pcr application & techniques

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Latest -PCR APPLICATION by A.Arputha Selvaraj

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Page 1: PCR APPLICATION & TECHNIQUES

Latest -PCR APPLICATION

by

A.Arputha Selvaraj

Page 2: PCR APPLICATION & TECHNIQUES

What is PCR?What is PCR?

It was invented in 1983 by Dr. Kary Mullis, for which he received the Nobel Prize in Chemistry in 1993.

PCR is an exponentially progressing synthesis of the defined target DNA sequences in vitro.

Page 3: PCR APPLICATION & TECHNIQUES

What is PCR? : What is PCR? : Why “Polymerase”?Why “Polymerase”?

It is called “polymerase” because the only enzyme used in this reaction is DNA polymerase.

Page 4: PCR APPLICATION & TECHNIQUES

What is PCR? : What is PCR? : Why “Chain”?Why “Chain”?

It is called “chain” because the products of the first reaction become substrates of the following one, and so on.

Page 5: PCR APPLICATION & TECHNIQUES

What is PCR? : What is PCR? : The “Reaction” ComponentsThe “Reaction” Components

1) Target DNA - contains the sequence to be amplified.

2) Pair of Primers - oligonucleotides that define the sequence to be amplified.

3) dNTPs - deoxynucleotidetriphosphates: DNA building blocks.

4) Thermostable DNA Polymerase - enzyme that catalyzes the reaction

5) Mg++ ions - cofactor of the enzyme

6) Buffer solution – maintains pH and ionic strength of the reaction solution suitable for the activity of the enzyme

Page 6: PCR APPLICATION & TECHNIQUES

The ReactionThe Reaction

THERMOCYCLERPCR tube

Page 7: PCR APPLICATION & TECHNIQUES

Denature (heat to 95oC)

Lower temperature to 56oC Anneal with primers

Increase temperature to 72oC DNA polymerase + dNTPs

Page 8: PCR APPLICATION & TECHNIQUES
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DNA copies vs Cycle number

0

500000

1000000

1500000

2000000

2500000

0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23

Cycle number

DN

A c

op

ies

Page 11: PCR APPLICATION & TECHNIQUES

Applications of PCRApplications of PCR

• Classification of organisms

• Genotyping• Molecular archaeology

• Mutagenesis• Mutation detection• Sequencing• Cancer research

• Detection of pathogens

• DNA fingerprinting

• Drug discovery• Genetic matching• Genetic engineering

• Pre-natal diagnosis

Page 12: PCR APPLICATION & TECHNIQUES

Applications of PCR

Basic Research Applied Research• Genetic matching

• Detection of pathogens

• Pre-natal diagnosis

• DNA fingerprinting

• Gene therapy

• Mutation screening

• Drug discovery

• Classification of organisms

• Genotyping

• Molecular Archaeology

• Molecular Epidemiology

• Molecular Ecology

• Bioinformatics

• Genomic cloning

• Site-directed mutagenesis

• Gene expression studies

Page 13: PCR APPLICATION & TECHNIQUES

Applications of PCR

Molecular Identification Sequencing Genetic Engineering

• Molecular Archaeology

• Molecular Epidemiology

• Molecular Ecology

• DNA fingerprinting

• Classification of organisms

• Genotyping

• Pre-natal diagnosis

• Mutation screening

• Drug discovery

• Genetic matching

• Detection of pathogens

• Bioinformatics

• Genomic cloning

• Human Genome Project

• Site-directed mutagenesis

• Gene expression studies

Page 14: PCR APPLICATION & TECHNIQUES

MMOLECULAROLECULAR IIDENTIFICATION:DENTIFICATION:

Page 15: PCR APPLICATION & TECHNIQUES
Page 16: PCR APPLICATION & TECHNIQUES

Detection of Unknown MutationsDetection of Unknown MutationsMolecular Identification:

Page 17: PCR APPLICATION & TECHNIQUES

SSCP gels: “shifts” representing a mutation in the amplified DNA fragment

Page 18: PCR APPLICATION & TECHNIQUES

Classification of OrganismsClassification of Organisms

1) Relating to each other

2) Similarities

3) Differences

* Fossils

* Trace amounts

* Small organisms

! DNA !

Molecular Identification:

Insufficient data

Page 19: PCR APPLICATION & TECHNIQUES
Page 20: PCR APPLICATION & TECHNIQUES

Rademaker et al. 2001

Page 21: PCR APPLICATION & TECHNIQUES

Detection Of PathogensDetection Of Pathogens

Molecular Identification:

Page 22: PCR APPLICATION & TECHNIQUES

Detection Of PathogensDetection Of Pathogens

Sensitivity of detection of PCR-amplified M. tuberculosis DNA. (Kaul et al.1994)

Molecular Identification:

Page 23: PCR APPLICATION & TECHNIQUES

Sensitivity of detection of PCR-amplified M. tuberculosis DNA. (Kaul et al.1994)

Page 24: PCR APPLICATION & TECHNIQUES

GenotypingGenotyping by STR markers by STR markers

Molecular Identification:

Page 25: PCR APPLICATION & TECHNIQUES

Prenatal DiagnosisPrenatal Diagnosis

644 bp

440 bp

204 bp

Molecular analysis of a family with an autosomal recessive disease.

Molecular Identification:

• Chorionic Villus

• Amniotic Fluid

Page 26: PCR APPLICATION & TECHNIQUES

SSEQUENCINGEQUENCING

Nucleotides (dNTP) are modified (dideoxynucleotides = ddNTP)

NO polymerisation after a dideoxynucleotide!

Fragments of DNA differing only by one nucleotide are generated

Nucleotides are either or

Page 27: PCR APPLICATION & TECHNIQUES
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Classical Sequencing GelClassical Sequencing Gel

Sequencing:

Page 29: PCR APPLICATION & TECHNIQUES

Reading Classical Sequencing GelsReading Classical Sequencing Gels

Sequencing:

Page 30: PCR APPLICATION & TECHNIQUES

Sequencing:

Page 31: PCR APPLICATION & TECHNIQUES

SummarySummary

blood, chorionic villus, amniotic fluid, semen, hair root, saliva

68,719,476,736 copies Gel Analysis, Restriction Digestion, Sequencing

Page 32: PCR APPLICATION & TECHNIQUES

ConclusionConclusion

The speedspeed and easeease of use, sensitivitysensitivity, specificityspecificity and

robustnessrobustness of PCR has revolutionised molecular biology

and made PCR the most widely used and powerful

technique with great spectrum of research and

diagnostic applications.

Page 33: PCR APPLICATION & TECHNIQUES

Thank You