Related ArticlesThe Cu(I)(7) cluster in yeast copper thionein survives major shortening of the polypeptide backbone as deduced from electronic absorption, circular dichroism, luminescence and( 1)H NMR.
J Biol Inorg Chem. 2003 Feb;8(3):353-9
Authors: Luchinat C, Dolderer B, Del Bianco C, Echner H, Hartmann HJ, Voelter W, Weser U
Owing to the frustrating experience of not being able to obtain crystalline yeast Cu(I)(7) -metallothionein, thereby allowing elucidation of the X-ray structure, truncated forms were prepared to facilitate possible crystallization. The mobile remnants at either the N- or C-terminal end of the polypeptide chain were omitted. In parallel with the crystallization efforts, it was of interest to examine the degree to which the shortening of the protein portion might affect the intactness of the Cu(I)(7) -thiolate cluster, thereby hampering their use as structural models for the intact protein. (1)H two-dimensional NMR spectroscopy at 800 MHz was performed on the intact wild-type yeast Cu(7)-thionein and on two truncated forms (peptide(-1-40) and peptide(5-40)). The NMR spectral data reveal, regardless of the length of the polypeptide chain, that the spin patterns were fully preserved with all relevant NOEs. The corresponding calculated structures were virtually identical. All other spectrometric properties, including circular dichroism, luminescence and electronic absorption, allowed the same conclusion. Minor differences were observed in the chiroptic and luminescent measurements. Interestingly, however, the resistance towards oxygen was progressively diminished with decreasing length of the polypeptide backbone. The half-life of the luminescence of the wild-type protein was 48 h while the luminescence of the shortest peptide levelled off within 24 h.
[NMR paper] A NMR study of the interaction of a three-domain construct of ATP7A with copper(I) and copper(I)-HAH1: the interplay of domains.
A NMR study of the interaction of a three-domain construct of ATP7A with copper(I) and copper(I)-HAH1: the interplay of domains.
Related Articles A NMR study of the interaction of a three-domain construct of ATP7A with copper(I) and copper(I)-HAH1: the interplay of domains.
J Biol Chem. 2005 Nov 18;280(46):38259-63
Authors: Banci L, Bertini I, Cantini F, Chasapis CT, Hadjiliadis N, Rosato A
ATP7A is a P-type ATPase involved in copper(I) homeostasis in humans. It possesses a long N-terminal tail protruding into the cytosol and containing six...
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[NMR paper] Proton NMR investigation of the [4Fe--4S]1+ cluster environment of nitrogenase iron p
Proton NMR investigation of the 1+ cluster environment of nitrogenase iron protein from Azotobacter vinelandii: defining nucleotide-induced conformational changes.
Related Articles Proton NMR investigation of the 1+ cluster environment of nitrogenase iron protein from Azotobacter vinelandii: defining nucleotide-induced conformational changes.
Biochemistry. 1995 Dec 5;34(48):15646-53
Authors: Lanzilotta WN, Holz RC, Seefeldt LC
This work presents the complete assignment of the isotropically shifted 1H NMR resonances of Azotobacter vinelandii...
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[NMR paper] 1H NMR investigation of the paramagnetic cluster environment in Pyrococcus furiosus t
1H NMR investigation of the paramagnetic cluster environment in Pyrococcus furiosus three-iron ferredoxin: sequence-specific assignment of ligated cysteines independent of tertiary structure.
Related Articles 1H NMR investigation of the paramagnetic cluster environment in Pyrococcus furiosus three-iron ferredoxin: sequence-specific assignment of ligated cysteines independent of tertiary structure.
Biochemistry. 1995 Jan 17;34(2):600-10
Authors: Gorst CM, Yeh YH, Teng Q, Calzolai L, Zhou ZH, Adams MW, La Mar GN
One- and two-dimensional 1H NMR...
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[NMR paper] Helix formation by the phospholipase A2 38-59 fragment: influence of chain shortening
Helix formation by the phospholipase A2 38-59 fragment: influence of chain shortening and dimerization monitored by nmr chemical shifts.
Related Articles Helix formation by the phospholipase A2 38-59 fragment: influence of chain shortening and dimerization monitored by nmr chemical shifts.
Biopolymers. 1994 May;34(5):647-61
Authors: Jiménez MA, Carreño C, Andreu D, Blanco FJ, Herranz J, Rico M, Nieto JL
The solution structure of a peptide fragment corresponding to the 38-59 region of porcine phospholipase A2 has been investigated using CD,...
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[NMR paper] Thiol/disulfide formation associated with the redox activity of the [Fe3S4] cluster o
Thiol/disulfide formation associated with the redox activity of the cluster of Desulfovibrio gigas ferredoxin II. 1H NMR and Mössbauer spectroscopic study.
Related Articles Thiol/disulfide formation associated with the redox activity of the cluster of Desulfovibrio gigas ferredoxin II. 1H NMR and Mössbauer spectroscopic study.
J Biol Chem. 1994 Mar 18;269(11):8052-8
Authors: Macedo AL, Moura I, Surerus KK, Papaefthymiou V, Liu MY, LeGall J, Münck E, Moura JJ
Desulfovibrio gigas ferredoxin II (FdII) is a small protein (alpha 4 subunit...
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[NMR paper] Helix formation by the phospholipase A2 38-59 fragment: influence of chain shortening
Helix formation by the phospholipase A2 38-59 fragment: influence of chain shortening and dimerization monitored by nmr chemical shifts.
Related Articles Helix formation by the phospholipase A2 38-59 fragment: influence of chain shortening and dimerization monitored by nmr chemical shifts.
Biopolymers. 1994 May;34(5):647-61
Authors: Jiménez MA, Carreño C, Andreu D, Blanco FJ, Herranz J, Rico M, Nieto JL
The solution structure of a peptide fragment corresponding to the 38-59 region of porcine phospholipase A2 has been investigated using CD,...
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08-22-2010 03:33 AM
[NMR paper] Thiol/disulfide formation associated with the redox activity of the [Fe3S4] cluster o
Thiol/disulfide formation associated with the redox activity of the cluster of Desulfovibrio gigas ferredoxin II. 1H NMR and Mössbauer spectroscopic study.
Related Articles Thiol/disulfide formation associated with the redox activity of the cluster of Desulfovibrio gigas ferredoxin II. 1H NMR and Mössbauer spectroscopic study.
J Biol Chem. 1994 Mar 18;269(11):8052-8
Authors: Macedo AL, Moura I, Surerus KK, Papaefthymiou V, Liu MY, LeGall J, Münck E, Moura JJ
Desulfovibrio gigas ferredoxin II (FdII) is a small protein (alpha 4 subunit...
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08-22-2010 03:33 AM
[NMR paper] Copper- and silver-substituted yeast metallothioneins: sequential 1H NMR assignments
Copper- and silver-substituted yeast metallothioneins: sequential 1H NMR assignments reflecting conformational heterogeneity at the C terminus.
Related Articles Copper- and silver-substituted yeast metallothioneins: sequential 1H NMR assignments reflecting conformational heterogeneity at the C terminus.
Biochemistry. 1993 Jul 6;32(26):6773-87
Authors: Narula SS, Winge DR, Armitage IM
Complete 1H NMR sequential assignments have been made for copper(I)- and silver (I)-substituted metallothionein (MT) from Saccharomyces cerevisiae using standard...