Selectivity in heavy metal- binding to peptides and proteins |
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Authors: | DeSilva Tara M Veglia Gianluigi Porcelli Fernando Prantner Andrew M Opella Stanley J |
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Affiliation: | Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, CA 92093, USA. |
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Abstract: | The metal-binding affinities and three-dimensional structures of three synthetic 18-residue peptides with sequences derived from that of the highly conserved metal-binding motif MXCXXC found in many heavy metal-binding proteins were determined. A change in register of the cysteines and alanines of the sequence from the periplasmic mercury-binding protein, MerP, i.e., CAAC, CACA, and CCAA, affects the specificity of metal binding, in particular, the peptide with vicinal cysteines binds only mercury. The three-dimensional structures of the mercury-bound forms of the three peptides determined in solution by NMR spectroscopy peptides differ considerably, even though they are all linear bicoordinate complexes. The three-dimensional structure of the peptide with CAAC bound to Cd(II) demonstrates that the metal-binding loop is malleable enough to accommodate modes of coordination other than linear bicoordinate. |
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Keywords: | mercury cadmium mercury‐binding protein NMR spectroscopy peptides |
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