Comparative two-dimensional Fourier transform infrared correlation spectroscopic study on the spontaneous, pressure-, and temperature-enhanced H/D exchange in α-lactalbumin

被引:20
作者
Dzwolak, W
Kato, M
Shimizu, A
Taniguchi, Y
机构
[1] Ritsumeikan Univ, Coll Sci & Engn, Dept Appl Chem, Shiga 5258577, Japan
[2] Soka Univ, Fac Engn, Dept Bioengn, Hachioji, Tokyo 192, Japan
关键词
two-dimensional correlation spectroscopy; 2D/FT-IR; H/D exchange; second-derivative FT-IR; amide band; proteins; alpha-lactalbumin; high pressure;
D O I
10.1366/0003702001950689
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
Two-dimensional Fourier transform infrared FT-IR was applied for the examination of the H/D exchange process in D2O solutions of bovine alpha-lactalbumin. The slow spontaneous H/D exchange at 25 degrees C was compared with pressure-enhanced and temperature-enhanced H/D exchange. The HID-exchange process, which takes 48 h at 25 degrees C and under atmospheric pressure, is completed within 3 h when pressure is gradually elevated up to 180 MPa, or when temperature is increased up to 42.5 degrees C, Although the slow room-temperature HID exchange and the fast pressure or temperature-enhanced H/D exchange feature a high degree of similarity between the corresponding second-derivative spectra, the two-dimensional (2D) FT-IR correlation maps revealed that upon the heat treatment the order in which the H/D exchange takes place in the structural domains of alpha-lactalbumin is altered. It has been observed that these differences can be explained in light of the known properties of alpha-lactalbumin and the crystallographic data.
引用
收藏
页码:963 / 967
页数:5
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