Skip to main content
. 2019 Dec 20;9:435. doi: 10.3389/fcimb.2019.00435

Table 1.

Trypanothione and glutathione are the major, low MW thiols utilized by T. cruzi to keep redox homeostasis.

Glutathione Trypanothione
A. Chemical structure
Oxidized state:
graphic file with name fcimb-09-00435-i0001.jpg Inline graphic
Número de envío [A
Reduced state: graphic file with name fcimb-09-00435-i0003.jpg Inline graphic
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.