화학공학소재연구정보센터
Biochemical and Biophysical Research Communications, Vol.293, No.1, 7-12, 2002
Decreased subunit exchange of heat-treated lens alpha A-crystallin
alphaA-Crystallin high-molecular-weight (HMW) aggregates were prepared by preheating at 80-90 degreesC and studied using spectroscopic measurements. Conformational differences were suggested based on data of increased bis-ANS (4.4'-dianilino-1,1'-binaphthalene-5,5'-disulfonic acid) and ThT (thioflavin T) fluorescence as well as increased far-UV and decreased near-UV circular dichroism (CD). These results indicated that HMW aggregated alpha-crystallin was more hydrophobic than the native alpha-crystallin, possibly resulting from partial unfolding of alpha-crystallin. The two cysteines in alphaA-crystallin were mostly oxidized in HMW aggregates. The effects of HMW aggregation on the dynamic structure were studied with fluorescence resonance energy transfer; subunit exchange became slower. These results strongly suggest that HMW alphaA-crystallin aggregates result from exposure of buried beta-pleated sheets and increased hydrophobic interaction. (C) 2002 Elsevier Science (USA). All rights reserved.