Table 1.
Glutathione | Trypanothione | |
---|---|---|
A. Chemical structure Oxidized state: |
Número de envío [A |
|
Reduced state: |
3552373] |
|
B. Enzymes involved | GshA and GshB | TryS |
C. Substrates | ATP L-Glutamate L-Cysteine L-Glycine |
ATP Spermidine GSH (*possibly synthesized by parasite) |
D. Reduction coefficient (Fairlamb and Cerami, 1992) | Eo = −0.230 | Eo = −0.242 V |
E. pKa (Moutiez et al., 1994) | 8.7 | 7.4 |
F. Concentration | 1 mM in blood (Richie et al., 1996). 6.9 mM in intracellular milieu of HeLa cells (Montero et al., 2013) |
0.12–0.64 nmol/108 epimastigotes; 0.25–0.95 nmol/108 bloodstream trypomastigotes; 0.12 nmol/108 amastigotes (Ariyanayagam and Fairlamb, 2001; Ariyanayagam et al., 2003) |
Glutathione (ubiquitous monothiol among eukaryotes) and trypanothione (a kinetoplastid-specific dithiol) are synthesized by parasites' antioxidant machinery, and these molecules play a key role in distribution of reducing equivalents along the antioxidant network. Even when they have similar characteristics, T[SH]2 is considered a kinetically superior antioxidant.