Lactose and Galactose Promote the Crystallization of Human Galectin-10.
Yu-Fan FuSi-Cong JiangZhong-Wei ZhangXin-Yue YangZi-Lin LiJing HuShu YuanPublished in: Molecules (Basel, Switzerland) (2023)
Galectin-10 (Gal-10) forms Charcot-Leyden crystals (CLCs), which play a key role in the symptoms of asthma and allergies and some other diseases. Gal-10 has a carbohydrate-binding site; however, neither the Gal-10 dimer nor the CLCs can bind sugars. To investigate the monomer-dimer equilibrium of Gal-10, high-performance size-exclusion chromatography (SEC) was employed to separate serial dilutions of Gal-10 with and without carbohydrates. We found that both the dimerization and crystallization of Gal-10 were promoted by lactose/galactose binding. A peak position shift for the monomer was observed after treatment with either lactose or galactose, implying that the polarity of the monomer was reduced by lactose/galactose binding. Further experiments indicated that alkaline conditions of pH 8.8 mimicked the lactose/galactose-binding environment, and the time interval between monomers and dimers in the chromatogram decreased from 0.8 min to 0.4 min. Subsequently, the electrostatic potential of the Gal-10 monomers was computed. After lactose/galactose binding, the top side of the monomer shifted from negatively charged to electrically neutral, allowing it to interact with the carbohydrate-binding site of the opposing subunit during dimerization. Since lactose/galactose promotes the crystallization of Gal-10, our findings implied that dairy-free diets (free of lactose/galactose) might be beneficial to patients with CLC-related diseases.
Keyphrases
- molecularly imprinted
- endothelial cells
- chronic obstructive pulmonary disease
- mass spectrometry
- magnetic resonance imaging
- dna binding
- computed tomography
- risk assessment
- physical activity
- magnetic resonance
- molecular dynamics
- high speed
- cystic fibrosis
- diffusion weighted imaging
- simultaneous determination
- protein kinase
- tandem mass spectrometry