Structure and properties of licochalcone A-human serum albumin complexes in solution: A spectroscopic, photophysical and computational approach to understand drug-protein interaction

Physical Chemistry Chemical Physics

Volumn 10, Issue 44, 2008, Pages 6597-6606

  Monti, Sandra ^a   Manet, Ilse ^a   Manoli, Francesco ^a   Marconi, Giancarlo ^a  

^a Istituto Per La Sintesi Organica E La Fotoreattività   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 55849109272     PISSN: 14639076     EISSN: None     Source Type: Journal    
DOI: 10.1039/b809241a     Document Type: Article

References (38)

1. A. Iuga, M. Spoerner, H. R. Kalbitzer, E. Brunner J. Mol. Biol., 2004, 342, 1033-1040
2. D. A. Snyder, Y. Chen, N. G. Denissova, T. Acton, J. M. Aramini, M. Ciano, R. Karlin, J. Liu, P. Manor, P. A. Rajan, P. Rossi, G. V. T. Swapna, R. Xiao, B. Rost, J. Hunt, G. T. Montelione J. Am. Chem. Soc., 2005, 127, 16505-16511
3. S. G. F. Rasmussen, H.-J. Choi, D. M. Rosenbaum, T. S. Kobilka, F. S. Thian, P. C. Edwards, M. Burghammer, V. R. P. Ratnala, R. Sanishvili, R. F. Fischetti, G. F. X. Schertler, W. I. Weis, B. K. Kobilka Nature, 2007, 450, 383-387
4. A. Yee, A. Savchenko, A. Ignachenko, J. Lukin, X. Xu, T. Skarina, E. Evdokimova, C. S. Liu, A. Semesi, V. Guido, A. M. Edwards, C. H. Arrowsmith J. Am. Chem. Soc., 2005, 127, 16512-16517
5. A. Grisaev, J. Wu, J. Trewhella, A. Bax J. Am. Chem. Soc., 2005, 127, 16621-16628
6. C. Jung J. Mol. Recognit., 2000, 13, 325-351
7. R. Tuma J. Raman Spectrosc., 2005, 36, 307-319
8. S. Monti, F. Manoli, S. Sortino, R. Morrone, G. Nicolosi Phys. Chem. Chem. Phys., 2005, 7, 4002-4008
9. S. Monti, I. Manet, F. Manoli, R. Morrone, G. Nicolosi, S. Sortino Photochem. Photobiol., 2006, 82, 13-19
10. S. Monti, I. Manet, F. Manoli, S. Sortino Photochem. Photobiol. Sci., 2007, 6, 462-470
11. S. Monti, I. Manet, F. Manoli, M. L. Capobianco, G. Marconi J. Phys. Chem. B, 2008, 112, 5742-5754
12. Z. Nowakowska Eur. J. Med. Chem., 2007, 42, 125-137. and references therein
13. R. Renan, Identification of the Traditional Chinese Materia Medica, Shangai Scientific and Technical Pub. House, Shanghai, People’s Republic of China, 1986
14. Friis-Møller M. Chen, K. Fuursted, S. B. Christensen, A. Kharazmi Planta Med., 2002, 68, 416-419
15. M. Chen, L. Zhai, S. B. Christensen, T. G. Theander, A. Kharazmi Antimicrob. Agents Chemother., 2001, 45, 2023-2029
16. M. Chen, T. Theander, S. B. Christensen, L. Hvid, L. Zhai, A. Kharazmi Antimicrob. Agents Chemother., 1994, 38, 1470-1475
17. A. Kharazmi, M. Chen, T. G. Theander, S. B. Christensen Ann. Trop. Med. Parasitol., 1997, 91, 91-95
18. H. L. Ziegler, H. S. Hansen, D. Staerk, S. B. Christensen, H. Hägerstrand, J. W. Jaroszewski Antimicrob. Agents Chemother., 2004, 48, 4067-4071
19. G. Marconi, S. Monti, F. Manoli, S. Ottani J. Inclusion Phenom. Macrocyclic Chem., 2007, 57, 279-282
20. W. He, Y. Li, J. Liu, Z. Hu, X. Chen Biopolymers, 2005, 79, 48-57
21. InsightII, Accelrys Software Inc., San Diego, CA, 2005
22. S. Sugio, A. Kashima, S. Mochizuki, M. Noda, K. Kobayashi Protein Eng., 1999, 12, 439-446
23. I. Tinoco, Jr Adv. Chem. Phys., 1962, 4, 113.
24. P. Bortolus, G. Marconi, S. Monti, B. Mayer, G. Kohler, G. Grabner Chem. Eur. J., 2000, 6, 1578-1591
25. MNDO, Hyperchem 6.02, Hypercube Inc., Gainesville, FL, 2000
26. S. W. Baldwin, in Organic Photochemistry, ed. A. Padwa, Marcel Dekker, New York, 1981, vol. 5, pp. 123-225
27. Stefanidis S. Cho, S. Dhe-Paganon, W. P. Jencks J. Am. Chem. Soc., 1993, 115, 1650-1656
28. M. Montalti, A. Credi, L. Prodi, and M. T. Gandolfi, Handbook of Photochemistry, CRC Taylor & Francis, Boca Raton, FL 33487-2742, 2006, p. 574
29. 2 as reference, afforded the same values as those calculated on the basis of the spectra of Fig. 3
30. Y.-H. Chen, J. T. Yang, H. Martinez Biochemistry, 1972, 11, 4120-4131
31. M. Dockal, D. C. Carter, F. Rüker J. Biol. Chem., 1999, 274, 29303-29310
32. J. R. Lakowicz, Principles of Fluorescence Spectroscopy, Kluwer Academic/Plenum Publisher, New York, 1999, ch. 16
33. calc
34. Attribution of similar emission efficiency to LA in both binding sites is consistent with the similarity of the emission quantum yields of 1 : 1 and 2 : 1 complexes
35. G. Sudlow, D. J. Birkett, D. N. Wade Mol. Pharmacol., 1976, 12, 1052-1061
36. For the role of triplet in chalcone cis-trans photoisomerization, see R. Caldwell, M. Singh J. Am. Chem. Soc., 1983, 105, 5139-5140
37. A. Siemiarczuk, C. E. Petersen, C.-E. Ha, J. Yang, N. V. Bhagavan Cell Biochem. Biophys., 2004, 40, 115-122.
38. W. Qiu, L. Zhang, O. Okobiah, Y. Yang, L. Wang, D. Zhong, A. Zewail J. Phys. Chem. B, 2006, 110, 10540-10549