Table 1.
Quantitation Methods | Advantages | Disadvantages | Metal Drugs Investigated by Each Method |
---|---|---|---|
ICAT | Procedure is easy. | Only two samples can be labeled, which is only applicable to proteins containing cysteine. | Cisplatin [43,44] |
TMT | Quantification on multiple sets of protein samples. | Expensive | Cisplatin [45] |
iTRAQ | Quantification on multiple sets of protein samples. | Expensive | Cisplatin [44] |
SILAC | Applicable to cultured cell. | It cannot be applied to samples such as tissues and body fluids. Expensive, time-consuming, and complicated. | Cisplatin [46] Gold (III) porphyrins [35] |
LFQP | Straightforward and cost-effective. | It requires more rigorous analytical measurements and statistical validation than isotope-coded measurements. | Cisplatin [47] [Pd(sac)(terpy)](sac) [48] Plecstatin [49] RAPTA agent [50] |
2-DE MS | It resolves thousands of intact protein species in a single run. | Time-consuming and labor-intense. | Cisplatin [51] Auranofin [52] Auoxo6 [52] Gold (III) NHC complexes [53] |