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Thermal stability and hydration dynamics of Chymotrypsin Inhibitor 2 in aqueous amino acid solutions from replica exchange molecular dynamics | Synapse
March 3, 2026
Thermal stability and hydration dynamics of Chymotrypsin Inhibitor 2 in aqueous amino acid solutions from replica exchange molecular dynamics
RG
Rabiul Gazi
National Institute of Technology Rourkela
SM
Sankar N. Maity
National Institute of Technology Rourkela
MJ
Madhurima Jana
Key Points
Chymotrypsin Inhibitor 2 exhibits thermal stability, crucial for understanding protein behavior.
The analysis shows that hydration dynamics are significantly influenced by surrounding amino acid solutions.
Utilizing replica exchange molecular dynamics, the study explores how temperature alters protein interactions.
Understanding these dynamics may help improve protein formulations or therapeutic strategies in biochemistry.
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Cite This Study
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Gazi et al. (Wed,) studied this question.
synapsesocial.com/papers/69a76026c6e9836116a2c9c1
https://doi.org/https://doi.org/10.1016/j.bbrc.2026.153403