Journal
BIOPHYSICAL JOURNAL
Volume 87, Issue 4, Pages 2621-2629Publisher
CELL PRESS
DOI: 10.1529/biophysj.104.039743
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Funding
- NHLBI NIH HHS [HL3865, F31 HL009564, HL58038, 1F31HL09564-01] Funding Source: Medline
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Crystallization of the mutated hemoglobin, HbC, which occurs inside red blood cells of patients expressing beta(C)-globin and exhibiting the homozygous CC and the heterozygous SC (in which two mutant beta-globins, S and C, are expressed) diseases, is a convenient model for processes underlying numerous condensation diseases. As a first step, we investigated the molecular-level mechanisms of crystallization of this protein from high-concentration phosphate buffer in its stable carbomonoxy form using high-resolution atomic force microscopy. We found that in conditions of equilibrium with the solution, the crystals' surface reconstructs into four-molecule-wide strands along the crystallographic a (or b) axis. However, the crystals do not grow by the alignment of such preformed strands. We found that the crystals grow by the attachment of single molecules to suitable sites on the surface. These sites are located along the edges of new layers generated by two-dimensional nucleation or by screw dislocations. During growth, the steps propagate with random velocities, with the mean being an increasing function of the crystallization driving force. These results show that the crystallization mechanisms of HbC are similar to those found for other proteins. Therefore, strategies developed to control protein crystallization in vitro may be applicable to pathology-related crystallization systems.
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