Manning, Lois R; Russell, J Eric; Padovan, Julio C et al. (2007) Human embryonic, fetal, and adult hemoglobins have different subunit interface strengths. Correlation with lifespan in the red cell. Protein Sci 16:1641-58
Ashiuchi, Makoto; Yagami, Takeshi; Willey, Ronald J et al. (2005) N-terminal acetylation and protonation of individual hemoglobin subunits: position-dependent effects on tetramer strength and cooperativity. Protein Sci 14:1458-71
Geva, Alon; Clark, Jennifer J; Zhang, Yuxun et al. (2004) Hemoglobin Jamaica plain--a sickling hemoglobin with reduced oxygen affinity. N Engl J Med 351:1532-8
Zhang, Yuxun; Manning, Lois R; Falcone, Jill et al. (2003) Human erythrocyte membrane band 3 protein influences hemoglobin cooperativity. Possible effect on oxygen transport. J Biol Chem 278:39565-71
Manning, L R; Manning, J M (2001) The acetylation state of human fetal hemoglobin modulates the strength of its subunit interactions: long-range effects and implications for histone interactions in the nucleosome. Biochemistry 40:1635-9
Chen, W; Dumoulin, A; Li, X et al. (2000) Transposing sequences between fetal and adult hemoglobins indicates which subunits and regulatory molecule interfaces are functionally related. Biochemistry 39:3774-81
Li, X; Himanen, J P; Martin de Llano, J J et al. (1999) Mutational analysis of sickle haemoglobin (Hb) gelation. Biotechnol Appl Biochem 29 ( Pt 2):165-84
Manning, J M; Dumoulin, A; Manning, L R et al. (1999) Remote contributions to subunit interactions: lessons from adult and fetal hemoglobins. Trends Biochem Sci 24:211-2

Showing the most recent 10 out of 53 publications