CH339K Proteins: Primary Structure, Purification, and Sequencing.
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Transcript of CH339K Proteins: Primary Structure, Purification, and Sequencing.
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CH339K
Proteins: Primary Structure, Purification, and Sequencing
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-Amino Acid-Amino Acid
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•All amino acids as incorporated are in the L-formAll amino acids as incorporated are in the L-form• Some amino acids can be changed to D- after Some amino acids can be changed to D- after incorporationincorporation• D-amino acids occur in some non-protein moleculesD-amino acids occur in some non-protein molecules
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C
HOOC
NH2
R H C
HOOC
NH2
RH
L-amino acid D-amino acid
I prefer this layout, personally…
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2 Amides
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The Acidic and the Amide Amino Acids Exist as Conjugate Pairs
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Ionizable Side Chains
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Hydrogen Bond Donors / Acceptors
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Disulfide formation
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4-Hydroxyproline Collagen
5-Hydroxylysine Collagen
6-N-Methyllysine Histones
-Carboxygultamate Clotting factors
Desmosine Elastin
Selenocysteine Several enzymes (e.g. glutathione peroxidase)
Modified Amino AcidsModified Amino Acids
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A Modified Amino Acid That Can Kill You
Diphthamide (2-Amino-3-[2-(3-carbamoyl-3-trimethylammonio-propyl)-3H-imidazol-4-yl]propanoate)
Histidine
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• Diphthamide is a modified Histidine residue in Eukaryotic Elongation Factor 2
• EF-2 is required for the translocation step in protein synthesis
Diphthamide Continued – Elongation Factor 2
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Corynebacterium diphtheriaeCorynebacterium diphtheriae CorynebacteriophageCorynebacteriophage
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Diphtheria Toxin Action
• Virus infects bacterium• Infected bacxterium
produces toxin• Toxin binds receptor on
cell• Receptor-toxin complex
is endocytosed• Endocytic vessel
becomes acidic• Receptor releases toxin• Toxin escapes
endocytic vessel into cytoplasm
• Bad things happen
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• Diphtheria toxin adds a bulky group to diphthamide
• eEF2 is inactivated• Cell quits making
protein• Cell(s) die• Victim dies
Diphtheria Toxin Action
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Other Amino Acids
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Every Every -amino acid has at -amino acid has at least 2 pKa’sleast 2 pKa’s
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PolymerizationPolymerization
GG00’ = +10-15 kJ/mol’ = +10-15 kJ/mol
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In vivoIn vivo, amino acids are , amino acids are activatedactivated by coupling to by coupling to tRNAtRNA
Polymerization of activated Polymerization of activated a.a.:a.a.:GGoo’ = -15-20 kJ/mol’ = -15-20 kJ/mol
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• In vitro, a starting amino acid In vitro, a starting amino acid can be coupled to a solid matrixcan be coupled to a solid matrix• Another amino acid withAnother amino acid with
• A protected amino groupA protected amino group• An activating group at the An activating group at the carboxy groupcarboxy group
• Can be coupledCan be coupled• This method runs backwards This method runs backwards from in vivo synthesis (Cfrom in vivo synthesis (C N) N)
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Peptide Bond
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Resonance stabilization of peptide bond
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Cis-trans isomerization in prolines
•Other amino acids have a trans-cis ratio of ~ 1000:1Other amino acids have a trans-cis ratio of ~ 1000:1•Prolines have cis:trans ratio of ~ 3:1Prolines have cis:trans ratio of ~ 3:1•Ring structure of proline minimizes Ring structure of proline minimizes GG00 difference difference
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Physical Methodsor
How to Purify and Sequence a
Weapons-Grade Protein
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First Question
How do I measure the amount of protein I have?
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UV Absorption Spectrophotometry
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Beer-Lambert Law
clTA
I
IT cl
o
log :Absorbance
elyalternativor
10 :nceTransmitta
c = concentrationc = concentrationl = path lengthl = path length = extinction coefficient= extinction coefficientAn Absorbance = 2 means that only 1% of the incident beam is An Absorbance = 2 means that only 1% of the incident beam is getting through. getting through.
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Transmittance and Absorbance
Absorbance vs. Concentration Transmittance vs. Concentration
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Second Question
How can I spot my protein in the great mass of different proteins?
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Electrophoresis
d
- - -
-
+
-
-
+
ChargedMolecule
(Charge q)
dV
F = qV/d
Gel matrix
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f
q
E
v
qEfv
v
f
fvF
E
q
qEd
VqF
b
f
or
:mequilibriuAt
velocity
tcoefficien frictional
strength field
charge
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f
q
E
v
M
qv
The frictional coefficient The frictional coefficient f f depends on the size of the depends on the size of the molecule, which in turn depends upon the molecular mass, molecule, which in turn depends upon the molecular mass, so:so:
i.e. the velocity depends on the charge/mass ratio, which i.e. the velocity depends on the charge/mass ratio, which varies from protein to proteinvaries from protein to protein
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Polyacrylamide Gels
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Polyacrylamide gel electrophoresis of whole cell proteins of three strains of lactic acid bacteria.
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Agarose
Gelidium sp.Gelidium sp.
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SDS binds to proteins at a constant ratio of 1.4 g SDS/g proteinSDS binds to proteins at a constant ratio of 1.4 g SDS/g protein
Na+
OS
OCH2
CH
2
CH2
O
O
CH
2
CH2
CH
2
CH2
CH
2
CH2
CH
2
CH2
CH3
SDS PAGESodium Dodecyl (Lauryl) Sulfate
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Constant q/M ratioConstant q/M ratio
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rf logM
1 R
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Disulfide cleavage
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Isoelectric Point
Abrin A - Predicted Charge
-40
-30
-20
-10
0
10
20
30
0.0 2.0 4.0 6.0 8.0 10.0 12.0 14.0
pH
Ch
arg
e o
n P
rote
in
Predicted pI5.088
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Isoelectric FocusingIsoelectric Focusing
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pH
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Carrier Ampholytes
• Amphoteric Electrolytes
• Mixture of molecules containing multiple amino- and carboxyl- groups with closely spaced pIs
• Partition into a smooth, buffered pH gradient
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Separation by pISeparation by pI
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Isoelectric Focusing
BelowBelow the pI, a protein has a positive charge and migrates the pI, a protein has a positive charge and migrates toward the cathodetoward the cathodeAboveAbove the pI, a protein has a negative charge and migrates the pI, a protein has a negative charge and migrates toward the anodetoward the anode
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Isoelectric Focusing Foot Flesh Extracts from Pomacea flagellata and Pomacea patula
catemacensis
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STOPHERE
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Protein Purification Steps1 unit = amount of enzyme that catalyzes 1 unit = amount of enzyme that catalyzes conversion of 1 conversion of 1 mol of substrate to product in 1 mol of substrate to product in 1 minuteminute
1 unit = amount of enzyme that catalyzes 1 unit = amount of enzyme that catalyzes conversion of 1 conversion of 1 mol of substrate to product in 1 mol of substrate to product in 1 minuteminute
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Purification visualized
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Example:Purification of Ricin
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Georgi Markov1929-1978
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Ricinus communisRicinus communis – castor oil – castor oil plantplant
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Ricin
Ricin B chainRicin B chain(the attachment bit)(the attachment bit)
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Ricin uptake and release1.1. endocytosis by coated pits and endocytosis by coated pits and
vesicles or, vesicles or, 2.2. endocytosis by smooth pits and endocytosis by smooth pits and
vesicles. The vesicles fuse with an vesicles. The vesicles fuse with an endosome. endosome.
3.3. Many ricin molecules are returned to Many ricin molecules are returned to the cell surface by exocytosis, or the cell surface by exocytosis, or
4.4. the vesicles may fuse to lysosomes the vesicles may fuse to lysosomes where the ricin would be destroyed. where the ricin would be destroyed.
5.5. If the ricin-containing vesicles fuse If the ricin-containing vesicles fuse to the Trans Golgi Network, (TGN), to the Trans Golgi Network, (TGN), there ís still a chance they may there ís still a chance they may
6.6. return to the cell surface. return to the cell surface. 7.7. Toxic action will occur when RTA, Toxic action will occur when RTA,
aided by RTB, penetrates the TGN aided by RTB, penetrates the TGN membrane and is liberated into the membrane and is liberated into the cytosol.cytosol.
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Ricin Action
• Ricin and related enzymes remove an adenine base from the large ribosomal RNA
• Shut down protein synthesis
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The possibility that ricin might be used as an asymmetric warfare weapon has not escaped the attention of the armed services.
The last time I was qualified to know for sure, there were no effective antidotes.
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Significant Terrorist Incidents Involving Chemical and Biological Agents
Year Organization Agents
1946 DIN("Revenge" in Hebrew; also Dahm Y'Israel Nokeam, "Avenging Israel's Blood")(Germany)
Arsenic Compounds
1970 Weather Underground(United States)
Tried to obtain agents from Ft. Detrick by blackmailing a homosexual serviceman.
1972 R.I.S.E (United States)
Typhoid, diphtheria, dysentery, meningitis and several others to be delivered by aerosol.
1974 Aliens of America(Alphabet Bomber)(United States)
Nerve Agents
1980 R.A.F. (Rote Armee Faktion) (Germany)
Botulinum toxin
1984 Rajneshee Cult (United States) Salmonella enterica serovar typhimurium
1991 Minnesota Patriots Council(United States)
Ricin
1990-1995 Aum Shinrikyo(Japan)
Bacteria and viral agents, toxins, organophosphorus nerve agents.
1995 Aryan Nation (United States)
Yersinia pestis
1995 The Covenant and the Sword (United States)
Ricin
1998 Republic of Texas(United States)
Bacterial and viral agents
2001 Unknown (United States) Bacillus anthracis
2003-2004 Fallen Angel (United States) Ricin
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RawExtract
(NH4)2SO4
Cut
Affinity GelFiltration
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Salting In – Salting out
iz
ic
zcI
i
i
n
iii
ion on charge
ion ofion concentrat
2
1 :Strength Ionic
1
2
• salting in: Increasing ionic strength increases protein solubility
• salting out: Increasing further leads to a loss of solubility
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Salting in – salting out
The solubility of haemoglobin in different electrolytes as a function of ionic strength.Derived from original data by Green, A.A. J. Biol. Chem. 1932, 95, 47
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Solubility reaches minimum at pI
Salting in: Counterions help prevent formation of interchain salt links
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Salting out: there’s simply less water available to solubilize the protein.
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Different proteins have different solubilities in (NH4)2SO4
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Lyotropic ChaotropicSeries
Cations: N(CH3)3H+> NH4+> K+> Na+> Li+> Mg2+>Ca2+> Al3+>
guanidinium / urea
Anions: SO42−> HPO4
2−> CH3COO−> citrate > tartrate > F−> Cl−> Br−> I−> NO3
−> ClO4−> SCN−
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1) Bring to 37% Saturation – ricin still soluble, many other proteins ppt
2) Collect supernatant3) Bring to 67% Saturation – ricin ppt, many remaining
proteins still soluble4) Collect pellet5) Redissolve in buffer
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Dialysis and Ultrafiltration(How do you get the %@$&#! salt out?)
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RawExtract
(NH4)2SO4
Cut
Affinity GelFiltration
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Separation by chromatographySeparation by chromatographyBasic Idea:Basic Idea:You have a You have a stationary phasestationary phaseYou have a You have a mobile phasemobile phaseYour material partitions out between Your material partitions out between the phases.the phases.
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Affinity Chromatography
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Structure of AgaroseAgarose is a polymer of agarobiose, which in turn consists of one unit each of galactose and 3,6-anhydro-a-L-galactose.
Ricin sticks to galactose, so store-bought agarose acts as an affinity column right out of the bottle, with ricin binding the beads while other proteins wash through.
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Begin adding 0.2 M Begin adding 0.2 M LactoseLactose
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RawExtract
(NH4)2SO4
Cut
Affinity GelFiltration
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B
AB
BAASS SS
SS
Ricinus communis Agglutinin (RCA)MW = 120,000
RicinMW = 60,000
Castor Beans contain two proteins that bind galactose
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Gel Filtration
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Gel Filtration
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Gel Filtration (aka Size Exclusion)
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VmVm = = matrixmatrix volume volume
VoVo = = voidvoid volume volume
VpVp = = porepore volume volume
VtVt = = totaltotal volume volume
VeVe = = elutionelution volume volume
(1a) Vt = Vo + Vp or(1a) Vt = Vo + Vp or
(1b) Vp = Vt - Vo(1b) Vp = Vt - Vo
(2) Ve = Vo + Kav*Vp(2) Ve = Vo + Kav*Vp
Combining 1b with 2Combining 1b with 2
You knew I couldn’t leave it at that…
0t
oeav VV
VVK
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• a and b represent the effective separation range
• c corresponds to the exclusion limit
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Kav
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Fig. 3. Fig. 3. Measurement of molecular weight of native NAGase enzyme of green crab by gel Measurement of molecular weight of native NAGase enzyme of green crab by gel filtration on Sephadex G-200: standard proteins (empty circles); green crab NAGase filtration on Sephadex G-200: standard proteins (empty circles); green crab NAGase (filled circle). (filled circle).
From Zhang, J.P., Chen, Q.X., Wang, Q., and Xie, J.J. (2006) From Zhang, J.P., Chen, Q.X., Wang, Q., and Xie, J.J. (2006) Biochemistry (Moscow)Biochemistry (Moscow) 7171(Supp. 1) (Supp. 1) 855-859.855-859.
Note:Note: smaller = slowersmaller = slower, , whereas in SDS-PAGE, whereas in SDS-PAGE, smaller = fastersmaller = faster..
NoteNote
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RCARCA
RicinRicin
Gel Filtration Separation of RicinGel Filtration Separation of Ricin
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RawExtract
(NH4)2SO4
Cut
Affinity GelFiltration
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Okay, Now Let’s Sequence the A-Chain
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Bovine InsulinBovine Insulin21 residue A chain21 residue A chain31 residue B chain31 residue B chainConnected by disulfidesConnected by disulfides
In order to sequence the protein, the In order to sequence the protein, the chains have to be separatedchains have to be separated
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Chain Separation
• Interchain disulfide broken by high concentrations of ME
• Chains are about the same size – but can take advantage of different pIs– B-Chain pI ~ 5.3– A-Chain pI ~ 7.2
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Ion Exchangers
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•Apply ME – treated ricin to DEAE-cellulose at pH 7•At pH 7:
•A chain (pKa 7.2) is essentially uncharged, •B chain (pKa 4.8) is highly negative
•A chain washes through the column•B chain sticks, eluted with gradient of NaCl
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2-D Electrophoresis (an aside)
• Can use two different properties of a protein to separate electrophoretically
• For analysis of cellular protein content, often use 2-dimensional electrophoresis:
• 1st dimension is isoelectric focusing
• 2nd dimension is SDS PAGE
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2-D Electrophoresis (cont.)
• Can use other protein properties to separate– Simple PAGE at 2 different pHs– PAGE and SDS PAGE
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Sequencing with Phenylisothiocyanate
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• Applied Biosystems 492 Procise Protein Sequencer
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Chain Cleavage: Cyanogen Bromide
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C-Terminal Sequencing
• Carboxypeptidases are enzymes that chew proteins from the carboxy terminus
• Can incubate a protein (preferably denatured – more later) with a carboxypeptidase
• Remove aliquot at intervals (time course)
• Run amino acid analysis of aliquots
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C-Terminal Sequencing of Rat Plasma Selenoprotein
From Himeno et al (1996) J. Biol. Chem. From Himeno et al (1996) J. Biol. Chem. 271271: 15769-15775.: 15769-15775.
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Tandem Mass Spectrometry can also be used to determine peptide sequences
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MOLECULAR EVOLUTION
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Time of Divergence|-------------|-------------|------------|------------|-------------|------------| ┌───────────────────────────────Shark │ │ ┌─────────────────────Perch └─────────┤ │ ┌─────────────Alligator └───────┤ │ ┌──────Horse └──────┤ │ ┌───Chimp └──┤ │ └───Human|-------------|-------------|------------|------------|------------|------------|------------|------------|Sequence Difference
Sequence differences among vertebrate hemoglobins
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Neutral Theory of Molecular Evolution• Kimura (1968)
• Mutations can be:– Advantageous– Detrimental– Neutral (no good or bad phenotypic effect)
• Advantageous mutations are rapidly fixed, but really rare
• Diadvantageous mutations are rapidly eliminated
• Neutral mutations accumulate
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What Happens to a Neutral Mutation?
• Frequency subject to random chance
• Will carrier of gene reproduce?
• Many born but few survive– Partly selection– Mostly dumb luck
• Gene can have two fates– Elimination (frequent– Fixation (rare)
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Genetic Drift in Action
Ow!
Our green genes are evolutionarily superior!
Never mind…
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Simulation of Genetic Drift• 100 Mutations x 100 generations:
• 1 gets fixed• 2 still exist• 97 eliminated (most almost immediately)
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Rates of Change
CLOCK MOLECULAR a becan on accumulati change Therefore
CONSTANT. ison accumulati change Therefore
fixation. ofy probabilit theimesmutation t ofy probabilit on theonly depends R
out. cancels size population Therefore
1
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ratefixation
ratemutation
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Rate Overall
T
NR
NR
NRR
R
R
RRR
F
M
FM
F
M
FMT
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Protein Evolution RatesDifferent proteins have different rates
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Protein Evolution RatesDifferent proteins have different rates
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Rates (cont.)
• Slow rates in proteins critical to basic functions• E.g. histones ≈ 6 x 10-12 changes/a.a./year
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Rates (cont.)
Fibrinopeptides
• Theoretical max mutation rate• Last step in blood clotting pathway• Thrombin converts fibrinogen to fibrin
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Fibrinopeptides keep fibrinogens from sticking together.Fibrinopeptides keep fibrinogens from sticking together.
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Rates (cont.)
• Only constraint on sequence is that it has to physically be there
• Fibrinopeptide limit ≈ 9 x 10-9 changes/a.a./year
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Relationships among plant hemoglobinsArredondo-Peter, Raul, et al (1998) Plant Physiol. 118: 1121-1125
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Amino acid sequences of Amino acid sequences of several ribosome-inhibiting several ribosome-inhibiting proteinsproteins
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Phylogenetic trees built from the amino acid sequences of type 1 RIP or A chains (A) and B chains (B) of type 2 RIP (ricin-A, ricin-B, and lectin RCA-A and RCA-B from castor bean; abrin-A, abrina/b-B, and agglutinin APA-A and APA-B from A. precatorius; SNAI-A and SNAI-B, SNAV-A and SNAV-B, SNAI'-A and SNAI'-B, LRPSN1-A and LRPSN1-B, LRPSN2-A and LRPSN2-B, and SNA-IV from S. nigra; sieboldinb-A, sieboldinb-B, SSAI-A, and SSAI-B from S. sieboldiana; momordin and momorcharin from Momordica charantia; MIRJA from Mirabilis jalapa; PMRIPm-A and PMRIPm-B, PMRIPt-A and PMRIPt-B from Polygonatum multiflorum; RIPIriHol.A1, RIPIriHol.A2, and RIPIriHol.A3 from iris hybrid; IRAr-A and IRAr-B, IRAb-A and IRAb-B from iris hybrid; SAPOF from S. officinalis; luffin-A and luffin-B from Luffa cylindrica; and karasurin and trichosanthin from Trichosanthes kirilowii)
Hao Q. et.al. Plant Physiol. 2010:125:866-876Hao Q. et.al. Plant Physiol. 2010:125:866-876
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Phylogenetic tree of Opisthokonts, based on nuclear protein sequencesIñaki Ruiz-Trillo, Andrew J. Roger, Gertraud Burger, Michael W. Gray & B. Franz Lang (2008) Molecular Biology and Evolution, Jan 9