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Cysteine Pathogenic Variants of PMM2 Are Sensitive to Environmental Stress with Loss of Structural Stability
Fan Yu1, Li Lin1, Jingmiao Sun1
1The Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou 310052, China.
Abstract:
Congenital disorders of glycosylation (CDG) are severe metabolic disorders caused by an imbalance in the glycosylation pathway. Phosphomannomutase2 (PMM2-CDG), the most prevalent CDG, is mainly due to the disorder of PMM2. Pathogenic variants in cysteine have been found in various diseases, and cysteine residues have a potential as therapeutic targets. PMM2 harbor six cysteines; the variants Cys9Tyr (C9Y) and Cys241Ser (C241S) of PMM2 have been identified to associate with CDG, but the underlying molecular mechanisms remain uncharacterized. Here, we purified PMM2 wild type (WT), C9Y, and C241S to investigate their structural characteristics and biophysical properties by spectroscopic experiments under physiological temperature and environmental stress. Notably, the variants led to drastic changes in the protein properties and were prone to aggregate at physiological temperature. Meanwhile, PMM2 was sensitive to oxidative stress, and the cysteine pathogenic variants led to obvious aggregate formation and a higher cellular apoptosis ratio under oxidative stress. Molecular dynamic simulations indicated that the pathogenic variants changed the core domain of homomeric PMM2 and subunit binding free energy. Moreover, we tested the potential drug targeting PMM2-celastrol in cell level and explained the result by molecular docking simulation. In this study, we delineated the pathological mechanism of the cysteine substitution in PMM2, which addressed the vital role of cysteine in PMM2 and provided novel insights into prevention and treatment strategies for PMM2-CDG.
Insights
Pathogenic variants in phosphomannomutase2 (PMM2) cause PMM2-congenital disorders of glycosylation (CDG). Cysteine variants disrupt PMM2 structure, leading to aggregation and apoptosis, suggesting cysteine as a therapeutic target for PMM2-CDG.
Area of Science:
- Biochemistry
- Molecular Biology
- Genetics
Background:
- Congenital disorders of glycosylation (CDG) are severe metabolic diseases.
- Phosphomannomutase2 deficiency (PMM2-CDG) is the most common CDG subtype.
- Cysteine residues in PMM2 are implicated in PMM2-CDG pathogenesis.
Purpose of the Study:
- Investigate the structural and biophysical impact of PMM2 cysteine variants (C9Y, C241S).
- Elucidate the molecular mechanisms underlying PMM2-CDG associated with cysteine substitutions.
- Explore potential therapeutic strategies targeting PMM2 for PMM2-CDG.
Main Methods:
- Protein purification of PMM2 wild type (WT), C9Y, and C241S variants.
- Spectroscopic experiments to assess structural characteristics and biophysical properties.
- Molecular dynamic simulations and molecular docking for mechanistic insights.
Main Results:
- PMM2 variants C9Y and C241S induced significant structural changes and aggregation at physiological temperatures.
- PMM2 exhibited sensitivity to oxidative stress, with cysteine variants exacerbating aggregation and apoptosis.
- Simulations revealed pathogenic variants alter PMM2's core domain and subunit interactions.
- Celastrol showed potential as a therapeutic agent targeting PMM2 in cellular assays.
Conclusions:
- Cysteine residues play a critical role in PMM2 stability and function.
- Cysteine substitutions in PMM2 are directly linked to PMM2-CDG pathology.
- Understanding these mechanisms offers new avenues for PMM2-CDG treatment strategies.
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