Literature DB >> 14505073

Is Ag(I) an adequate probe for Cu(I) in structural copper-metallothionein studies? The binding features of Ag(I) to mammalian metallothionein 1.

Oscar Palacios1, Kasia Polec-Pawlak, Ryszard Lobinski, Mercè Capdevila, Pilar González-Duarte.   

Abstract

The binding abilities of silver(I) to mammalian MT 1 have been studied and compared with those of copper(I), recently reported [Bofill et al. (2001) J Biol Inorg Chem 6:408-417], with the aim of analyzing the suitability of Ag(I) as a Cu(I) probe in Cu-MT studies. The Zn/Ag replacement in recombinant mouse Zn(7)-MT 1 and corresponding Zn(4)-alphaMT 1 and Zn(3)-betaMT 1 fragments, as well as the stepwise incorporation of Ag(I) to the corresponding apo-MTs, have been followed in parallel by various spectroscopic techniques including electronic absorption (UV-vis), circular dichroism (CD) and electrospray mass spectrometry coupled to capillary zone electrophoresis (CZE-ESI-MS). A comparative analysis of the sets of data obtained in the titration of Zn(7)-MT 1, Zn(4)-alphaMT 1 and Zn(3)-betaMT 1 with AgClO(4) at pH 7.5 and 2.5 has led to the reaction pathways followed during the incorporation of silver to these proteins under these specific conditions, disclosing unprecedented stoichiometries and structural features for the species formed. Thus, the Zn/Ag replacement in Zn(7)-MT 1 at pH 7.5 has revealed the subsequent formation of Ag(4)Zn(5)-MT, Ag(7)Zn(3)-MT, Ag(8)Zn(3)-MT, Ag(10)Zn(2)-MT, Ag(12)Zn(1)-MT, Ag(x)-MT, x=14-19, whose structure consists of two additive domains only if Zn(II) remains coordinated to the protein. A second structural role for Zn(II) has been deduced from the different folding found for the Ag(x)-MT species of the same stoichiometry formed at pH 7.5 or 2.5. Comparison of the binding features of Cu(I) and Ag(I) to the entire MT at pH 7.5 shows that, among all the micro(x)Zn(y)-MT (0<or= y<7) species found, only M(I)(4)Zn(5)-MT [(Zn(4))(alpha)(micro(4)Zn(1))(beta)] and M(I)(7)Zn(3)-MT [(micro(3)Zn(2))(alpha)(micro(4)Zn(1))(beta)], which form during the first stages of the Zn(II)/M(I) metal replacement, show comparable 3D structures; thus, they are the only species where Ag(I) ions can be predicted to be an adequate probe for Cu(I).

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Year:  2003        PMID: 14505073     DOI: 10.1007/s00775-003-0481-4

Source DB:  PubMed          Journal:  J Biol Inorg Chem        ISSN: 0949-8257            Impact factor:   3.358


  19 in total

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Journal:  J Biol Inorg Chem       Date:  2002-02-07       Impact factor: 3.358

5.  Refined crystal structure of Cd, Zn metallothionein at 2.0 A resolution.

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Authors:  R K Mehra; K Tran; G W Scott; P Mulchandani; S S Saini
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8.  Monitoring of the metal displacement from the recombinant mouse liver metallothionein Zn(7)-complex by capillary zone electrophoresis with electrospray MS detection.

Authors:  Kasia Połeć Pawlak; Oscar Palacios; Mercè Capdevila; Pilar González-Duarte; Ryszard Lobiński
Journal:  Talanta       Date:  2002-07-03       Impact factor: 6.057

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Authors:  J Domenech; O Palacios; L Villarreal; P González-Duarte; M Capdevila; S Atrian
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10.  Spectroscopic studies of copper and silver binding to metallothioneins.

Authors:  M J Stillman
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  7 in total

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6.  Probing structural changes in the alpha and beta domains of copper- and silver-substituted metallothionein by emission spectroscopy and electrospray ionization mass spectrometry.

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7.  CRISP-R/Cas9 Mediated Deletion of Copper Transport Genes CTR1 and DMT1 in NSCLC Cell Line H1299. Biological and Pharmacological Consequences.

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  7 in total

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