TABLE 3.
Different activation techniques applied for MS/MS-based characterization of sulfopeptides
| Activation method | Polarity | Samples analyzed | Advantage | Disadvantage | Reference |
|---|---|---|---|---|---|
|
| |||||
| MAD | Pos Neg | Model sulfopeptides | Retention and localization of SO3 | Low-efficiency long reaction period (~100 ms) biased cleavages next to acidic residues | Cook and Jackson (2011b) |
| niECD | Neg | Model sulfopeptides | Complete SO3 retention, good sequence coverage, minimal neutral loss products | Low efficiency due to long reaction time (1 s) | Hersberger and Håkansson (2012) |
| 193 nm UVPD | Neg | Model sulfopeptides | Retention and localization of SO3 | Dominant neutral loss of SO3 from the precursor and charge-reduced precursor ions | Robinson et al. (2014) |
| FRIPS | Neg | Model sulfopeptides | Retention and localization of SO3 | Not applied to complex samples | Borotto et al. (2018) |
| ETciD | Pos | Model sulfopeptides spiked into serum digest at 1:200, 1:1200, 1:2000 (w/w) | Positive mode is adaptable to existing workflows, retention and localization of SO3 | Poor sensitivity of very acidic sulfopeptides in positive mode | G. Chen et al. (2018) |
| HAD | Neg | Model sulfopeptides and bovine fibrinogen digest | Identified a sulfopeptide from fibrinogen digest using LC-MS/MS No charge reduced precursor | Low efficiency long reaction/accumulation time (1 min) | Asakawa et al. (2019) |