The Malaysian Journal of Analytical Sciences, Vol 12 No 2 (2008): 302 - 309
L. Noumie Surugau1*, Ed T. Bergström2,
David M. Goodall3
1School of
Science and Technology, Universiti Malaysia Sabah,
Locked Bag 2073, 88999 Kota Kinabalu,
Sabah, Malaysia.
2Department of
Chemistry, University of York, Heslington, York, YO10 5DD, UK.
3Paraytec Ltd.,
1a St. George’s Place, Tadcaster Road, York, YO24 1GN, UK.
*Corresponding author: lnoumie@ums.edu.my
Capillary electrophoresis (CE) of nine peptides namely,
bradykinin, bradykinin fragment 1-5, substance P, Arg8-vasopressin,
luteinizing hormone-releasing hormone (LHRH), bombesin, leucine-enkephalin,
methionine-enkephalin and oxytocin were carried out using 0.5 % and 1.0 %
formic acid (FA) as the separation buffers, added with acetonitrile (ACN) and
triethylamine (TEA) as an additive at low pH. The electrophoretic behaviour of
these peptides was examined at different concentration of TEA (0, 10, 20, 30,
40 and 50 mM), and ACN (30, 40, 50, 60, 70 %) at their respective measured
final pH. The results showed that all nine peptides were fully resolved with
addition of 10 – 20 mM TEA. Peak efficiency was improved significantly by
increasing TEA concentration up to 40 mM where 800 000 m-1 was obtained.
Without TEA, the closely related enkephalins were co-migrating. Interestingly,
by addition of as little as 5 mM TEA has sufficient to separate them almost at
baseline. Increasing ACN to 40 % has
shortened the analysis time by ca. 1 min. However, further increase of ACN can
cause peak broadening and current instability.
Keywords: Peptides; Triethylamine, Formate, Acetonitrile,
Selectivity; Resolution
1. Corradini, D. 1997. J. Chromatogr. B, 699, 221.
2. Bullock, J.A., Yuan, L.C. 1991. J.
Microcolum Sep. 3, 241.
3. Nahum, A., Horvath, C. 1981. J.
Chromatogr. 203, 53.
4. Biij, K.E., Horvath, C., Melander, W.R. 1987. Nahum, A., J.
Chromatogr. 203, 65.
5. Riekkola, M.-L. 2002. Electrophoresis
23, 386.
6. Miller, C., Rivier, J. 1998. J. Pept.
Res. 51, 444.
7. Sarmini, K., Kenndler, E.
1997. J. Chromatogr. A, 792, 3.
8. Fujiwara, S., Honda, S. 1986. Anal.
Chem. 58, 1811.
9.
Idei, M. 1992. J. Liq. Chrom. 15, 3181.
10. Cherkaoui, S., Veuthey, J.-L. 2002. Electrophoresis,
23, 442.
11. Ensing, K., de Boer, T., Schreuder, N., de Zeeuw, R. 1999.
J.
Chromatogr. B, 727, 53.
12. Samskog, J., Wetterhall, M., Jacobsson, S., Markides,
K. 2000. J. Mass Spectrom. 35, 919.
13. Tachibana, Y., Otsuka, K.,
Terabu, S., Arai, A., Suzuki, K., Nakamura, S. 2003. J. of
Chromatogr. A, 1011, 181.
14. Peyrin, E., Guillaume, Y. C. 1999. J.
Chromatogr. A, 849, 563.
15. Yoshida, T., Okada, T. 1999. J.
Chromatogr. A, 840, 1.
16. Lee, H.G., Desiderio, D.M. 1997. J.
Chromatogr. Biomed. Sci. Appl. 28:
691 (1), 67.
17. Yang, Q., Benson, L. M., Johnson, K.L., Naylor, S. 1999.
J.
Biochem. Biophys. Methods 38,
103.