Missense mutations in MMACHC protein from cblC disease affect its conformational stability and vitamin B12-binding activity: The example of R161Q mutation

Longo, Lisa ; Randazzo, Loredana ; Bollati, Michela ; Carrotta, Rita ; Costa, Maria Assunta ; De Rosa, Matteo ; Mangione, Maria Rosalia ; Martorana, Vincenzo ; Culletta, Giulia ; Tutone, Marco ; Mari, Eleonora ; Ortore, Maria Grazia ; Garcia-Franco, Paula M. ; Velazquez-Campoy, Adrian (Universidad de Zaragoza) ; Passantino, Rosa ; Vilasi, Silvia

Resumen: MMACHC protein plays a crucial role in the metabolism of vitamin B12 (cobalamin, Cbl) by catalyzing its conversion into the active forms adenosylcobalamin (AdoCbl) and methylcobalamin (MeCbl), which serve as essential cofactors in key cellular reactions. Mutations in the gene encoding MMACHC lead to the rare metabolic disorder known as methylmalonic aciduria and homocystinuria, cblC type. This condition predominantly affects children and is characterized by cardiovascular dysfunction, intellectual disability, and a severe form of maculopathy. The most common missense mutation, R161Q, impairs enzymatic activity despite not being directly involved in cobalamin binding. Here, using a comprehensive set of biophysical techniques, we demonstrate that this pathogenic variant compromises MMACHC structural stability, alters the thermal unfolding cooperativity and pathway, as well as the populations of conformational intermediates. Moreover, we show that the R161Q mutation decreases AdoCbl binding affinity and impairs the protein's ability to form homodimers, which are supposed to have a functional role. A partial recovery in protein activity upon treatment with betaine, an osmolyte known for its stabilizing effect on proteins, was observed. This suggests a direct correlation between the energetics of MMACHC thermal unfolding and its functional activity. These findings contribute to a deeper understanding of the molecular mechanisms underlying MMACHC function and open avenues for potential therapeutic interventions.

Idioma: Inglés

DOI: 10.1016/j.ymgme.2025.109150

Año: 2025

Publicado en: Molecular genetics and metabolism 145, 3 (2025), 109150 [14 pp.]
ISSN: 1096-7192

Tipo y forma: Artículo (Versión definitiva)

Área (Departamento): Área Bioquímica y Biolog.Mole. (Dpto. Bioq.Biolog.Mol. Celular)