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http://dx.doi.org/10.5012/bkcs.2011.32.9.3425

Solution State Structure of pA1, the Mimotopic Peptide of Apolipoprotein A-I, by NMR Spectroscopy  

Kim, Hyo-Joon (Department of Biochemistry and Molecular Biology, Hanyang University)
Won, Ho-Shik (Department of Applied Chemistry, Hanyang University)
Publication Information
Abstract
Apolipoprotein A-I (Apo A-I) is a major component for high density lipoproteins (HDL). A number of mimetic peptides of Apo A-I were screened from the phase-displayed random peptide library by utilizing monoclonal antibodies (A12). Mimetic peptide for A12 epitope against Apo A-I was selected as CPFARLPVEHHDVVGL (pA1). From the BLAST search, the mimetic peptide pA1 had 40% homology with Apo A-I. As a result of the structural determination of this mimotope using homo/hetero nuclear 2D-NMR techniques and NMR-based distance geometry (DG)/molecular dynamic (MD) computations, DG structure had low penalty value of 0.3-0.7 ${\AA}^2$ and the total RMSD was 0.6-1.6 ${\AA}$. The mimotope pA1 exhibited characteristic conformation including a ${\beta}$-turn from Pro[7] to His[11].
Keywords
Apolipoprotein A-I; NMR spectroscopy; Molecular dynamic computation;
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1 Schumaker, V. N.; Phillips, M. L.; Chatterton, J. E. Adv. Protein Chem. 1994, 45, 205.   DOI
2 Chen, S. H.; Yang, C. Y.; Chen, P. F.; Setzer, D.; Tamimura, M.; Li, W. H.; Gotto, A. M.; Chan, L. J. Biol. Chem. 1986, 261, 12918.
3 Segrest, J. P.; Jackson, R. L.; Morrisett, J. D.; Gotto, A. M. FEBS Lett. 1974, 38, 347.
4 Kaiser, E. T.; Kezdy, F. J. Science 1984, 223, 249.   DOI
5 Knott, T. J.; Pease, R. J.; Powell, L. M.; Wallis, S. C.; Rall, S. C., Jr.; Innerarity, R. L.; Blackhart, B.; Taylor, W. H.; Marcel, Y.; Milne, Y.; Johnson, D.; Fuller, M.; Lusis, A. J.; McCarthy, B. J.; Mahley, R. W.; Levy-Wilson, B.; Scott, J. Nature 1986, 323, 734.   DOI   ScienceOn
6 Borhani, D. W.; Rogers, D. P.; Engler, J. A.; Brouillette, C. G. Proc. Natl. Acad. Sci. U. S. A. 1997, 94, 12291.   DOI
7 Castelli, W. P.; Garrison, R. J.; Wilson, P. W. F.; Abbott, R. D.; Kalousdian, S.; Kannel, W. B. J. Am. Med. Assoc. 1986, 256, 2835.   DOI
8 Atkinson, D.; Davis, M. A. F.; Leslie, R. B. Proc. R. Soc. London 1974, 186, 165.   DOI
9 Segrest, J. P.; Jones, M. K.; De Loof, H.; Brouillette, C. G.; Venkatachalapathi, Y. V.; Anantharamaiah, G. M. J. Lipid Res. 1992, 33, 141.
10 Johnson, B. A.; Blevins, R. A. J. Biomol. NMR 1994, 4, 603.   DOI   ScienceOn
11 Wuthrich, K. NMR of Proteins and Nucleic Acids; Wiley: New York, 1986.
12 Evans, J. N. S. Biomolecular NMR Spectroscopy, Oxford Univ. Press, 1995.
13 South, T. L.; Blake, P. R.; Hare, D. R.; Summers, M. F. Biochemistry 1991, 30, 6342.   DOI   ScienceOn
14 Kim, D.; Rho, J.; Won, H. J. Korean Mag. Reson. Soc. 1999, 3, 44.
15 Cruzado, I. D.; Cockrill, S. L.; McNeal, C. J.; Macfarlane, R. D. J. Lipid Res. 1998, 39, 205.
16 Mahley, R. W.; Innerarity, T. L.; Rall, S. C., Jr.; Wesgraber, K. H. J. Lipid Res. 1984, 25, 1277.
17 Browman, B. H. Hepatic Plasma Proteins Mechanisms of Function and Regulation; Academic Press, Inc.: London, 1993.
18 Davis, R. A. Biochemistry of Lipids, Lipoproteins and Membranes; Elsevier Science Publishers: Canada, 1991.