Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2049221 | FEBS Letters | 2010 | 4 Pages |
Abstract
ATP7B is a copper dependent P-type ATPase, required for copper homeostasis. Taking advantage of high yield heterologous expression of recombinant protein, we investigated charge transfer in ATP7B. We detected charge displacement within a single catalytic cycle upon ATP addition and formation of phosphoenzyme intermediate. We attribute this charge displacement to movement of bound copper within ATP7B. Based on specific mutations, we demonstrate that enzyme activation by copper requires occupancy of a site in the N-terminus extension which is not present in other transport ATPases, as well as of a transmembrane site corresponding to the cation binding site of other ATPases.
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Authors
Francesco Tadini-Buoninsegni, Gianluca Bartolommei, Maria Rosa Moncelli, Rajendra Pilankatta, David Lewis, Giuseppe Inesi,