色層分析法 chromatography 3.1 色層分析原理juang.bst.ntu.edu.tw/files ecx/2005...
TRANSCRIPT
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3 Chromatography
3.1 Basic principles
3.2 Gel filtration
3.3 Ion exchange
3.4 Affinity chromatography
3.5 HPLC FPLC
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Historical review
Round filter paper
Long rectangle paper
Thin layer(TLC)
Column
Samplecapacity increased
Largercapacity
Development
Adapted from Scope RK (1987) Protein Purification Principles and Practice p.9
Paper partition chromatography (PPC)
Martin, Synge (1952)
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Essential mechanism
Polar PolarNon-polar Non-polar
LikeDissolves
Like
LikeDissolves
Like
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LL
Two-phase separation system
Mobilephase
Stationaryphase
ADSORPTION PARTITIONLiquid - Solid Liquid - Liquid
Two-phaseA B C
One Plate ofSeparationTheoretical
platenumber
SPolar
L
Non-Polar
PolarNon-polar
Sample Sample
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One plate
One separation, one plate
B
B BB B
B B BB
BBA
A
AAA
A
A
A
AA
AA
AA
AA
AA
AA
B
B BB BB B
B
B
B
80
20
10
90
6416
19
164
981
5113
01
31
873Polar
Non-polar
100A+
100B
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Common chromatographic methods
Gel filtrationReverse phase
chromatography
Ion exchangeAffinity
chromatographyHydrophobic
interactionHydroxyapatite
AdsorptionPartition
PPC, TLC, GC TLC, GCSmall
molecules
Largemolecules
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Thin-layer chromatography
Thin-layer plate
Sample spotting Add developer Developing
ActivatedActivated
NotNot--activatedactivated
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3.2 Gel filtration
3.2.1 Basic principles partition
3.2.2 Gel materials
3.2.3 Gel and column
3.2.4 Column operation
3.2.5 Problem and solution
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Smaller molecules are retarded
Largermolecules
Small molecules
Partition
Sample
Stationary phase
Mobilephase
Stokes radiusMolecular sizeand shape
Elute out fasterGel filtration is a partition type chromatography Juang RH (2005) EPA
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Pharmacia
Bio-Rad
SephadexSepharoseSephacrylSephacel
BioGel PBioGel A
glucose (dextrose)agaroseglucose + acrylamidecellulose
acrylamideagarose
FPLC Superose, SuperdexMono Q, Mono S
Gel material is a polymer of carbohydrate or acrylamide Juang RH (2005) EPA
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Pha
rmac
ia (1
991)
Gil
Filtr
atio
n
Prin
cipl
es a
nd M
etho
ds p
.35
Sephadex
glucose unit
Space for filtration
Sephadex is the polymer of glucose with chemical cross-linking
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Sephadex G
MW ranged from ten to several hundred thousands
Pharmacia (1991) Gil Filtration Principles and Methods p.37
G-200 could be smashed flat easily
From powder to gel form1 g 20 mL gel1 g 7.5 mL
(its backbone support is too weak)
Small proteins
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Pha
rmac
ia (1
991)
Gil
Filtr
atio
n
Prin
cipl
es a
nd M
etho
ds p
.22
Sephacryl
AcrylamideCross-linking
Bigger spaceStronger support for backbone
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Agar gel formation
Pharmacia (1991) Gil Filtration Principles and Methods p.38, 39
Even stronger backboneMuch bigger space
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Sepharose
MW ranged from ten thousands to several millions
Pharmacia (1991) Gil Filtration Principles and Methods p.40
2% gel6% gel
Large proteins
Sepharose is rigid
Sephadex
Sephacry
Cross-linking
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Gel filtration beads
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Spaces in a column
Adapted from Pharmacia (1991) Gil Filtration Principles and Methods p.11
Vt Vo Vt - Vo
Mobile phase Stationary phase
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A typical chromatogram
XY
ZEnzymeactivity NaCl
Vo
Vt
(E) (Y)
Elution Volume (mL)
A
VoVe
Vt0
E
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Poor separationPeak flattened
Best separation
0
50
100
0.5 1.0 1.5
Superfine
Fine
Corse
Ve/Vt
0
50
100
0
50
100Rel
ativ
e am
ount
Ada
pted
from
Pha
rmac
ia: G
il Fi
ltrat
ion
P
rinci
ples
and
Met
hods
Bead size is critical to the resolution of gel chromatography
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Dispersion
Diffuse in and out bead
Sample or buffer is diffusing in and then out of the gel particle.
DiffusionJuang RH (2005) EPA
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Two types of gel
Dispersion ()
Small particle size reduces the diffusion time and increases the resolution of the gel
Dispersion type gels let the sample molecules flow directly through the gel body, and have better resolution
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Bead size vs flow rate
Adapted from Scope RK (1987) Protein Purification Principles and Practice p.192
Smaller particles also reduce the space between the beads, and prevent the turbulence as the buffer flows, but the flow rate might be decreased
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Sephacryl S-200
Elution volume
Sephacryl S-300
Ads
orba
nce
Ada
pted
from
Pha
rmac
ia: G
il Fi
ltrat
ion
P
rinci
ples
and
Met
hods
0
50
100
0
50
100
Choose the gel which brings your target protein out of the column earlier
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Sample volume at 1% of Vt
Sample volume at 1~2% of total gel volume
Adapted from Pharmacia (1991) Gil Filtration Principles and Methods p.46
Superdex 200Transferrin (81 kD)& IgG (160 kD)
0 1 2 3 4 5
0.5
1.0
1.5
Sample volume (% of Vt)
Resolution
a
cb
R = a(b+c)/2
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Ada
pted
from
Pha
rmac
ia (1
991)
Gil
Filtr
atio
n
Prin
cipl
es a
nd M
etho
ds p
.59
Elution time (h)
Con
cent
ratio
n
Bed height (cm)
Flow rate (mL/cm2/h)
85
85
20
2
25
25
0 1 2 3
0 10 20 30Increaseflow rate
Reducecolumn height
A B C
A B C
AB C
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10 cm2
30 cm
10 cm
30 cm2
300 cm3
Short and fat
Long and slim
Fat column cannot tolerate poor separation
But it has better flow rate and higher capacity
Adapted from Scope RK (1987) Protein Purification Principles and Practice p.195
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A
Buffer
Gradient mixer
Pump
Recorder
Monitor
Column
Gel
Fraction collector
(1)
(2)
(3) (4)
(5)
adapter
reservoir
Connector
The whole family of liquid chromatography apparatus Juang RH (2005) EPA
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Packing column step by step
Equilibratedin buffer
Temperatureequilibrated
Gel stands o/n
Wash gel well
Estimate
gel volume Pouring gelsmoothly
Stop elution X
Keep eluting
Put on reservoir
Sediment
In progressing
Supernatant
Elute under
High pressure
Put on adaptor
12 Gel
GelCheck flow rate of empty column
Gel should be packed tightlyJuang RH (2005) EPA
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Packing column
Pour gel slurry smoothly (non-stop), avoid trapping any bubble Ph
arm
acia
(199
1) G
il Fi
ltrat
ion
P
rinci
ples
and
Met
hods
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General principle for column chromatography
Gel selection Make target protein elute out column earlier
Bead size Finer bead has better resolution, slower flow rate
Column size Use larger column size but consider practical need
Flow rate Fast flow reduces resolution, slow
Sample volume Apply 1% of total gel volume for sample
Column shape Slim column for gel filtration, fat column for others
Pack tightly Pack the gel tightly for better resolution
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