Inhibition of insulin fibrillation by osmolytes: Mechanistic Insights

被引:68
|
作者
Choudhary, Sinjan [1 ]
Kishore, Nand [2 ]
Hosur, Ramakrishna V. [1 ,3 ]
机构
[1] UM DAE Ctr Excellence Basic Sci, Bombay 400098, Maharashtra, India
[2] Indian Inst Technol, Dept Chem, Bombay 400076, Maharashtra, India
[3] Tata Inst Fundamental Res, Dept Chem Sci, Bombay 400005, Maharashtra, India
来源
SCIENTIFIC REPORTS | 2015年 / 5卷
关键词
AMYLOID FIBRILS; BOVINE INSULIN; COMPATIBLE SOLUTE; AGGREGATION; STABILIZATION; KINETICS; PROTECTION; STABILITY; PROTEINS; ECTOINE;
D O I
10.1038/srep17599
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We have studied here using a number of biophysical tools the effects of osmolytes, betaine, citrulline, proline and sorbitol which differ significantly in terms of their physical characteristics such as, charge distribution, polarity, H-bonding abilities etc, on the fibrillation of insulin. Among these, betaine, citrulline, and proline are very effective in decreasing the extent of fibrillation. Proline also causes a substantial delay in the onset of fibrillation in the concentration range (50-250 mM) whereas such an effect is seen for citrulline only at 250 mM, and in case of betaine this effect is not seen at all in the whole concentration range. The enthalpies of interaction at various stages of fibrillation process have suggested that the preferential exclusion of the osmolyte and its polar interaction with the protein are important in inhibition. The results indicate that the osmolytes are most effective when added prior to the elongation stage of fibrillation. These observations have significant biological implications, since insulin fibrillation is known to cause injection amyloidosis and our data may help in designing lead drug molecules and development of potential therapeutic strategies.
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页数:10
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