Skip to main content
Log in

Synthesis of polyacrylamide gel beads with electrostatic functional groups for the molecular imprinting of bovine serum albumin

  • Original Paper
  • Published:
Analytical and Bioanalytical Chemistry Aims and scope Submit manuscript

Abstract

Synthetic materials capable of recognizing proteins are important in separation, biosensors and biomaterials. In this study, bovine serum albumin-imprinted soft-wet polyacrylamide gel beads were prepared via inverse-phase suspension polymerization, using acrylamide and N,N′-methylene diacrylamide as polymeric matrix components and methacrylic acid as functional monomer. The adsorption study showed, through the imprinting process, that the imprinted gel beads had much higher adsorption capacity than the nonimprinted gel beads, and that the matching of the surface zeta-potential between the templates and the imprinted gel beads can enhance the imprinting effect. Adsorption kinetics indicated that the adsorption process could be described as an apparent first-order kinetic process for the gel beads. From the adsorption isotherm curve, we found that the adsorption of the imprinted gel beads was in agreement with the Langmuir adsorption model. Moreover, selectivity testing of the imprinted gel beads showed that imprinted gel beads exhibited good recognition for BSA as compared to the control protein. We speculate that the formation of complementary shapes and multiple-point electrostatic interactions between the imprinting cavities and the template proteins are the two factors that lead to the imprinting effect.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8
Fig. 9

Similar content being viewed by others

References

  1. Cormack PAG, Mosbach K (1999) React Funct Polym 41:115–124

    Article  CAS  Google Scholar 

  2. Wulff G (1995) Angew Chem Int Edit 31:1812–1832

    Google Scholar 

  3. Ansell RJ, Mosbach KJ (1997) J Chromatogr A 787:55–66

    Google Scholar 

  4. Chen W, Liu F, Xu Y, Li KA (2001) Anal Chim Acta 432: 277–282

    Article  CAS  Google Scholar 

  5. Cheong SH, Mcniven S, Uezu K, Goto M, Furusaki S (1997) Macromolecules 30: 1317–1322

    Article  CAS  Google Scholar 

  6. Lu SL, Cheng GX, Pang XS (2003) J Appl Polym Sci 89:3790–3796

    Article  CAS  Google Scholar 

  7. Zhang LY, Cheng GX, Fu C (2003) React Funct Polym 56:167–173

    Article  CAS  Google Scholar 

  8. Kempe M, Glad M, Mosbach K (1995) J Mol Recognit 8:35

    Google Scholar 

  9. Hjerten S, Liao J-L, Nakazato K, Wang Y, Zamaratskaina G, Zhang H-Y (1997) Chromatographia 44: 227–234

    Article  CAS  Google Scholar 

  10. Hirayama K, Burow M, Morikawa K, Minoura N (1998) Chem Lett 731

  11. Shi HQ, Tsai W, Garrison MD, Ferrari S, Ratner BD (1999) Nature 398:593–597

    Article  PubMed  CAS  Google Scholar 

  12. Ou SH, Wu MC, Chou TC, Liu CC (2004) Anal Chim Acta 504:163–166

    Article  CAS  Google Scholar 

  13. Pang XS, Cheng GX, Li RS, Lu SL, Zhang YH (2005) Anal Chim Acta 550:13–17

    Article  CAS  Google Scholar 

  14. Piletsky SA, Andersson HS, Nicholls IA (1999) Macromolecules 32:633–636

    Article  CAS  Google Scholar 

  15. Yin G, Liu Z, Zhan J, Ding FX, Yuan NJ (2002) Chem Eng J 87:181–186

    Article  CAS  Google Scholar 

Download references

Acknowledgements

The authors would like to thank the National Natural Science Foundation of China (grant number: 50373032) and the Teaching and Research Award Program for Outstanding Young Teachers in Higher Education Institutions of MOE, P.R.C. (2002–123) for supporting this research work.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Guoxiang Cheng.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Pang, X., Cheng, G., Lu, S. et al. Synthesis of polyacrylamide gel beads with electrostatic functional groups for the molecular imprinting of bovine serum albumin. Anal Bioanal Chem 384, 225–230 (2006). https://doi.org/10.1007/s00216-005-0147-x

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00216-005-0147-x

Keywords

Navigation