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Thermodynamic analyses using ESI-MS revealed that cellular copper transport follows a gradient of increasing binding affinity, with Cu + binding to GSH ( K d~10 −13 M) at lower affinity than to dedicated copper chaperones such as antioxidant 1 copper chaperone (ATOX1), copper chaperone for superoxide dismutase (CCS), or cytochrome oxidase copper chaperone COX17 (COX17) 197