Advances in Single Molecule Nucleic Acid Sequencing

DNA;nucleic acids;nucleotides;polymerase;reverse transcriptase;RNA;sequencing;single-molecule

Lacenere, Christopher J. ; Quake, Stephen R.

University:California Institute of Technology

Department:Biology

关键词: DNA;    nucleic acids;    nucleotides;    polymerase;    reverse transcriptase;    RNA;    sequencing;    single-molecule;   

Others  :  https://thesis.library.caltech.edu/5252/1/thesis-c.lacenere.pdf

美国|英语

来源: Caltech THESIS

【 摘 要 】

The ability to quickly and accurately obtain sequence information from single molecules of DNA and RNA has far-reaching implications for our understanding of biology. In the work presented here, we have made several advances in the area of single-molecule DNA and RNA sequencing. Specifically, in attempting to increase the read length of DNA polymerase, we have assayed several custom synthesized fluorescent nucleotides containing longer dye–base linkers. We have validated the efficacy of these nucleotides at both bulk and single-molecule levels. Furthermore, we have screened several commercially available DNA polymerases for their ability to incorporate these nucleotides. We also show that reverse transcriptase is able to synthesize a complimentary DNA strand of 28 bases in length from an RNA template, using solely fluorescently labeled nucleotides. Additionally, we show that reverse transcriptase is able to incorporate a fluorescently labeled nucleotide into an RNA template at the single-molecule level. Finally, we demonstrate automated reagent exchange for our single-molecule sequencing system.