Journal:Protein Science:4
From Proteopedia
Why is binding of a divalent metal cation to a structural motif containing four carboxylate residues not accompanied by a conformational change?Lushchekina, Weiner, Ashani, Emrizal, Firdaus-Raih, Silman & Sussman[1]  Torpedo californica acetylcholinesterase (TcAChE) contains a unique 4D motif composed of four aspartate residues that can bind divalent metal cations (like Ca²⁺, Mg²⁺, Mn²⁺), significantly increasing the enzyme’s thermal stability. Despite the electrostatic repulsion expected between these ]aspartates, structural analysis shows that the enzyme's conformation remains stable with or without bound cations as seen in an overlay the two states and an between them. The stability of the 4D motif is attributed to adjacent positively charged residues (Lys325, Arg388, and Arg517), forming stabilizing salt bridges, leading to the newly named 4A/3B motif (four acidic residues stabilized by three basic residues). The study also identified additional metal-binding sites (His264 and His471 sites) in TcAChE through crystallographic analysis, but these appear to be weaker or crystallographic artifacts. Using metadynamics and molecular dynamics (MD) simulations with quantum potentials (QM/MM-MD), the binding strength of metal cations at the 4D site was compared to that of the 4D site in human fibrin-stabilizing factor (fXIIIa), which lacks stabilizing cationic residues. Results showed that while TcAChE’s 4A/3B motif maintains structural integrity upon metal binding/unbinding, the fXIIIa motif is stable in presence of a metal ion but explodes without a metal ions due to electrostatic repulsion. This is seen clearly in an between these two states. The 4A/3B motif’s metal-binding strength is ~10 kcal/mol weaker than motifs with multiple anionic residues not surrounded by cationic residues. This flexibility. without conformational change. suggests the motif may act as a metal ion reservoir, potentially regulating metal concentrations. Similar motifs were found in other proteins, indicating a broader functional role beyond TcAChE. References
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