1py0

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(New page: 200px<br /><applet load="1py0" size="450" color="white" frame="true" align="right" spinBox="true" caption="1py0, resolution 2.00&Aring;" /> '''Crystal structure of...)
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[[Image:1py0.gif|left|200px]]<br /><applet load="1py0" size="350" color="white" frame="true" align="right" spinBox="true"
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'''Crystal structure of E51C/E54C Psaz from A.faecalis with CLaNP probe'''<br />
'''Crystal structure of E51C/E54C Psaz from A.faecalis with CLaNP probe'''<br />
==Overview==
==Overview==
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A lanthanide complex, named CLaNP (caged lanthanide NMR probe) has been, developed for the characterisation of proteins by paramagnetic NMR, spectroscopy. The probe consists of a lanthanide chelated by a derivative, of DTPA (diethylenetriaminepentaacetic acid) with two thiol reactive, functional groups. The CLaNP molecule is attached to a protein by two, engineered, surface-exposed, Cys residues in a bidentate manner. This, drastically limits the dynamics of the metal relative to the protein and, enables measurements of pseudocontact shifts. NMR spectroscopy experiments, on a diamagnetic control and the crystal structure of the probe-protein, complex demonstrate that the protein structure is not affected by probe, attachment. The probe is able to induce pseudocontact shifts to at least, 40 A from the metal and causes residual dipolar couplings due to alignment, at a high magnetic field. The molecule exists in several isomeric forms, with different paramagnetic tensors; this provides a fast way to obtain, long-range distance restraints.
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A lanthanide complex, named CLaNP (caged lanthanide NMR probe) has been developed for the characterisation of proteins by paramagnetic NMR spectroscopy. The probe consists of a lanthanide chelated by a derivative of DTPA (diethylenetriaminepentaacetic acid) with two thiol reactive functional groups. The CLaNP molecule is attached to a protein by two engineered, surface-exposed, Cys residues in a bidentate manner. This drastically limits the dynamics of the metal relative to the protein and enables measurements of pseudocontact shifts. NMR spectroscopy experiments on a diamagnetic control and the crystal structure of the probe-protein complex demonstrate that the protein structure is not affected by probe attachment. The probe is able to induce pseudocontact shifts to at least 40 A from the metal and causes residual dipolar couplings due to alignment at a high magnetic field. The molecule exists in several isomeric forms with different paramagnetic tensors; this provides a fast way to obtain long-range distance restraints.
==About this Structure==
==About this Structure==
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1PY0 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Alcaligenes_faecalis Alcaligenes faecalis] with ZN, Y1, SO4 and YMA as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1PY0 OCA].
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1PY0 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Alcaligenes_faecalis Alcaligenes faecalis] with <scene name='pdbligand=ZN:'>ZN</scene>, <scene name='pdbligand=Y1:'>Y1</scene>, <scene name='pdbligand=SO4:'>SO4</scene> and <scene name='pdbligand=YMA:'>YMA</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1PY0 OCA].
==Reference==
==Reference==
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[[Category: Alcaligenes faecalis]]
[[Category: Alcaligenes faecalis]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Boulanger, M.J.]]
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[[Category: Boulanger, M J.]]
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[[Category: Hupkes, H.J.]]
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[[Category: Hupkes, H J.]]
[[Category: Impagliazzo, A.]]
[[Category: Impagliazzo, A.]]
[[Category: Kosters, W.]]
[[Category: Kosters, W.]]
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[[Category: Murphy, M.E.]]
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[[Category: Murphy, M E.]]
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[[Category: Peters, J.A.]]
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[[Category: Peters, J A.]]
[[Category: Prudencio, M.]]
[[Category: Prudencio, M.]]
[[Category: Rohovec, J.]]
[[Category: Rohovec, J.]]
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[[Category: nmr probe]]
[[Category: nmr probe]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 00:13:24 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:33:43 2008''

Revision as of 12:33, 21 February 2008


1py0, resolution 2.00Å

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Crystal structure of E51C/E54C Psaz from A.faecalis with CLaNP probe

Overview

A lanthanide complex, named CLaNP (caged lanthanide NMR probe) has been developed for the characterisation of proteins by paramagnetic NMR spectroscopy. The probe consists of a lanthanide chelated by a derivative of DTPA (diethylenetriaminepentaacetic acid) with two thiol reactive functional groups. The CLaNP molecule is attached to a protein by two engineered, surface-exposed, Cys residues in a bidentate manner. This drastically limits the dynamics of the metal relative to the protein and enables measurements of pseudocontact shifts. NMR spectroscopy experiments on a diamagnetic control and the crystal structure of the probe-protein complex demonstrate that the protein structure is not affected by probe attachment. The probe is able to induce pseudocontact shifts to at least 40 A from the metal and causes residual dipolar couplings due to alignment at a high magnetic field. The molecule exists in several isomeric forms with different paramagnetic tensors; this provides a fast way to obtain long-range distance restraints.

About this Structure

1PY0 is a Single protein structure of sequence from Alcaligenes faecalis with , , and as ligands. Full crystallographic information is available from OCA.

Reference

A caged lanthanide complex as a paramagnetic shift agent for protein NMR., Prudencio M, Rohovec J, Peters JA, Tocheva E, Boulanger MJ, Murphy ME, Hupkes HJ, Kosters W, Impagliazzo A, Ubbink M, Chemistry. 2004 Jul 5;10(13):3252-60. PMID:15224334

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