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Fraaije, M. W.

Publications and source records attributed to Fraaije, M. W..

3 recordsLinked to original sources

The evolution and mechanistic versatility of the bacterial NADH dehydrogenases type II

Type II NADH dehydrogenases (NDH-2s) are accessory enzymes of the bacterial electron transport chain (ETC). While they functionally overlap with Complex I, their main role is not proton translocation but maintaining the intracellular NADH/NAD+ balance. Although often non-essential, NDH-2 become crucial in species lacking complex I, serving as the primary electron entry point into the ETC. Their virtual absence in mammals makes these enzymes attractive targets for antimicrobial drug development and mitochondrial functional restoration. NDH-2s catalyze electron transfer from NADH to quinones, yet two distinct catalytic mechanisms have been described for members of the family: a classical ping-pong mechanism and an atypical ternary mechanism involving the formation of a charge transfer complex (CTC). The molecular basis of these mechanisms remains unclear. Also, their occurrence among NDH-2s from different bacterial lineages in unknown. Here we combined molecular phylogenetics, ancestral sequence reconstruction, expression and biochemical characterization of ancestral and modern enzymes and, molecular dynamics simulations to explore the mechanistic versatility of NDH-2s across Bacteria. Our results show the atypical ternary mechanism is restricted to the Firmicutes (Bacillota) lineage and it is defined by the presence of a single substitution located at the bottom of the active site. This work provides an evolutionary framework for understanding NDH-2 mechanistic versatility. Besides, it establishes a basis for drug discovery targeting pathogenic strains and opens avenues to develop innovative strategies to complement dysfunctional mitochondria.

biochemistry↗

Condition-dependent, amorphous protein agglomerates control cytoplasmic rheology

Molecular crowding in the bacterial cytoplasm restricts the diffusion of large molecules, impacting cellular processes. However, how nutrient availability influences cytoplasmic rheology is not well understood. With single-particle tracking in Escherichia coli, we observed a threefold variation in the diffusion of a 40-nm particle across exponential growth conditions. Previously suggested determinants of rheology did not account for this variation; instead, we found a strong anticorrelation between the diffusion coefficient and the abundance of amino acid metabolism proteins, persisting upon genetic perturbations and showing that lower diffusion is associated with increased viscoelasticity. Photoactivated light microscopy revealed that some amino acid metabolism proteins form clusters. Electron microscopy showed that these proteins could form amorphous agglomerates at physiological concentrations in vitro, likely driven by their low intrinsic disorder, high compactness and hydropathy score. These findings show that protein agglomerates regulate cytoplasmic rheology in a condition-dependent manner, suggesting an underappreciated level of cytoplasmic organization. HighlightsO_LIDiffusion of 40-nm particles varies threefold across growth conditions in E. coli C_LIO_LICytoplasmic diffusion inversely correlates with COG-E protein abundance COG-E proteins form agglomerates that increase cytoplasmic viscoelasticity C_LIO_LIProtein compactness and hydrophobicity predict condition-dependent crowding effects C_LI

biophysics↗

Investigating the mechanisms of enzyme diffusion using mass photometry

The existence of the phenomenon of enhanced enzyme diffusion (EED) has been a topic of debate in recent literature. One proposed mechanism to explain the origin of EED is oligomeric enzyme dissociation. We use mass photometry (MP), a label-free single-molecule technique, to investigate the dependence of the oligomeric states of several enzymes on their ligands. The studied enzymes of interest are catalase, aldolase, alkaline phosphatase and vanillyl-alcohol oxidase (VAO). We compared the ratios of oligomeric states in the presence and absence of substrate as well as different substrate and inhibitor concentrations. Catalase and aldolase were found to dissociate into smaller oligomers in the presence of their substrates, independently of inhibition, while for alkaline phosphatase and VAO, different behaviors were observed. Thus, we have identified a possible mechanism which explains the previously observed diffusion enhancement in vitro. This enhancement may occur due to the dissociation of oligomers through ligand binding.

biophysics↗