4.5 Article

Mechanical Insight into Resistance of Betaine to Urea-Induced Protein Denaturation

Journal

JOURNAL OF PHYSICAL CHEMISTRY B
Volume 120, Issue 48, Pages 12327-12333

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcb.6b10172

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Funding

  1. National Natural Science Foundation of China [21234003]
  2. Fundamental Research Funds for the Central Universities

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It is known that urea can induce protein denaturation that can be inhibited by osmolytes. Yet, experimental explorations on this mechanism at the molecular level are still lacking. We have investigated the resistance of betaine to the urea-induced denaturation of lysozyme in aqueous solutions using low-field NMR. Our study demonstrates that urea molecules directly interact with lysozyme, leading to denaturation. However, betaine molecules interacting with urea more strongly than lysozyme can pull the bound urea molecules from lysozyme so that the protein is protected from denaturation. The number of urea molecules bound to a betaine molecule is given under different conditions. Proton NMR spectroscopy (H-1-NMR) and Fourier transform infrared spectroscopy reveal that the interaction between betaine and urea is through hydrogen bonding.

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