Restriction Digestion and Gel Electrophoresis Laboratory.

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Restriction Digestion and Gel Electrophoresis Laboratory

Transcript of Restriction Digestion and Gel Electrophoresis Laboratory.

Page 1: Restriction Digestion and Gel Electrophoresis Laboratory.

Restriction Digestion and Gel Electrophoresis

Laboratory

Page 2: Restriction Digestion and Gel Electrophoresis Laboratory.

DNA Restriction Enzymes

• Evolved by bacteria to protect against viral DNA infection

• Endonucleases = cleave within DNA strands

• Over 3,000 known enzymes

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Enzyme Site Recognition

• Each enzyme digests (cuts) DNA at a specific sequence = restriction site

• Enzymes recognize 4- or 6- base pair, palindromic sequences (eg GAATTC)

Palindrome

Restriction site

Fragment 1 Fragment 2

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5 vs 3 Prime Overhang

Generates 5 prime overhang Enzyme cuts

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Common Restriction Enzymes

EcoRI– Eschericha coli– 5 prime overhang

Pstl– Providencia stuartii– 3 prime overhang

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The DNA Digestion Reaction

• Restriction Buffer provides optimal conditions– NaCI provides the correct ionic strength– Tris-HCI provides the proper pH– Mg2+ is an enzyme co-factor

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DNA DigestionTemperature

Why incubate at 37°C?– Body temperature is optimal for these and

most other enzymes

What happens if the temperature is too hot or cool? – Too hot = enzyme may be denatured – Too cool = enzyme activity lowered,

requiring longer digestion time

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Restriction Fragment Length PolymorphismRFLP

Allele 1

Allele 2

GAATTCGTTAAC

GAATTCGTTAAC

CTGCAGGAGCTC

CGGCAGGCGCTC

PstI EcoRI

1 2 3

3Fragment 1+2Different Base PairsNo restriction site

M A-1 A-2

Electrophoresis of restriction fragments

M: MarkerA-1: Allele 1 FragmentsA-2: Allele 2 Fragments

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Agarose Electrophoresis Loading

• Electrical current carries negatively-charged DNA through gel towards positive (red) electrode

Power Supply

Buffer

Dyes

Agarose gel

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AgaroseElectrophoresis

Running • Agarose gel sieves DNA

fragments according to size

–Small fragments move farther than large fragments

Power Supply

Gel running

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Analysis of Stained Gel

Determine restriction fragment sizes

–Create standard curve using DNA marker

–Measure distance traveled by restriction fragments

–Determine size of DNA fragments

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• Can be used to determine relative size of a DNA fragment (e.g. size of a gene)

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Molecular Weight Determination

Size (bp) Distance (mm)

23,000 11.0 9,400 13.0

6,500 15.0

4,400 18.0

2,300 23.0

2,000 24.0

100

1,000

10,000

100,000

0 5 10 15 20 25 30

Distance, mm

Siz

e, b

ase

pai

rs

B

A

Fingerprinting Standard Curve: Semi-log

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Equipment

Micropipet—measures small volumes of liquid (l –ml)

1000 l = 1 ml

Microfuge tubes

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Minicentrifuge—pools liquid, solids to bottom of centrifuge tube

Samples of balanced rotor configurations

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Agarose gel--porous