Issue 6, 2011

Integrated DNA purification, PCR, sample cleanup, and capillary electrophoresis microchip for forensic human identification

Abstract

A fully integrated microdevice and process for forensic short tandem repeat (STR) analysis has been developed that includes sequence-specific DNA template purification, polymerase chain reaction (PCR), post-PCR cleanup and inline injection, and capillary electrophoresis (CE). Fragmented genomic DNA is hybridized with biotin-labeled capture oligos and pumped through a fluidized bed of magnetically immobilized streptavidin-coated beads in microchannels where the target DNA is bound to the beads. The bead–DNA conjugates are then transferred into a 250 nL PCR reactor for autosomal STR amplification using one biotin and one fluorescence-labeled primer. The resulting biotin-labeled PCR products are electrophoretically injected through a streptavidin-modified capture gel where they are captured to form a concentrated and purified injection plug. The thermally released sample plug is injected into a 14 cm long CE column for fragment separation and detection. The DNA template capture efficiency provided by the on-chip sequence-specific template purification is determined to be 5.4% using K562 standard DNA. This system can produce full 9-plex STR profiles from 2.5 ng input standard DNA and obtain STR profiles from oral swabs in about 3 hours. This fully integrated microsystem with sample-in-answer-out capability is a significant advance in the development of rapid, sensitive, and reliable micro-total analysis systems for on-site human identification.

Graphical abstract: Integrated DNA purification, PCR, sample cleanup, and capillary electrophoresis microchip for forensic human identification

Article information

Article type
Paper
Submitted
27 Oct 2010
Accepted
04 Jan 2011
First published
04 Feb 2011

Lab Chip, 2011,11, 1041-1048

Integrated DNA purification, PCR, sample cleanup, and capillary electrophoresis microchip for forensic human identification

P. Liu, X. Li, S. A. Greenspoon, J. R. Scherer and R. A. Mathies, Lab Chip, 2011, 11, 1041 DOI: 10.1039/C0LC00533A

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