Effect of Non-Enzymatic Glycation on Cystatin: A Spectroscopic Study

被引:26
作者
Bhat, Sheraz Ahmad [1 ]
Sohail, Aamir [1 ]
Siddiqui, Azad Alam [1 ]
Bano, Bilqees [1 ]
机构
[1] Aligarh Muslim Univ, Fac Life Sci, Dept Biochem, Aligarh 202002, Uttar Pradesh, India
关键词
Maillard reaction; AGEs; Anti-papain; Chick pea cystatin; Glycation; HUMAN SERUM-ALBUMIN; MAILLARD REACTION; END-PRODUCTS; IMMUNOGLOBULIN-G; INHIBITORS; PROTEIN; GLYCERALDEHYDE; ENDPRODUCTS;
D O I
10.1007/s10895-014-1391-2
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
The study shows the effect of nonenzymatic glycation on conformation and inhibitory activity of chick pea cystatin (CPC). CPC was incubated with different reducing sugars, pentose (D-Ribose), hexoses (D-Glucose, D-Fructose) at 37 A degrees C for 5 weeks. To evaluate the modification of CPC by these different sugars during the glycation process the extent of the Maillard reaction, conformational, structural and functional changes were investigated. The behaviour of glycated CPC was monitored by the techniques of UV and fluorescence spectroscopies. Specific fluorescence was employed to characterise the glycation and AGEs. The anti-papain activity of glycated CPC was found to be significantly lower as compared to its non-glycated form. Glycation with ribose led to maximum loss in inhibitory activity. It was found that the incubation of CPC with all the mentioned sugars led to a parallel increase in tryptophan fluorescence as well as in Maillard and other AGEs specific fluorescence values and hyperchromicity in the UV-region. Among the sugars studied comparatively ribose was found to be the most active in inducing structural and conformational alterations in the protein suggesting its high reactivity with protein amino groups.
引用
收藏
页码:1107 / 1117
页数:11
相关论文
共 42 条
[1]
Ahmed N, 2002, BIOCHEM J, V364, P1
[2]
Advanced glycation endproducts - role in pathology of diabetic complications [J].
Ahmed, N .
DIABETES RESEARCH AND CLINICAL PRACTICE, 2005, 67 (01) :3-21
[3]
Acetonitrile can promote formation of different structural intermediate states on aggregation pathway of immunoglobulin G from human and bovine [J].
Amani, Samreen ;
Naeem, Aabgeena .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2011, 49 (01) :71-78
[4]
Baynes J W, 1989, Prog Clin Biol Res, V304, P43
[5]
Dynamics of ANS binding to tuna apomyoglobin measured with fluorescence correlation spectroscopy [J].
Bismuto, E ;
Gratton, E ;
Lamb, DC .
BIOPHYSICAL JOURNAL, 2001, 81 (06) :3510-3521
[6]
Bousova Iva, 2005, Acta Pharmaceutica (Zagreb), V55, P107
[7]
CYTOTOXIC EFFECT OF ADVANCED GLYCATION END PRODUCTS [J].
Boyanova, M. ;
Huppertz, B. .
BIOTECHNOLOGY & BIOTECHNOLOGICAL EQUIPMENT, 2009, 23 (01) :1072-1078
[8]
Bry L, 2001, CLIN CHEM, V47, P153
[9]
The use of capillary electrophoresis to monitor Maillard reaction products (MRP) by glyceraldehyde and the epsilon amino group of lysine [J].
de Sa, PFG ;
Treubig, JM ;
Brown, PR ;
Dain, JA .
FOOD CHEMISTRY, 2001, 72 (03) :379-384
[10]
Monitoring the effect of glucosamine and glyceraldehyde glycation on the secondary structure of human serum albumin and immunoglobulin G: An analysis based on circular dichroism, thermal melting profiles and UV-fluorescence spectroscopy [J].
Dutta, U ;
Cohenford, MA ;
Dain, JA .
ANALYTICA CHIMICA ACTA, 2006, 558 (1-2) :187-194