1orm: Difference between revisions

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[[Image:1orm.jpg|left|200px]]<br /><applet load="1orm" size="~~450~~" color="white" frame="true" align="right" spinBox="true"

[[Image:1orm.jpg|left|200px]]<br /><applet load="1orm" size="350" color="white" frame="true" align="right" spinBox="true"

caption="1orm" />

'''NMR FOLD OF THE OUTER MEMBRANE PROTEIN OMPX IN DHPC MICELLES'''<br />

==Overview==

The (2)H,(13)C,(15)N-labeled, 148-residue integral membrane protein OmpX, from Escherichia coli was reconstituted with dihexanoyl, phosphatidylcholine (DHPC) in mixed micelles of molecular mass of about 60, kDa. Transverse relaxation-optimized spectroscopy (TROSY)-type triple, resonance NMR experiments and TROSY-type nuclear Overhauser enhancement, spectra were recorded in 2 mM aqueous solutions of these mixed micelles at, pH 6.8 and 30 degrees C. Complete sequence-specific NMR assignments for, the polypeptide backbone thus have been obtained. The (13)C chemical, shifts and the nuclear Overhauser effect data then resulted in the, identification of the regular secondary structure elements of OmpX/DHPC in, solution and in the collection of an input of conformational constraints, for the computation of the global fold of the protein. The same type of, polypeptide backbone fold is observed in the presently determined solution, structure and the previously reported crystal structure of OmpX determined, in the presence of the detergent n-octyltetraoxyethylene. Further, structure refinement will have to rely on the additional resonance, assignment of partially or fully protonated amino acid side chains, but, the present data already demonstrate that relaxation-optimized NMR, techniques open novel avenues for studies of structure and function of, integral membrane proteins.

The (2)H,(13)C,(15)N-labeled, 148-residue integral membrane protein OmpX from Escherichia coli was reconstituted with dihexanoyl phosphatidylcholine (DHPC) in mixed micelles of molecular mass of about 60 kDa. Transverse relaxation-optimized spectroscopy (TROSY)-type triple resonance NMR experiments and TROSY-type nuclear Overhauser enhancement spectra were recorded in 2 mM aqueous solutions of these mixed micelles at pH 6.8 and 30 degrees C. Complete sequence-specific NMR assignments for the polypeptide backbone thus have been obtained. The (13)C chemical shifts and the nuclear Overhauser effect data then resulted in the identification of the regular secondary structure elements of OmpX/DHPC in solution and in the collection of an input of conformational constraints for the computation of the global fold of the protein. The same type of polypeptide backbone fold is observed in the presently determined solution structure and the previously reported crystal structure of OmpX determined in the presence of the detergent n-octyltetraoxyethylene. Further structure refinement will have to rely on the additional resonance assignment of partially or fully protonated amino acid side chains, but the present data already demonstrate that relaxation-optimized NMR techniques open novel avenues for studies of structure and function of integral membrane proteins.

==About this Structure==

1ORM is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli]. Full crystallographic information is available from [http://~~ispc~~.weizmann.ac.il/oca-bin/ocashort?id=1ORM OCA].

1ORM is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1ORM OCA].

==Reference==

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[[Category: trosy]]

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@@ Line 1: / Line 1: @@
-[[Image:1orm.jpg|left|200px]]<br /><applet load="1orm" size="450" color="white" frame="true" align="right" spinBox="true"
+[[Image:1orm.jpg|left|200px]]<br /><applet load="1orm" size="350" color="white" frame="true" align="right" spinBox="true"
 caption="1orm" />
 '''NMR FOLD OF THE OUTER MEMBRANE PROTEIN OMPX IN DHPC MICELLES'''<br />
 ==Overview==
-The (2)H,(13)C,(15)N-labeled, 148-residue integral membrane protein OmpX, from Escherichia coli was reconstituted with dihexanoyl, phosphatidylcholine (DHPC) in mixed micelles of molecular mass of about 60, kDa. Transverse relaxation-optimized spectroscopy (TROSY)-type triple, resonance NMR experiments and TROSY-type nuclear Overhauser enhancement, spectra were recorded in 2 mM aqueous solutions of these mixed micelles at, pH 6.8 and 30 degrees C. Complete sequence-specific NMR assignments for, the polypeptide backbone thus have been obtained. The (13)C chemical, shifts and the nuclear Overhauser effect data then resulted in the, identification of the regular secondary structure elements of OmpX/DHPC in, solution and in the collection of an input of conformational constraints, for the computation of the global fold of the protein. The same type of, polypeptide backbone fold is observed in the presently determined solution, structure and the previously reported crystal structure of OmpX determined, in the presence of the detergent n-octyltetraoxyethylene. Further, structure refinement will have to rely on the additional resonance, assignment of partially or fully protonated amino acid side chains, but, the present data already demonstrate that relaxation-optimized NMR, techniques open novel avenues for studies of structure and function of, integral membrane proteins.
+The (2)H,(13)C,(15)N-labeled, 148-residue integral membrane protein OmpX from Escherichia coli was reconstituted with dihexanoyl phosphatidylcholine (DHPC) in mixed micelles of molecular mass of about 60 kDa. Transverse relaxation-optimized spectroscopy (TROSY)-type triple resonance NMR experiments and TROSY-type nuclear Overhauser enhancement spectra were recorded in 2 mM aqueous solutions of these mixed micelles at pH 6.8 and 30 degrees C. Complete sequence-specific NMR assignments for the polypeptide backbone thus have been obtained. The (13)C chemical shifts and the nuclear Overhauser effect data then resulted in the identification of the regular secondary structure elements of OmpX/DHPC in solution and in the collection of an input of conformational constraints for the computation of the global fold of the protein. The same type of polypeptide backbone fold is observed in the presently determined solution structure and the previously reported crystal structure of OmpX determined in the presence of the detergent n-octyltetraoxyethylene. Further structure refinement will have to rely on the additional resonance assignment of partially or fully protonated amino acid side chains, but the present data already demonstrate that relaxation-optimized NMR techniques open novel avenues for studies of structure and function of integral membrane proteins.
 ==About this Structure==
-ORM is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1ORM OCA].
+ORM is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1ORM OCA].
 ==Reference==
@@ Line 25: / Line 25: @@
 [[Category: trosy]]
-''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 23:07:56 2007''
+''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:20:48 2008''