Prevention of insulin fibrillation by biocompatible choline-amino acid based ionic liquids: Biophysical insights

被引:5
|
作者
Judy, Eva [1 ]
Kishore, Nand [1 ,2 ]
机构
[1] Indian Inst Technol, Dept Chem, Mumbai 400076, India
[2] Indian Inst Technol, Mumbai 400076, Maharashtra, India
关键词
Biocompatible ionic liquids; Isothermal titration calorimetry; Differential scanning calorimetry; Aggregation; fibrillation; Insulin stabilization; PROTEIN AGGREGATION; THIOFLAVIN-T; BINDING; STABILITY; MECHANISM; DISEASES; PEPTIDE; MODEL;
D O I
10.1016/j.biochi.2022.11.013
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
We have synthesized biocompatible ionic liquids (ILs) with choline as cation and amino acids as anions to explore their potential towards prevention of fibrillation in insulin and the obtain corresponding mechanistic insights. This has been achieved by examining the effect of these ILs on insulin at the nucleation, elongation and maturation stages of the fibrillation process. A combination of high sensitivity isothermal titration calorimetry (ITC) and differential scanning calorimetry (DSC) have been employed along with spectroscopy and microscopy to evaluate interaction of the ILs at each stage of fibrillation quantitatively. Choline glycinate is observed to provide maximum stabilization to insulin compared to that provided by choline prolinate, choline leucinate, and choline valinate. This increased thermal sta-bilization has direct correlation with the extent of reduction in the fibrillation of insulin by ILs deter-mined using Thioflavin T and 8-anilinonaphthalene sulfonate based fluorescence assays. ITC has permitted understanding nature of interaction of the ILs with the protein at different fibrillation stages in terms of standard molar enthalpy of interaction whereas DSC has enabled understanding the extent of reduction in thermal stability of the protein at these stages. These ILs are able to completely inhibit formation of insulin aggregates at a concentration of 50 mM. Stabilization of proteins by ILs could be explained based on involvement of preferential hydration process. The work provides biocompatible IL based approach in achieving stability and prevention of fibrillation in insulin.(c) 2022 Elsevier B.V. and Societe Francaise de Biochimie et Biologie Moleculaire (SFBBM). All rights reserved.
引用
收藏
页码:20 / 32
页数:13
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