Transcript Lab Techniques James Chappell & Cheuk Ka Tong Contents Page 1. Restriction Enzymes 2. Gel Electrophoresis 3. Blotting techniques-Southern, Northern and Western 4. DNA sequencing 5. Polymerase Chain Reaction (PCR) 6. Recombinant DNA 7. Gene.

Lab Techniques
James Chappell & Cheuk Ka Tong
Contents Page
1.
Restriction Enzymes
2.
Gel Electrophoresis
3.
Blotting techniques-Southern, Northern and Western
4.
DNA sequencing
5.
Polymerase Chain Reaction (PCR)
6.
Recombinant DNA
7.
Gene Cloning
8.
References/ Recommended Reading
Restriction Enzymes
• Restriction Nuclease - An enzyme that cleaves a
molecule of DNA at any site where a specific short
sequence of nucleotides occurs.
2key types
• Endonuclease- Cleaves within the DNA molecule
• Exonuclease- Cleaves at the ends of the DNA
molecule
Endonucleases
• 4 types - classified on subunit composition, cleavage
position, sequence-specify and co-factor requirement.
• Type II is the main one that is used in gene cloning.
Two key terms
• Recognition sites – Nucleotide sequence that is
recognised.
• Cleavage sites- Phosphodiester bond that is cleaved.
Endonucleases
• Make break the phosphodiester bond of each of the
stands of the double helix.
5’----GAATTC----3’
3’----CTTAAG----5’
5’----G-3’ 5’AATTC----3’
3’----CTTAA--5’
3’G----5’
EndonucleasesRecognition site + Cleavage site
EndonucleasesRecognition site
3 Considerations•Sequence – Determine specificity
•Length of sequence- Determines frequency
•Palindrome- sequence that reads the same backwards
and forwards.
•Isoshizomers – Restriction enzymes that recognise the
same recognition site
EndonucleasesCleavage site
Endonucleases
Applications
• Allow specific cutting and removal of genes from a complex
molecule of DNA.
• Complementary sticky ends (cohesive ends) allow joining of DNA
molecules.
"The work on restriction nucleases not only permits us easily to
construct recombinant DNA Molecules and to analyze individual
genes but also has led us into the new era of synthetic biology
where not only existing genes are described and analyzed but also
new gene arrangements can be constructed and evaluated"
‘Nobel prizes and restriction enzymes’ in GENE (1971)
Gel Electrophoresis
•
Electrophoresis - the migration of charged molecules
in an electric field though a solution or solid support
•
Various types – defined by support used
1. Paper – amino acids, small peptides
2. Polyacrylamide – Proteins, small DNA/RNA (<500bp)
3. Agarose – DNA/RNA
•
Good preparative and analytical method
Gel Electrophoresis
•
Gel electrophoresis uses a cross-linked polymers
(agarose) that contain various pores.
•
Pores allow molecular sieving, where molecules e.g.
DNA, can be separated based upon there mobility
through the gel.
DNA Gel Electrophoresis
Mobility = Charge + Molecular Dimensions
• Charge per nucleic acid is constant
•This means separation is based upon length of the DNA
molecules and this is how we can separate and identify
DNA molecules.
DNA Gel Electrophoresis
• Linear DNA has a linear relationship to distance
migration.
• If add molecular markers of known mass can calculate
mass of our fragment by plotting a linear plot.
DNA Gel Electrophoresis
•
1.
2.
3.
Other factors determining mobilityPolymer concentration e.g. Agarose
Conformation of DNA
Electrophoresis
DNA Gel Electrophoresis
•
1.
2.
3.
Detection
Dye e.g. ethidium bromide
Audioradiography 32P,
Blotting (see later)
•
1.
2.
Uses
Analytical- Can determine size of DNA fragment,
Preparative – Can identify a specific fragment based
on size
Blotting Techniques
• Blotting – Transfer of DNA, RNA or Proteins, typically
from a electrophoresis gel to a membrane e.g.
nitrocellulose. This membrane can then be subject to
further techniques such as hybridization.
• Hybridization – Process where two complementary
single strands of nucleic acid (DNA or RNA) form a
double helix.
Blotting Techniques
•
•
1.
2.
3.
Using specific probes that are labelled specific sequences of DNA
can be identified.
There are three main hybridization techniques which vary in the
sample blotted and the probes used;
Northern Blot-Transfer of an RNA sample separated and identified
using DNA or RNA probes.
Southern Blot-Transfer of an DNA sample separated and
identified using DNA or RNA probes.
Western Blot- Transfer of an Protein sample separated and
identified typically using an antibody.
Applications
• The main use of this technique is to identity any changes in DNA
sequencing or genes expressed, e.g. comparing genes expressed
by a diseased cell to genes expressed by an healthy cell.
• Other uses include- Testing for hereditary disease, Evolutionary
history of species, Screening e.g.food supply
• Applications to synthetic biology
- identification of various parts in natural organisms,
-?more?
DNA Sequencing
• DNA Sequencing – Determining the order of nucleotides in a DNA
molecule
• Key technique as it can give us information about a DNA molecule,
e.g. location and order of genes, restriction sites.
• In addition, for recombinant DNA gives verification of gene cloning
experiments.
• 2 possible use’s for project – Identify sequence of new part,
- Checking recombinant DNA.
• Various techniques are available.
• The key technique used today is Dideoxy method.
DNA Sequencing
Deoxyribonucleotide acid
This is essentially the monomer of
DNA. Polymerization of nucleotides
occurs by condensation reaction of a
5’ phosphate to a 3’ hydroxyl group
Dideoxyribonucleotide acid
There is no 3’hydroxyl group to
allow polymerization.
Polymerase Chain Reaction (PCR)
•
A method for amplifying specific DNA sequences.
•
Components required:
- Target sequence
- A pair of primers
- dNTPs (ATGC)
- DNA polymerase
PCR
• One PCR cycle involves three steps:
- Strand separation (95ºC)
- Hybridization of primers (54ºC)
- DNA synthesis (72ºC)
• After n cycles, the sequence is
amplified 2n-fold.
Polymerase Chain Reaction (PCR)
•
Five noteworthy features of PCR:
1)
The sequence of the target need not be known.
2)
The target can be much larger than the primers (>10 kb).
3)
Primers do not have to perfectly match flanking sequences.
4)
Stringency can be controlled by temperature and salt (MgCl2).
5)
PCR is very sensitive.
Recombinant DNA Technology
• The construction of new combinations of unrelated
genes.
• These novel combinations can be cloned and amplified
by introducing them into host cells.
Recombinant DNA Technology
• A DNA fragment of interest is covalently joined to a DNA
vector.
- A vector can replicate autonomously in an appropriate
host.
- Plasmids and phage λ are common vectors for cloning
in E.coli.
Recombinant DNA Technology
• The DNA fragment of interest
and the plasmid vector are
both cut using the same
restriction enzyme.
• The single-stranded ends of
the fragment are
complementary to those of the
cut plasmid.
• The DNA fragment and the cut
plasmid are annealed and then
joined by DNA ligase.
Gene Cloning
• One of the most useful plasmids for cloning is pBR322.
• pBR322 contains genes for resistance to tetracycline
and ampicillin.
• Different endonucleases can cleave this plasmid at a
variety of unique sites.
Gene Cloning
• Insertion of DNA at the
EcoRI site does not alter
either of the genes for
antibiotic resistance.
• However insertion at the
SalI or PstI site causes
insertional inactivation.
 Basis for selection of
cells containing
recombinant DNA.
References/
Recommended Readings
1.
Chapter 8 – Manipulating Proteins, DNA and RNA
- Molecular Biology of the Cell (4th Edition), Alberts, Johnson, Lewis, Raff,
Roberts, Walter, Garland Science
2.
Chapter 6- Exploring Genes
-Biochemistry (5th Edition), Berg, Tymoczko, Stryer, Freeman