This talk will summarize our progress on the development of a method to sequence single DNA fragments. Our approach is based on single-molecule fluorescence detection [1] and consists of: labeling the different nucleotides types with distinguishable fluorophores; polymerase incorporation of the labeled nucleotides into a strand of DNA; attachment of one end of the DNA fragment to a suitable support; movement of the supported DNA into a flow stream to cause the DNA fragment to stretch out into the flow; exonuclease digestion of the free end of the fluorescently-labeled DNA strand to sequentially release the fluorophore-labeled nucleotides into the flow stream and efficient single-molecule detection and identification of the fluorophores in the ordered sample stream to read out the sequence. [2,3] The method has the potential for sequencing DNA fragments tens of thousands of bases in length, in contrast to current gel-electrophoresis-based sequencing methods with read lengths limited to approximately 1000 bases (1 kb). We have made considerable progress towards a demonstration of single DNA fragment sequencing. Up to three fluorophore-labeled nucleotide types have been incorporated into strands of DNA 2-7 kb in length. Only two of the nucleotide types need to be labeled at once; DNA can be sequenced in multiple passes using all combinations of labeling of the nucleotide types with two distinguishable labels. [4] Exonuclease turnover rates of ~50 and ~1 nucleotides per second have been measured at room temperature for Esherichia coli Exonuclease I and Exonuclease III, respectively, on fluorescently-labeled DNA. Multiple fragments of labeled DNA have been attached to polystyrene microspheres. Individual, DNA-laden microspheres have been optically trapped in flow ~30 microns upstream of a picoliter single-molecule fluorescence detection volume [5]. Exonuclease digestion of fluorescently-labeled DNA fragments attached to optically trapped microspheres has been monitored by the detection of individual, fluorophore-labeled nucleotides downstream of the microsphere. We have detected single, fluorophore-labeled nucleotides cleaved from as few as ~100 fragments of DNA held on an optically trapped microsphere. We have also used this capability to measure the turnover kinetics and to confirm the processivity of Exonuclease I on single-stranded, fluorescently-labeled DNA. Rhodamine-6G (R6G) and tetramethylrhodamine (TMR) labeled nucleotides (R6G-dCMP and TMR-dUMP), released by exonuclease digestion of labeled DNA fragments, have been detected and identified at the single-molecule level [6] by correlated measurements of fluorescence intensity and lifetime using a single excitation wavelength and detection channel [7]. This work is supported by the United States Department of Energy, Office of Biological and Environmental Research.

References

[1] Keller, R.A.; Ambrose, W.P.; Goodwin, P.M.; Jett, J.H.; Martin, J.C.; Wu, M. ``Single-molecule fluorescence analysis in solution,'' Appl. Spectrosc., 50:12A-32A (199 6).

[2] Goodwin, P.M.; Cai, H.; Jett, J.H.; Ishaug-Riley, S.L.; Machara, N.P.; Semin, D.J.; Van Orden, A.; Keller, R.A. ``Application of single-molecule detection to DNA sequencing,'' Nucleos. Nucleot., 16:543-550 (199 7).

[3] Jett, J.H.; Keller, R.A.; Martin, J.C.; Moyzis, R.K.; Ratliff, R.L.; Shera, E.B; Stewart, C.C. ``Method for Rapid Base Sequencing in DNA and RNA,'' US Patent #4,962,037 (199 0).

[4] Jett, J.H.; Keller, R.A.; Martin, J.C.; Posner, R.G.; Marrone, B.L.; Hammond, M.L.; Simpson, D.J. ``Method for Rapid Base Sequencing in DNA and RNA with Two Base Labeling,'' US Patent #5,405,747 (199 5).

[5] Machara, N.P.; Goodwin, P.M.; Enderlein, J.; Keller, R.A. ``Efficient detection of single molecules eluting off an optically trapped microsphere,'' Bioimaging, 6:33-42 (199 8).

[6] Werner, J.H.; Cai, H.; Goodwin, P.M.; Keller, R.A. ``Current status of DNA sequencing by single molecule detection,'' Proc. SPIE, 3602:355-366 (199 9).

[7] Van Orden, A.; Machara, N.P.; Goodwin P.M.; Keller, R.A. ``Single-molecule identification in flowing sample streams by fluorescence burst size and intraburst fluorescence decay rate,'' Anal. Chem., 70:1444-1451 (199 8).