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Chapter 3 (Part 2) : Protein Purification and Analysis

This document discusses protein purification and analysis. It describes why proteins must be purified, including for studying enzyme function and structural analysis. The main steps of protein purification are developing an assay, choosing a protein source, preparing a tissue extract through cell disruption and fractionation, and using multiple protein fractionation techniques. Key techniques mentioned are differential centrifugation to separate cell components and organelles, and various types of chromatography to further purify the protein, such as gel permeation, ion-exchange, and affinity chromatography. Additional analytical techniques are also summarized, such as SDS-PAGE electrophoresis to determine protein size and purity, isoelectric focusing by pH, amino acid analysis, protein sequencing, proteolytic digestion, and mass spectrometry.

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69 views

Chapter 3 (Part 2) : Protein Purification and Analysis

This document discusses protein purification and analysis. It describes why proteins must be purified, including for studying enzyme function and structural analysis. The main steps of protein purification are developing an assay, choosing a protein source, preparing a tissue extract through cell disruption and fractionation, and using multiple protein fractionation techniques. Key techniques mentioned are differential centrifugation to separate cell components and organelles, and various types of chromatography to further purify the protein, such as gel permeation, ion-exchange, and affinity chromatography. Additional analytical techniques are also summarized, such as SDS-PAGE electrophoresis to determine protein size and purity, isoelectric focusing by pH, amino acid analysis, protein sequencing, proteolytic digestion, and mass spectrometry.

Uploaded by

simayyilmaz
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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Chapter 3 (part 2)

Protein purification and Analysis


Why purify proteins?
Pure proteins are required to study enzyme
function
Pure proteins are required for structural
analysis (x-ray crystallography, NMR
spectroscopy)
Pure proteins are required to obtain amino
acid sequence
Steps in protein purification
Develop assay
Choose source of protein
Prepare tissue extract
cell disruption
subcellular fractionation
Protein fractionation (several steps)
Determination of purity
Differential Centrifugation
tissue
homogenate
1000 g
Pellet
unbroken cells
nuclei
chloroplast
transfer
supernatant
transfer
supernatant
transfer
supernatant
10,000 g 100,000 g
Pellet
mitochondria
Pellet
microsomal
Fraction
(ER, golgi,
lysosomes,
peroxisomes)
Super.
Cytosol,
Soluble
enzymes
Chromatography
Gel Permeation
Chromatography
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Cl
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low salt buffer high salt buffer
Ion-exchange
Chromatography
Affinity Chromatography
Add excess ligand
SDS poly acrylamide electrophoresis (PAGE)
SDS = H
3
C-(CH
2
)
10
-CH
2
-OSO
3
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SDS denatures protein
coats w/ negative charge
Used to determine protein MW
And purity of protein prep
Isoelectric Focusing
D
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p
H
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p
H
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pH 9
pH 3
2-D Electrophoresis
D
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s
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g

M
W
small
large
Decreasing pH
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SDS-PAGE
Decreasing pH
D
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M
W
Amino Acid Analysis
H
3
N
C
H
C
O
R
O
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N C S
N
C
S
HN
C
C
H
O
R
1) Acid hydrolyze protein
2) Treat with phenylisothiocyanate (PICT)
3) Separate derivatized AAs by HPLC
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Protein Sequencing
(Edman Degradation)
N C S
H
3
N
C
H
C
O
R
NH C
H
C
O
R
X
N C
S
HN
C
H
C
O
R
NH C
H
C
O
R
X
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Trifluoroacetic acid
N
C
S
HN
C
C
H
O
R
2HN C
H
C
O
R
X
1)
2)
3)
R
e
p
e
a
t
Can sequence in 30 to 60 AAs from N-terminus
Generate Proteolytic
Fragments
Endopeptidases
Typsin cleaves at COOH end of Lys and Arg
Chymotrypsin cleaves at COOH end of Phe, Tyr, Trp
Chemical Cleavages
Cyanogen Bromide cleaves at COOH end of Met
Generate overlapping fragments
Sequence individual fragments and piece together sequence
Peptide mapping exercise
Met-Ala-Arg- Gly-Glu-Tyr-Met-Cys-Lys-Phe-Ala-Glu-Gln-Asp
Trypsin
Met-Ala-Arg
Phe-Ala-Glu-Gln-Asp
Gly-Glu-Tyr-Met-Cys-Lys
Chymotrysin
Met-Ala-Arg- Gly-Glu-Tyr
Met-Cys-Lys Phe
Ala-Glu-Gln-Asp
CNBr
Met
Ala-Arg-Gly-Glu-Tyr-Met
Cys-Lys-Phe-Ala-Glu-Gln-Asp
Proteomic Analysis
Matrix Assisted Laser Desorption Ionization Time of Flight
(MALDI-TOF)

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