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POLYMERASE CHAIN REACTION. Disclaimer b b This workforce solution was funded by a grant awarded under the President’s Community-Based Job Training Grants.

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Presentation on theme: "POLYMERASE CHAIN REACTION. Disclaimer b b This workforce solution was funded by a grant awarded under the President’s Community-Based Job Training Grants."— Presentation transcript:

1 POLYMERASE CHAIN REACTION

2 Disclaimer b b This workforce solution was funded by a grant awarded under the President’s Community-Based Job Training Grants as implemented by the U.S. Department of Labor’s Employment and Training Administration. The solution was created by the grantee and does not necessarily reflect the official position of the U.S. Department of Labor. The Department of Labor makes no guarantees, warranties, or assurances of any kind, express or implied, with respect to such information, including any information on linked sites and including, but not limited to, accuracy of the information or its completeness, timeliness, usefulness, adequacy, continued availability, or ownership. This solution is copyrighted by the institution that created it. Internal use by an organization and/or personal use by an individual for non-commercial purposes is permissible. All other uses require the prior authorization of the copyright owner.

3 Objectives b Review DNA structure and function b Discuss principle of PCR b Discover advantages and drawbacks to PCR b Determine clinical uses for PCR

4 A quick review of DNA b DNA is composed of four nucleotide bases that pair in a predictable pattern. b DNA is a double stranded molecule that forms a double helix. b DNA strands are held together by hydrogen bonds and van der Waals forces. b Strands of DNA run antiparallel to one another with bases on the interior and a phosphate sugar backbone exterior.

5 DNA Structure

6 PCR: Where did it come from? b First developed in mid-1980’s from an idea by Kary Mullis. b Unveiled to the public in 1985. b Gained widespread popularity in research circles by 1991. b Mullis received the Nobel Prize for Chemistry in 1993.

7 What is the principle of PCR? b PCR can amplify up to billions of copies of a segment of interest. b PCR takes advantage of DNA’s natural replication process. b The polymerase chain reaction has three basic parts.

8 PCR requires several components b Primers comple- mentary to the flanking sequences of the segment of interest b Deoxynucleotide triphosphates (dNTPs). b Template DNA b Taq DNA polymerase b Buffer b A source of Mg 2+ b ddH 2 O b A thermal cycler, or equivalent

9 How does it work? b DS template DNA must be denatured. b Primers hybridize, or anneal to the template DNA. b dNTPs are incorporated into the growing strand. b Target DNA is amplified exponentially.

10 Benefits of PCR b b The ability to amplify target DNA from very minute quantities. b b Rapid identification of microorganisms that are difficult or impossible to isolate in culture. b Early diagnosis of hereditary/genetic disorders or predisposition to them. Earlier diagnosis of infectious diseases that have previously relied on immunologic techniques. b Detection of a single gene mutation.

11 Drawbacks to PCR b PCR reaction mixtures can be easily contaminated. b Some consumables used in the process can be expensive. b Requires the use of special equipment. b Users may need new/refresher training.

12 Clinical Uses of PCR b Early detection of HIV b Identification of M. tuberculosis without culture b Detection of bacterial DNA in middle ear fluid of children b Lyme disease diagnosis from joint fluid b Gonorrhea, Herpes, and Chlamydia detection from genital swab b Rapid detection of Helicobacter pylori b Rapid detection of MRSA


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