A facile method for determining ice recrystallization inhibition by antifreeze proteins

被引:81
|
作者
Tomczak, MM
Marshall, CB
Gilbert, JA
Davies, PL [1 ]
机构
[1] Queens Univ, Dept Biochem, Kingston, ON K7L 3N6, Canada
[2] Queens Univ, Prot Engn Network Ctr Excellence, Kingston, ON K7L 3N6, Canada
关键词
antifreeze protein; ice crystals; recrystallization inhibition; thermal hysteresis;
D O I
10.1016/j.bbrc.2003.10.106
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ice recrystallization, the growth of large ice crystals at the expense of small ones, stresses freeze tolerant organisms and causes spoilage of frozen foods. This process is inhibited by antifreeze proteins (AFPs). Here, we present a simple method for determining the ice recrystallization inhibition (RI) activity of an AFP under physiological conditions using 10 mul glass capillaries. Serial dilutions were prepared to determine the concentration below which RI activity was no longer detected, termed the RI endpoint. For type III AFP this was 200 nM. The capillary method allows samples to be aligned and viewed simultaneously, which facilitates RI endpoint determination. Once prepared, the samples can be used reproducibly in subsequent RI assays and can be archived in a freezer for future reference. This method was used to detect the elution of type III AFP from a Sephadex G-75 size-exclusion column. RI activity was found at the expected V-e for a 7 kDa protein and also unexpectedly in the void volume. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:1041 / 1046
页数:6
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