Skip to main content
Log in

Large-scale oligonucleotide synthesizers

I. Basic principles and system design

  • Published:
Applied Biochemistry and Biotechnology Aims and scope Submit manuscript

Abstract

The central problem in scaling up oligonucleotide synthesis is to expose each element of a large bed to the same conditions obtaining in very small ones, for the same intervals of time. Our analysis suggests that scale-up is chiefly limited by fluid path length through the bed. By using annular beds in zonal centrifuge rotors of unique design, with fluid flow controlled by combining centrifugal force with differences in physical density between reagents, reagent fronts may be kept exactly perpendicular to the direction of flow in each bed element. Under these conditions, bed volume may be increased by increasing rotor length and diameter. The rotor is lined with polypropylene or Teflon®, and has a thick tempered glass end window. Transparent rotary valves of a unique design allow any of47 reagents to be selected and the direction of flow through the rotor to be controlled. A photodiode spectrophotometer provides complete absorption spectra on fluid in the rotor inlet and outlet lines every4 s, and a large balance weighs effluent from the synthesizer continuously. The entire operation is controlled by a work station, and steps may be programmed by time, absorbance, or reagent mass. Reagents are identified by spectra, and trityls are integrated on line. A detailed time-stamped log file provides a complete record of each synthesis.

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.

Similar content being viewed by others

References

  1. Riordan, M. L. and Martin, J. C. (1991),Nature 350, 442,443.

    Article  Google Scholar 

  2. Bonora, G. M., Biancotti, G., Maffini, M., and Scremin, C. L. (1993),Nucleic Acid Res. 21, 1213–1217.

    Article  CAS  Google Scholar 

  3. Carruthers, M. H. (1989), inOligonucleotides. Antisense Inhibitors of Gene Expression. Cohen, J. S., ed. CRC, Boca Raton, FL, pp. 7–24.

    Google Scholar 

  4. Gait, M. J. (1984),Oligonucleotide Synthesis. IRL Press, Oxford.

    Google Scholar 

  5. Haller, W. (1983), inSolid Phase Biochemistry, Scouten, W. H., ed. John Wiley, New York, pp. 535–597.

    Google Scholar 

  6. Anderson, N. G., ed. (1966),The Development of Zonal Centrifuges. National Cancer Institute. Monograph No. 21.

  7. Anderson, N. G., Waters, D. A., Nunley, C. E., Gibson, R. F., Schilling, R. M., Denny, E. C., Cline, G. B., Babelay, E. F., and Perardi, T. E. (1969),Anal. Biochem. 32, 460–494.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

anderson, N.G., Anderson, N.L., Taylor, J. et al. Large-scale oligonucleotide synthesizers. Appl Biochem Biotechnol 54, 19–42 (1995). https://doi.org/10.1007/BF02787909

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02787909

Index Entries

Navigation