4.5 Article

Diffusion Coefficient of Intracrystalline Water in Intrinsic Hen Egg-White Lysozyme Crystals Determined by Confocal Raman Spectroscopy

期刊

JOURNAL OF PHYSICAL CHEMISTRY B
卷 -, 期 -, 页码 -

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcb.2c06329

关键词

-

资金

  1. PRESTO
  2. Japan Science and Technology Agency [JPMJPR1995]
  3. Japan Society for the Promotion of Science (JSPS) KAKENHI [17K06797, 19K23579]
  4. Iketani Science and Technology Foundation [0291078-A]

向作者/读者索取更多资源

This study determined the diffusion coefficient of intracrystalline water in intrinsic hen egg-white lysozyme (HEWL) crystals using confocal Raman spectroscopy and air convection with controlled relative humidity. The results provide valuable insights into the hydration mechanism of proteins and have practical applications in porous materials, drug binding, and cryoprotectant soaks.
Protein crystals composed of protein molecules are expected as a novel porous material. They have high porosity, and the knowledge of the diffusion of intracrystalline water is important. In this study, the diffusion coefficient of intracrystalline water in intrinsic hen egg-white lysozyme (HEWL) crystals was determined by a method that combines confocal Raman spectroscopy and air convection with controlled relative humidity. Similar to common porous materials, the drying process of the protein crystals includes three periods: constant-rate drying, falling-rate drying, and equilibrium state. During the falling-rate drying period, the drying rate depends on the diffusion of intracrystalline water in the protein crystal. The gradient of the water content was measured using confocal Raman spectroscopy. The diffusion coefficient of the intrinsic HEWL crystals was determined as 3.1 x 10-7 cm2/s with a water content of 36.3 vol %. The estimated diffusion coefficients of the intrinsic HEWL crystals without cross-linking were in close agreement with those of the cross-linked protein crystals. This study is timely as the knowledge of the intrinsic diffusion coefficient is useful not only for understanding the mechanism of hydration of proteins but also in practical applications such as porous materials, drug binding, and cryoprotectant soaks.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据