Solid-phase DNA sequencing reactions performed in micro-capillary reactors and solid-phase reversible immobilization in microfluidic chips for purification of dye-labeled DNA sequencing fragments | Posted on:2004-06-18 | Degree:Ph.D | Type:Dissertation | University:Louisiana State University and Agricultural & Mechanical College | Candidate:Xu, Yichnan | Full Text:PDF | GTID:1461390011474065 | Subject:Biology | Abstract/Summary: | | The research presented in this dissertation involves micro-capillary reactors for solid-phase DNA sequencing, the identification of dye-terminator sequencing fragments with time-resolved methods, and purification of dye-labeled DNA fragments using solid-phase reversible immobilization in microfluidic chips.;Solid-phase micro-reactors have been prepared for DNA sequencing applications using slab gel electrophoresis. A PCR product was immobilized to the interior wall of a fused-silica capillary tube via a biotin-streptavidin linkage. Solid-phase sequencing was carried out in micro-capillary reactors using a four-lane, single color dye primer chemistry strategy. The read length was found to be 589 bases. The complementary DNA fragments generated in the small volume (∼62 nL) reactor were directly injected into the gel-filled capillary for size separation with detection accomplished using near-IR laser-induced fluorescence.;A set of terminators labeled with near-IR heavy-atom modified tricarbocyanine dyes were investigated for a terminator sequencing protocol in conjunction with slab gel electrophoresis. This protocol gave 605 by read lengths. A one color, two lifetime format of DNA sequencing was implemented. A pixel-by-pixel analysis was employed to identify each of the bases in the run. The resulting read accuracy for the two-dye capillary run was 90.6%.;The use of photoactivated polycarbonate (PC) for purification of dye-labeled terminator sequencing fragments using solid-phase reversible immobilization (SPRI) was investigated. SPRI cleanup of dye-terminator sequencing fragments using a photoactivated PC microchannel and slab gel electrophoresis produce a read length of 620 bases with a calling accuracy of 98.9%. The PC-SPRI cleanup format was also integrated to a capillary gel electrophoresis system. In this case, the immobilization microchannel contained microposts to increase the loading level of DNAs to improve signal intensity without the need for pre-concentration. | Keywords/Search Tags: | DNA, Solid-phase, Micro-capillary reactors, Slab gel electrophoresis, Purification, Dye-labeled | | Related items |
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