4.5 Article

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

Journal

JOURNAL OF PHYSICAL CHEMISTRY B
Volume -, Issue -, Pages -

Publisher

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

Keywords

-

Funding

  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]

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available