Having solved the phase problem at 3.3A resolution for the octameric histone core of the nucleosome by iterated single isomorphous replacement with solvent flattening and anomolous dispersion, it is proposed to fit the amino acid sequences to the electron density map and extend the resolution of 2.8A. Having solved the phase problem for the carbon omonoxide complex of both the dimeric and tetrameric hemoglobins of the blood claim Scafarca inaequivalvis by a combination of multiple heavy atom isomorphous replacement, symmetry averaging and molecular replacement, it is proposed to fit the amino acid sequences to the electron density maps and extend the resolution to at least 2.0A. It is also proposed to prepare crystals of the dimeric and tetrameric deoxy clam hemoglobins and to determine their structures so that the structural alterations accompanying cooperative ligand binding can be seen. It is proposed to refine the structures of deoxy and carbon monoxide Glycera hemoglobin at 1.5A resolution in order to define the structural alterations that accompany ligand binding in a monomeric hemoglobin lacking a distal histidine.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK002528-31
Application #
3224364
Study Section
Biophysical Chemistry Study Section (BBCB)
Project Start
1977-09-01
Project End
1992-03-31
Budget Start
1990-04-01
Budget End
1992-03-31
Support Year
31
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
Schools of Arts and Sciences
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Braden, B C; Arents, G; Padlan, E A et al. (1994) Glycera dibranchiata hemoglobin. X-ray structure of carbonmonoxide hemoglobin at 1.5 A resolution. J Mol Biol 238:42-53
Arents, G; Love, W E (1989) Glycera dibranchiata hemoglobin. Structure and refinement at 1.5 A resolution. J Mol Biol 210:149-61