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What the literature actually describes is better summarized as copper-dependent enzyme cofactor logistics: the complex participates in the movement of copper between ligands of differing affinity, and the downstream observations follow from where the copper ends up

Ibrahim KA, Abdelgaid HA, Eleyan M, Mohamed RA, Gamil NM

J Cell Biol 187:733747 Stehbens SJ, Paszek M, Pemble H, Ettinger A, Gierke S, Wittmann T (2014) CLASPs link focal-adhesion-associated microtubule capture to localized exocytosis and adhesion site turnover

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Here is why we do not use those sources, and why you should not either