1hbb: Difference between revisions

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[[Image:1hbb.gif|left|200px]]<br />
[[Image:1hbb.gif|left|200px]]<br /><applet load="1hbb" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1hbb" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1hbb, resolution 1.9&Aring;" />
caption="1hbb, resolution 1.9&Aring;" />
'''HIGH-RESOLUTION X-RAY STUDY OF DEOXYHEMOGLOBIN ROTHSCHILD 37BETA TRP-> ARG: A MUTATION THAT CREATES AN INTERSUBUNIT CHLORIDE-BINDING SITE'''<br />
'''HIGH-RESOLUTION X-RAY STUDY OF DEOXYHEMOGLOBIN ROTHSCHILD 37BETA TRP-> ARG: A MUTATION THAT CREATES AN INTERSUBUNIT CHLORIDE-BINDING SITE'''<br />


==Overview==
==Overview==
The mutation site in hemoglobin Rothschild (37 beta Trp----Arg) is located, in the "hinge region" of the alpha 1 beta 2 interface, a region that is, critical for normal hemoglobin function. The mutation results in greatly, reduced cooperativity and an oxygen affinity similar to that of hemoglobin, A [Gacon, G., Belkhodja, O., Wajcman, H., &amp; Labie, D. (1977) FEBS Lett., 82, 243-246]. Crystal were grown under "low-salt" conditions [100 mM Cl-, in 10 mM phosphate buffer at pH 7.0 with poly(ethylene glycol) as a, precipitating agent]. The crystal structure of deoxyhemoglobin Rothschild, and the isomorphous crystal structure of deoxyhemoglobin A were refined at, resolutions of 2.0 and 1.9 A, respectively. The mutation-induced, structural changes were partitioned into components of (1) tetramer, rotation, (2) quaternary structure rearrangement, and (3) deformations of, tertiary structure. The quaternary change involves a 1 degree rotation of, the alpha subunit about the "switch region" of the alpha 1 beta 2, interface. The tertiary changes are confined to residues at the alpha 1, beta 2 interface, with the largest shifts (approximately 0.4 A) located, across the interface from the mutation site at the alpha subunit FG, corner-G helix boundary. Most surprising was the identification of a, mutation-generated anion-binding site in the alpha 1 beta 2 interface., Chloride binds at this site as a counterion for Arg 37 beta. The, requirement of a counterion implies that the solution properties of, hemoglobin Rothschild, in particular the dimer-tetramer equilibrium, should be very dependent upon the concentration and type of anions, present.
The mutation site in hemoglobin Rothschild (37 beta Trp----Arg) is located in the "hinge region" of the alpha 1 beta 2 interface, a region that is critical for normal hemoglobin function. The mutation results in greatly reduced cooperativity and an oxygen affinity similar to that of hemoglobin A [Gacon, G., Belkhodja, O., Wajcman, H., &amp; Labie, D. (1977) FEBS Lett. 82, 243-246]. Crystal were grown under "low-salt" conditions [100 mM Cl- in 10 mM phosphate buffer at pH 7.0 with poly(ethylene glycol) as a precipitating agent]. The crystal structure of deoxyhemoglobin Rothschild and the isomorphous crystal structure of deoxyhemoglobin A were refined at resolutions of 2.0 and 1.9 A, respectively. The mutation-induced structural changes were partitioned into components of (1) tetramer rotation, (2) quaternary structure rearrangement, and (3) deformations of tertiary structure. The quaternary change involves a 1 degree rotation of the alpha subunit about the "switch region" of the alpha 1 beta 2 interface. The tertiary changes are confined to residues at the alpha 1 beta 2 interface, with the largest shifts (approximately 0.4 A) located across the interface from the mutation site at the alpha subunit FG corner-G helix boundary. Most surprising was the identification of a mutation-generated anion-binding site in the alpha 1 beta 2 interface. Chloride binds at this site as a counterion for Arg 37 beta. The requirement of a counterion implies that the solution properties of hemoglobin Rothschild, in particular the dimer-tetramer equilibrium, should be very dependent upon the concentration and type of anions present.


==Disease==
==Disease==
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==About this Structure==
==About this Structure==
1HBB is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with HEM as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1HBB OCA].  
1HBB is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=HEM:'>HEM</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1HBB OCA].  


==Reference==
==Reference==
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[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Arnone, A.]]
[[Category: Arnone, A.]]
[[Category: Kavanaugh, J.S.]]
[[Category: Kavanaugh, J S.]]
[[Category: HEM]]
[[Category: HEM]]
[[Category: oxygen transport]]
[[Category: oxygen transport]]


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