Document Type

Dissertation

Degree

Doctor of Philosophy (PhD)

Major/Program

Chemistry

First Advisor's Name

Bruce McCord

First Advisor's Committee Title

Committee Chair

Second Advisor's Name

Watson Lees

Second Advisor's Committee Title

Committee Member

Third Advisor's Name

Fenfei Leng

Third Advisor's Committee Title

Committee Member

Fourth Advisor's Name

Yuan Liu

Fourth Advisor's Committee Title

Committee Member

Fifth Advisor's Name

DeEtta Mills

Fifth Advisor's Committee Title

Committee Member

Sixth Advisor's Name

George Duncan

Sixth Advisor's Committee Title

Committee Member

Keywords

Chemistry

Date of Defense

3-27-2018

Abstract

There are many situations in forensic DNA typing where the time it takes to identify an individual is critical. Examples include suspects under arrest and individuals detained at ports of entry. It is also important to identify victims quickly when dealing with mass disasters such as terrorist attacks, airplane crashes and natural disasters in order to notify families. The goal of this project was to develop an ultrafast method for screening saliva samples through the use of rapid direct PCR coupled to microfluidic separation and detection.

Fast amplification was achieved through the use of high speed thermocyclers and the experimental optimization of PCR reactants and polymerases. High processivity mutant polymerases were tested at increased speeds along with PCR enhancers. Experimental optimizations and designs were used to ultimately achieve amplification of a 4 loci Y-STR multiplex in 12.5 minutes and a 7 loci STR multiplex in 6.5 minutes.

The use of direct PCR not only decreases the overall time of sample processing through the elimination of the extraction, but also, by the removal of the extraction step cuts down on the possibility of contamination to the sample. By using inhibitor resistant fast polymerases such as Omnitaq, BSA and the PEC-1 enhancer, and optimizing cycling conditions, a direct PCR method was developed where amplification from diluted saliva was successfully achieved in 13.5 minutes.

The products from these ultrafast amplifications can be coupled to a microfluidic chip for analysis. The electrophoretic system separates the PCR products and provides complete genotypes for both Y and autosomal STR multiplexes in 80 seconds. This permits complete sample processing in under 15 minutes for the rapid direct PCR protocol. This screening method can exclude individuals who do not match evidentiary material and test evidence to see if it is be viable for full analysis. The result of this work was a reliable and robust method for the rapid genotyping of forensic samples which can be used in situations where rapid single sample DNA analysis is necessary.

Identifier

FIDC004071

Available for download on Thursday, February 20, 2020

Included in

Chemistry Commons

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