Phytochelatins
Bind Zn(II) with Micro- to Picomolar
Affinities without the Formation of Binuclear Complexes, Exhibiting
Zinc Buffering and Muffling Rather than Storing Functions
posted on 2024-06-07, 04:13authored byMarek Łuczkowski, Weronika Leszczyńska, Joanna Wątły, Stephan Clemens, Artur Krężel
Phytochelatins (PCs) are poly-Cys peptides containing
a repeating
γ-Glu-Cys motif synthesized in plants, algae, certain fungi,
and worms by PC synthase from reduced glutathione. It has been shown
that an excess of toxic metal ions induces their biosynthesis and
that they are responsible for the detoxification process. Little is
known about their participation in essential metal binding under nontoxic,
basal conditions under which PC synthase is active. This study presents
spectroscopic and thermodynamic interactions with the PC2–PC5
series, mainly focusing on the relations between Zn(II) complex stability
and cellular Zn(II) availability. The investigations employed mass
spectrometry, UV–vis spectroscopy, potentiometry, competition
assays with zinc probes, and isothermal titration calorimetry (ITC).
All peptides form ZnL complexes, while ZnL2 was found only
for PC2, containing two to four sulfur donors in the coordination
sphere. Binuclear species typical of Cd(II)-PC complexes are not formed
in the case of Zn(II). Results demonstrate that the affinity for Zn(II)
increases linearly from PC2 to PC4, ranging from micro- to low-picomolar.
Further elongation does not significantly increase the stability.
Stability elevation is driven mainly by entropic factors related to
the chelate effect and conformational restriction rather than enthalpic
factors related to the increasing number of sulfur donors. The affinity
of the investigated PCs falls within the range of exchangeable Zn(II)
concentrations (hundreds of pM) observed in plants, supporting for
the first time a role of PCs both in buffering and in muffling cytosolic
Zn(II) concentrations under normal conditions, not exposed to zinc
excess, where short PCs have been identified in numerous studies.
Furthermore, we found that Cd(II)-PC complexes demonstrate significantly
higher metal capacities due to the formation of polynuclear species,
which are lacking for Zn(II), supporting the role of PCs in Cd(II)
storage (detoxification) and Zn(II) buffering and muffling. Our results
on phytochelatins’ coordination chemistry and thermodynamics
are important for zinc biology and understanding the molecular basis
of cadmium toxicity, leaving room for future studies.