α-Glucosidase inhibition by luteolin: Kinetics, interaction and molecular docking

International Journal of Biological Macromolecules

Volumn 64, Issue , 2014, Pages 213-223

  Yan, Jiakai ^a   Zhang, Guowen ^a   Pan, Junhui ^a   Wang, Yajie ^a  

^a NANCHANG UNIVERSITY   (China)

Author keywords

Inhibition kinetics; Interaction; Luteolin; Molecular docking; Glucosidase

Indexed keywords

ALPHA GLUCOSIDASE; LUTEOLIN;

ARTICLE; BINDING AFFINITY; CATALYSIS; CIRCULAR DICHROISM; CONFORMATIONAL TRANSITION; ENERGY TRANSFER; ENTHALPY; ENTROPY; ENZYME ACTIVITY; ENZYME INHIBITION; ENZYME KINETICS; ENZYME MODIFICATION; FLUORESCENCE ANALYSIS; FOURIER TRANSFORM INFRARED PHOTOACOUSTIC SPECTROSCOPY; HUMAN; HYDROPHOBICITY; MATHEMATICAL ANALYSIS; MOLECULAR DOCKING; PROTEIN BINDING; PROTEIN FUNCTION; PROTEIN INTERACTION; PROTEIN STRUCTURE;

INHIBITION KINETICS; INTERACTION; LUTEOLIN; MOLECULAR DOCKING; Α-GLUCOSIDASE;

ALPHA-GLUCOSIDASES; AMINO ACID SEQUENCE; BINDING SITES; ENZYME ACTIVATION; ENZYME INHIBITORS; KINETICS; LUTEOLIN; MOLECULAR DOCKING SIMULATION; MOLECULAR SEQUENCE DATA; MOLECULAR STRUCTURE; PROTEIN BINDING; PROTEIN CONFORMATION; SEQUENCE ALIGNMENT; THERMODYNAMICS;

EID: 84890964329     PISSN: 01418130     EISSN: 18790003     Source Type: Journal    
DOI: 10.1016/j.ijbiomac.2013.12.007     Document Type: Article

References (52)

1. Lim E.L., Hollingsworth K.G., Aribisala B.S., Chen M.J., Mathers J.C., Taylor R. Diabetologia 2011, 54:2506-2514.
2. Bisht S., Kant R., Kumar V. Int. J. Biol. Macromol. 2013, 59:214-220.
3. Hu X.J., Wang X.B., Kong L.Y. J. Agric. Food Chem. 2013, 61:1501-1508.
4. Wang Y.f., Yang Z.W., Wei X.L. Int. J. Biol. Macromol. 2010, 47:534-539.
5. Charron M.J., Dubin R.A., Michels C.A. Mol. Cell. Biol. 1986, 6:3891-3899.
6. Luo H., Imoto T., Hiji Y. World J. Gastroenterol. 2001, 7:270-274.
7. Wehmeier U.F., Piepersberg W. Appl. Microbiol. Biotechnol. 2004, 63:613-625.
8. Kumar S., Narwal S., Kumar V., Prakash O. Pharmacogn. Rev. 2011, 5:19-29.
9. Li Y.Q., Zhou F.C., Gao F., Bian J.S., Shan F. J. Agric. Food Chem. 2009, 57:11463-11468.
10. Shi S.Y., Zhang Y.P., Xiong X., Huang K.L., Chen X.Q., Peng M.J. Food Chem. 2012, 135:1083-1090.
11. Papadopoulou A., Green R.J., Frazier R.A. J. Agric. Food Chem. 2005, 53:158-163.
12. Zhang Y.P., Shi S.Y., Chen X.Q., Zhang W., Huang K.L., Peng M.J. J. Agric. Food Chem. 2011, 59:8499-8506.
13. Odetti P.R., Borgoglio A., De P.A., Rolandi R., Adezati L. Diabetes 1990, 39:796-801.
14. Srinivasan K., Kaul C.L., Ramarao P. Indian J. Pharm. 2005, 37:327-328.
15. Je H.D., Shin C.Y., Park S.Y., Yim S.H., Kum C., Huh I.H., Kim J.H., Sohn U.D. Arch. Pharm. Res. 2002, 25:184-190.
16. Nagasawa T., Tabata N., Ito Y., Aiba Y., Nishizawa N., Kitts D.D. Mol. Cell Biochem. 2003, 252:141-147.
17. Chieko A., Nobuyuki T., Shizuka H., Kanako N., Shan L., Taku U., Tsuyoshi G., Rina Y., Joji N., Shigeru M., Teruo K. FEBS Lett. 2009, 583:3649-3654.
18. Middleton E., Kandaswami C., Theoharides T.C. Pharmacol. Rev. 2000, 52:673-751.
19. Matsui T., Kobayashi M., Hayashida S., Matsumoto K. Biosci. Biotechnol. Biochem. 2002, 66:689-692.
20. Minpei K., Katsura I., Yoshihiro M. Nat. Prod. Commun. 2012, 7:471-474.
21. Kenjiro T., Yuji M., Kouta T., Tomoko M. J. Nutr. Sci. Vitaminol. 2006, 52:149-153.
22. Kim J.S., Kwon C.S., Son K.H. Biosci. Biotechnol. Biochem. 2000, 64:2458-2461.
23. Zhang G.W., Ma Y.D., Wang L., Zhang Y.P., Zhou J. Food Chem. 2012, 133:264-270.
24. Herskovits T.T., Gadegbeku B., Jaillet H. J. Biol. Chem. 1970, 245:2588-2598.
25. Ohta T., Sasaki S., Oohori T., Yoshikawa S., Kurihara H. Biosci. Biotechnol. Biochem. 2002, 66:1552-1554.
26. Lee H.J., Lee H.S., Choi J.W., Ra K.S., Kim J.M., Suh H.J. J. Agric. Food Chem. 2011, 59:11522-11525.
27. Si Y.X., Wang Z.J., Park D., Chung H.Y., Wang S.F., Yan L., Yang J.M., Qian G.Y., Yin S.J., Park Y.D. Int. J. Biol. Macromol. 2012, 50:257-262.
28. Bi S.Y., Sun Y.T., Qiao C.Y., Zhang H.Q., Liu C.M. J. Lumin. 2009, 129:541-547.
29. Lakowicz J.R. Principles of Fluorescence Spectroscopy 2006, Springer Publications, New York. 3rd ed.
30. Liu M., Zhang W., Qiu L., Lin X.K. J. Biochem. 2011, 149:27-33.
31. Förster T., Sinanoglu O. Modern Quantum Chemistry 1966, Academic Press, New York.
32. Brindis F., Rodríguez R., Bye R., Gonzalez-Andrade M., Mata R. J. Nat. Prod. 2011, 74:314-320.
33. Escandón R.S., González A.M., Bye R., Linares E., Navarrete A., Mata R. J. Nat. Prod. 2012, 75:968-974.
34. Ali H.I., Fujita T., Akaho E., Nagamatsu T. J. Comput. Aided Mol. Des. 2010, 24:57-75.
35. Zeng Y.F., Lü Z.R., Yan L., Oh S., Yang J.M., Lee J., Ye Z.M. Process Biochem. 2012, 47:2284-2290.
36. Zeng Y.F., Lee J., Si Y.X., Yan L., Kim T.R., Qian G.Y., Lü Z.R., Ye Z.M., Yin S.J. Process Biochem. 2012, 47:2510-2517.
37. Ross P.D., Subramanian S. Biochemistry 1981, 20:3096-3102.
38. Kandagal P.B., Shaikh S.M.T., Manjunatha D.H., Seetharamappa J., Nagaralli B.S. J. Photochem. Photobiol. A 2007, 189:121-127.
39. Wang Q., Yan J., He J.W., Bai K.K., Li H. J. Lumin. 2013, 138:1-7.
40. Bani-Yaseen A.D. J. Lumin. 2011, 131:1042-1047.
41. Zhang H., Liu R.T., Chi Z.X., Gao C.Z. Spectrochim. Acta A 2011, 78:523-527.
42. Du Z.Y., Liu R.R., Shao W.Y., Mao X.P., Ma L., Gu L.Q., Huang Z.S., Chan A.S.C. Eur. J. Med. Chem. 2006, 41:213-218.
43. Shen Q., Shao J., Peng Q., Zhang W., Ma L., Chan A.S., Gu L. J. Med. Chem. 2010, 53:8252-8259.
44. Mandeville J.S., Froehlich E., Tajmir-Riahi H.A. J. Pharm. Biomed. Anal. 2009, 49:468-474.
45. Elkins K.M. J. Forensic Sci. 2011, 56:1580-1587.
46. Khan S.N., Islam B., Yennamalli R., Sultan A., Subbarao N., Khan A.U. Eur. J. Pharm. Sci. 2008, 35:371-382.
47. Surewicz W.K., Mantsch H.H., Chapman D. Biochemistry 1993, 2:389-394.
48. Zhang G.W., Wang L., Pan J.H. J. Agric. Food Chem. 2012, 60:2721-2729.
49. Pogozheva I.D., Przydziai M.J., Mosberg H.I. Drug Addiction 2008, 559-584.
50. Park H., Hwang K.Y., Kim Y.H., Oh K.H., Lee J.Y., Kim K. Bioorg. Med. Chem. 2008, 18:3711-3715.
51. Yamamoto K., Miyake H., Kusunoki M., Osaki S. FEBS J. 2010, 227:4205-4214.
52. Park H., Hwang K.Y., Oh K.H., Kim Y.H., Lee J.Y., Kim K. Bioorg. Med. Chem. 2008, 16:284-293.