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Protein folding remains a formidable challenge despite significant advances, particularly in sequence-to-structure prediction. Accurately capturing thermodynamics and intermediates via simulations demands overcoming time scale limitations, making effective collective variable (CV) design for enhanced sampling crucial. Here, we introduce a strategy to automatically construct complementary, bioinspired CVs. These uniquely capture local hydrogen bonding─explicitly distinguishing protein-protein from protein-water interactions─and side-chain packing, taking into account both native and non-native contacts to enhance state resolution. Using these CVs in combination with advanced enhanced sampling methods, we simulate the folding of Chignolin and TRP-cage, validating our approach against extensive unbiased simulations. Our results accurately resolve complex free-energy landscapes, reveal critical intermediates such as the dry molten globule, and demonstrate agreement with reference data. This interpretable and portable strategy underscores the critical role of microscopic details in protein folding, opening up a promising avenue for studying larger and more-complex biomolecular systems.
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http://dx.doi.org/10.1021/acs.jpclett.5c02079 | DOI Listing |
J Agric Food Chem
September 2025
School of Chemical Engineering and Technology, Zhengzhou University, Zhengzhou 450001, China.
d-Amino acid oxidase from (DAAO) is valuable for pharmaceutical and chemical synthesis due to its high enantioselectivity, but its poor thermostability limits extensive application. This study proposed a synergistic strategy of "sequence consensus design coupled with structure modification" to enhance DAAO thermostability. Through homologous sequence analysis and greedy algorithm-based optimization, a triple mutant M3 (S18T/V7I/Y132F) was obtained, showing a 3.
View Article and Find Full Text PDFJCI Insight
September 2025
Division of Metabolism, Endocrinology & Diabetes, and.
Intracellular trafficking of secretory and membrane proteins from the endoplasmic reticulum (ER) to the cell surface, via the secretory pathway, is crucial to the differentiated function of epithelial tissues. In the thyroid gland, a prerequisite for such trafficking is proper protein folding in the ER, assisted by an array of ER molecular chaperones. One of the most abundant of these chaperones, Glucose-Regulated-Protein-170 (GRP170, encoded by Hyou1), is a noncanonical hsp70-like family member.
View Article and Find Full Text PDFInt J Biol Macromol
September 2025
Institute of Cytology Russian Academy of Sciences, St. Petersburg, Russia; Laboratory of structural dynamics, stability and folding of proteins, Institute of Cytology Russian Academy of Sciences, 4 Tikhoretsky ave., 194064, St. Petersburg, Russia. Electronic address:
Growing evidence links gut microbiota to neurodegenerative diseases, yet direct molecular interactions between bacterial and host amyloid proteins remain incompletely understood. Bacterial amyloids represent an understudied yet potentially critical component of gut-brain communication in neurodegeneration. Here, we provide the first investigation of whether amyloids formed by outer membrane proteins (OMPs) of enterobacteria can modulate neurodegeneration-associated protein aggregation.
View Article and Find Full Text PDFDev Comp Immunol
September 2025
Institute of Entomology, College of Life Sciences, Nankai University, Tianjin, 300071, China. Electronic address:
The phylum Mollusca is one of the most diverse groups, second only to arthropods, whose production through aquaculture and wild capture is increasing due to its nutritional and economic values, especially its protein availability for human consumption. However, the negative influence caused by pathogen infection and environmental challenges has led to low aquaculture productivity and economic losses for shellfish farmers. Heat shock proteins, as molecular chaperones, contribute to the folding of nascent proteins, environmental adaptation, the immune response, etc.
View Article and Find Full Text PDFJ Phys Chem Lett
September 2025
School of Pharmaceutical Sciences, University of Geneva, Rue Michel-Servet 1, CH-1206 Geneva, CH, Switzerland.
Protein folding remains a formidable challenge despite significant advances, particularly in sequence-to-structure prediction. Accurately capturing thermodynamics and intermediates via simulations demands overcoming time scale limitations, making effective collective variable (CV) design for enhanced sampling crucial. Here, we introduce a strategy to automatically construct complementary, bioinspired CVs.
View Article and Find Full Text PDF