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RATIONALEApplication of Fourier transform ion cyclotron (FT‐ICR) tandem mass spectrometry reveals the binding sites for novel cyclopentadienyl IrIII anticancer complexes on calmodulin. The conventional fragmentation methods, collisionally activated dissociation (CAD) and infrared multiphoton dissociation (IRMPD), failed to define the Ir modification, but these binding sites were located via electron...
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