Structure Interaction and Mechanism in Sickle Hemoglobin

  • Briehl, Robin W. (PI)
  • Bookchin, Robert M. (CoPI)
  • Ferrone, Frank A. (CoPI)
  • Josephs, Robert (CoPI)
  • Manning, James M. (CoPI)
  • Briehl, Robin R.W (CoPI)
  • Briehl, Robin Walt (CoPI)

Project: Research project

Project Details


DESCRIPTION (provided by applicant): The overall aim of this highly cooperative project is to characterize basic pathogenic processes in sickle cell crises and disease in order to develop treatments and prevention. We focus on a primary event in crises, polymerization of deoxygenated hemoglobin S (HbS) into rod-like fibers which form a rigid gel that induces microvascular obstruction. We address four themes, each with a major pathogenic role. 1) The rigidity of HbS fibers. Gel rigidity depends on fiber rigidity and the number and character of non-covalent interfiber cross-links. We will extend our recent characterization of fibers to study of the full gel and measurement of interfiber cross-linking forces. Also, vibrational entropy has been shown to be important governing the solubility of HbS. Since this entropy correlates with flexibility, we will study the effect of mutations with known effects on solubility on vibrational entropy and fiber rigidity. 2) Kinetics, equilibria and structure. The nucleation dependent, cooperative, kinetics of polymerization kinetics are central in pathogenesis. We seek to ascertain if the first nucleations might occur on red cell membranes as well as homogeneously in bulk solution. We also aim to identify the molecular site of subsequent nucleations, known to occur on existing fibers and responsible for the exponential nature of polymerization progress. 3) Depolymerization. Having recently characterized aspects of the mechanisms of depolymerization, we postulate that it too is critical in pathogenesis. We seek a model for rates and mechanisms for application to depolymerization within the pulmonary capillaries and during resolution of crises. 4) The red cell. The deleterious effects of solid-like rheology and rapid kinetics operate through effects on the red cell. We will examine the role of the membrane in polymerization and the effects of polymerization on it. Our expertise includes structural methods (EM, microscopy of fibers and gels) as well as physical chemical methods, theoretical analyses and red cell studies.
Effective start/end date8/6/9712/31/08


  • National Heart, Lung, and Blood Institute: $1,934,745.00
  • National Heart, Lung, and Blood Institute: $1,943,663.00
  • National Heart, Lung, and Blood Institute: $1,878,683.00


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