biochemical examples of chem321/322 concepts
DESCRIPTION
Biochemical Examples of CHEM321/322 Concepts. Stereochemistry. Many biomolecules, including proteins, carbohydrates and DNA, are chiral. - PowerPoint PPT PresentationTRANSCRIPT
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Biochemical Examples of CHEM321/322 Concepts
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Stereochemistry
• Many biomolecules, including proteins, carbohydrates and DNA, are chiral.
• A typical drug molecule acts by docking with a target biomolecule such as an enzyme or receptor. These drugs are often chiral, and the two enantiomers may differ greatly in efficacy.
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Resolution of Naproxen
• Naproxen is an NSAID (Non-Steroidal Anti-Inflammatory Drug).
• The (+)-(S)-enantiomer of naproxen is the active isomer. It is synthesized as a racemate then resolved with an enantiopure amine base and sold as a single enantiomer.
3
MeO
OH
O
(+)-(S)-naproxen
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• NSAIDS act by inhibiting cyclooxygenase enzymes (COX). These enzymes convert arachidonic acid to prostaglandins, some of which are involved in inflammation.
4
CO2H
COXOO
OOH
CO2H prostaglandins
prostacyclins
thromboxanes
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Epimerization
• Epimers are stereoisomers that differ at only one stereocenter. Epimerization refers to a chemical process that interconverts epimers.
• A stereocenter a- to a carbonyl can epimerize via the enol or enolate. e.g.:
6
COHHHHOOHHOHH
CH2OH
CC OH
HHOOHHOHH
CH2OH
CHHOHHOOHHOHH
CH2OH
H O OHH O
Ca(OH)2
glucose mannose
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Epimerization of Paclitaxel (Taxol™)
• Paclitaxel, an inhibitor of mitosis, is used in chemotherapy
• Epimerization via retro-Aldol:
7
OO
NH
OH O O
O
HO
O OH
OO
O
OO
base
H OO
NH
OH O O
O
HO
O OH
OO
O
OO
H
OAcO
OO
H OAcO
O
H OAcO
OHO
H
H OH H
O
H OH
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Thalidomide
• Was prescribed in 1957-62 for conditions that included insomnia and morning sickness in pregnant women.
• The (R)- isomer gives the desired sedative effect.• The (S)- isomer is a teratogen.
• Epimerization in the body is rapid, so an enantiopure drug would not prevent birth defects
8
NNH
O
O
O
O
*
thalidomide
Carl Zimmer, New York Times 3/15/2010.
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Thousands of babies worldwide, whose mothers had been prescribed thalidomide during pregnency, were born with severe deformities, particularly stunted and deformed limbs.
The insistence of pharmacologist Frances Oldham Kelsey for more safety data delayed approval of thalidomide in the U.S. In 1962, the teratogenic effects of thalidomide became widely know, and the drug maker withdrew its U.S. drug application.
9http://pubs.acs.org/cen/coverstory/83/8325/8325thalidomide.htmlhttp://www.flickr.com/photos/vivacomopuder/2531635433/
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Amines and acids prefer acid-base chemistry
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Formation of Peptide Bonds
• Simply mixing carboxylic acids and amines together is generally not an effective way to make peptide bonds.
• The ions that result from the acid/base reaction between the two components predominate and are inert to acylation-type reactions.
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A Coupling Reagent; Couples Amines and Acids
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Direct Treatment of Amino Acids with DCC leads to
uncontrolled polymerization
“Real peptides” are of specific sequence.
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Need protecting group
Now:
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Purification of each reaction is a Pain!; Merifield’s Solid-
supported synthesis
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Merrifield automated peptide synthesizerca. 1964
Chemical Heritage Museum, Philadelphia17
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How does nature make peptides/proteins?
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-A-U-G - C-C-U - U-A-C - C-C-G - A-U-C-C-C-U-
-A-U-G - C-C-U - U-A-C - C-C-G - A-U-C - C-C-U-
mRNA
How does nature make peptides/proteins?
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http://www.rcsb.org/pdb/
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How does nature make How do you make acyl-tRNAs?
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The Ribosome 3 RNA fragments + 31Proteins; IT’S BIG
Structure of the 5’ half of the large ribosomal subunit. Grey = RNAGold = protein
2.6 million daltons!
Structure by T. Steitz and P. Moore (Yale)
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Three tRNAs in modeled in the core of the ribosome
The peptide tunnelExit ->
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How do you break amide
bonds?
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Mechanism of Amide bond hydrolysisAcid:
Base:
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Beta Lactam Antibiotics & Resistance
Cool movie at: http://www.cellsalive.com/qtmovs/penpop_mov.htm
Bacteria are protected from osmotic stress by a strong heavily crosslinked peptidoglycan (protein+carbohydrate coating)
Bacteria need to be able to synthesize a strong cell wall in order to reproduce and survive.
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Crosslinking is needed for strength
transpeptidease
like spaghetti like netting
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If you block the transpeptidease bacteria cant replicate and will burst.
Cool movie at: http://www.cellsalive.com/qtmovs/penpop_mov.htm
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How beta-lactams work
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The strained beta-lactam acts an an acylating agent of active site serine.
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The bacterium fight back!
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Betalactamase destroys betalactams
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Build a better beta-lactam?
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Another approach: cap the isopeptide chain
The natural product drug vancomycin caps the isopeptide
vancomycin
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Vancomycin
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Some bacterium have learned to modify their isopeptide to contain an ester linkage.
Vancomycin no longer binds the lactate containing isopeptide strong enough to block the transpeptidase.
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HIVHow to stop a killer
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HIV
R.T.
HIV protease
RNA DNA
Functional Proteins
Designing Better anti-AIDS Drugs
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Another view at HIV protease
Top View Cross section with peptide Cross section
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From: www.dsch.units.it/~benedetti
Note Tetrahedral Intermediate
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Protease Inhibitor
Mimics Tetrahedral Intermediate
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Several HIV proteases have been
been developed
Annual Review of Pharmacology and ToxicologyVol. 40: 649-674
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HIV resistance
Many strains are now known that have mutated their HIV protease specificity in response to protease inhibitors.By identifying the common feature of these proteases, chemists are tying to develop new “universal” inhibitors.
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Reversible vs. Irreversible Inhibition
• The HIV protease inhibitors discussed earlier are reversible inhibitors. They mimic the shape of the substrate reaction’s transition state, but bind to the enzyme by weak intermolecular forces.
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Reversible vs. Irreversible Inhibition
• An inhibitor can also chemically react with its target and bind irreversibly via covalent bond formation. (“suicide inhibition”)
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Acetylcholinesterase (AChE)
• Acetylcholine is a neurotransmitter found at neuromuscular junctions.
• After its release into the synapse, rapid hydrolysis of acetylcholine is critical for continued nerve function
ON
O
acetylcholine
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• A neutral hydroxyl (e.g. Ser-OH) isn’t a very good nucleophile, but deprotonation would require a strong base
• “Catalytic triad”: a glutamate (or aspartate) carboxylate hydrogen-bonds with a histidine’s imidazole group, which increases its basicity enough to assist with removal of serine’s hydroxyl proton.
• The oxygen can then attack the substrate nucleophilically when the substrate binds to the active site.
56
Glu
O OH
N NH O
Ser
His
Glu
O OH
N N H OSer
Hissubstrate
binding
Substrate Substrate
"Catalytic Triad"
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O
O
NN
OH
H
HN
N
OO
NH O
NH O
G117
G116
S198
H438G325
W82
Transesterification of acetylcholine in AChE active site
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Organophosphorous Neurotoxins
• Sarin and similar neurotoxins irreversibly inhibit AChE by reacting with Ser-OH
OP O
F
OP O
F
OP O
S
OP ON
C
SarinGB
SomanGD
NN(iPr)2VX Tabun
GA
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O
O
NN
OH
HH
HN NH O
NH O
G117
G116
S198
H438G325
W82
POOROR/NR2
OP O
F
OP O
F
OP O
S
OP ON
C
SarinGB
SomanGD
NN(iPr)2
VX TabunGA
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Oxidation/Reduction
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Cannizzaro Reaction
• An aldehyde acts as both oxidizing and reducing agent in a disproportionation reaction.
• Mechanism features hydride (H:-) as a leaving group ?!?!?!?!?!?!?!?!
O
H2O
OHOH+NaOH
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Ph
O
H
hydrate formation
+ deprotonation Ph
O O
H Ph
O
H
Ph
O
O Ph H
H O
Cannizzaro Mechanism
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NAD+/NADH
N
NN
N
NH2
O
OHOH
OP-O
O
O
N
O
OHOH
OP-OO
O
O
O
NH2
N
NN
N
NH2
O
OHOH
OP-O
O
O
N
O
OHOH
OP-OO
O
O
O
NH2
H+
- H
HH
NAD+ NADH
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N
NN
N
NH2
O
OPO32-OH
OP-O
O
O
N
O
OHOH
OP-OO
O
O
O
NH2
N
NN
N
NH2
O
OPO32-OH
OP-O
O
O
N
O
OHOH
OP-OO
O
O
O
NH2
H+
- H
HH
NADP+ NADPH
NADP+/NADPH
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• Anabolism: biosynthetic processes (“building”), e.g. synthesizing glucose from CO2 and H2O.
• Catabolism: degradative processes (“destroying”), e.g. oxidizing glucose to CO2 and H2O.
• Combined: Metabolism
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• NAD+ is generally used as an oxidizing agent in catabolism (e.g. citric acid cycle). The NADH produced is primarily used to produce ATP.
• NADPH is primarily used as a reducing agent (hydride donor) in anabolic processes.
• The phosphate “tag” on NADPH allows for independent regulation of levels of NAD+/NADH and NADP+/NADPH
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Reduction of Carbonyls with NADPH
• “Nature’s version of LAH”
N
O
NH2
HH
N
O
NH2
OH
NADPH NADP+
HO H
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O SCoA
O OOH
2 NADPH2 NADP+ + CoASH
O OH
O OH
HMG CoAreductase mevalonateHMG CoA
HMG CoA Reductase is the Target of Statin Drugs
• HMG CoA reductase catalyzes the rate-limiting step of cholesterol biosynthesis
• Lipitor™ (atorvastatin) became the best-selling pharmaceutical in history in 2003.
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Reduction of HMG CoA with NADPH
• Reduction of a thioester (sulfur analogue of ester) with NADPH — similar to reduction of an ester with LAH
• What is “SCoA”? Let’s look at the important thioester Acetyl CoA:
O SCoA
O OOH
2 NADPH2 NADP+ + CoASH
O OH
O OH
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Acetyl CoA
• CoA thioesters are common acyl transfer units.
• Acetyl CoA is a common 2-carbon building block.
O
SCoA=
O
SHN
HN
OHP
OHP
OO O
OH
N
NN
N
NH2
O
OHOH
CoA = "Coenzyme A"
acetyl CoA
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Nature Uses Claisen-Like Condensations
• First step in HMG CoA synthesis:
• Very similar to CHEM 322!
EnzymeS
O
O
SCoAH
B
EnzymeS
O
SCoA
O
B H
O O
SCoA
acetoacetyl CoAacetyl CoA
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Nature Uses Aldol-Like Condensations
OO
EnzS
enzyme-boundacetoacetyl
O
SCoAH acetyl CoA
B:
H
O
EnzS
HO O
SCoA
hydrolysis
O SCoA
O OOH
HMG CoA
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How Do You Get From
HO
cholesterol
H
H
H
O OH
O OH
mevalonateto
?
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• Mevalonate is converted to isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP):
O OH
O OH
mevalonate
ATP ADP
O OPP
O OPO32-
O OPP
O
OPP
IPPOPP
DMAPP
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IPP/DMAPP Are Nature’s Equivalent of Isoprene
• Natural rubber (latex): polyisoprene
OPP
IPP
OPP
DMAPP isoprene
ndouble bonds all Z- !
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Synthesis of CholesterolIPP/DMAPP
OPP
farnesyl diphosphate
squalene
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squalene
HOO
H
squalene oxide lanosterol
H
!
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HO
lanosterolH
HO
cholesterol
H
H
H
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Glycolysis
OHO
HO
OHOHH
OH
2O
O
O
glucoseC6
pyruvate2 x C3
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CHOOHHHHOOHHOHH
CH2OH
CHOOHHHHOOHHOHH
CH2OPO32-
CH2OHOHHOOHHOHH
CH2OPO32-
CH2OPO32-
OHHOOHHOHH
CH2OPO32-
ATP ADP phospho-glucose
isomerase
ATP ADP
glucose glucose 6-phosphate
fructose 6-phosphate fructose 1,6-biphosphate
costs
2 ATP
Activation of Glucose
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Retro-Aldol to Glyceraldehyde 3-Phosphate
CH2OPO32-
OHHOOHOHH
CH2OPO32-
fructose1,6-biphosphate
"retro-aldol"
H
H CH2OPO32-
C OHC HHO
C OHC OHHCH2OPO3
2-
taut CH2OPO32-
C OCH2OH
glyceraldehyde3-phosphate
(G3P)
dihydroxyacetonephosphate
(DHAP)
+
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Not Exactly “Retro-Aldol”• In plants and animals, fructose 1,6-biphosphate
reacts at active site to form an imine (Schiff base):
• (+) charge on N makes this “retro-aldol” mechanism more facile
Lys-NH2
CH2OPO32-
OHHOOHOHH
CH2OPO32-
fructose1,6-biphosphate
H
CH2OPO32-
HHOOHOHH
CH2OPO32-
H
NLys
protonated imine("Schiff base")
H
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DHAP/G3P Rapidly Interconvert Enzymatically
C OHC OHHCH2OPO3
2-
CH2OPO32-
CCH
HO
O
H
NN H
B H
His
O2C Glu
CH2OPO32-
C
CO
HO
H
NN
B
His
C Glu
H
HO
OH
CC HHOCH2OPO3
2-
O H
DHAP
G3P
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• Triose phosphate isomerase catalyzes the interconversion of DHAP and G3P
• Example of a “kinetically perfect” enzyme – rate-limiting step is diffusion
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Fates of G3P/Pyruvate
C OHC OHHCH2OPO3
2-
G3P
CO2
O
pyruvate
anaerobicCO2
OHEtOH
lactate (fermentation)
or
2 ATP per glucose
aerobic
acetyl CoA
+ CO2SCoA
O
ca. 30 ATP per glucose!!!(after citric acid cycle/
oxidative phosphorylation)Cool chemistry omitted!
(e.g. Vitamin B1)
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Citric Acid Cycle
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Citric Acid Cycle
Aldol-type condensation(using enol of acetyl CoA)
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Citric Acid Cycledehydration ofaldol product
hydration(Michael addition)
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Citric Acid Cycle
oxidation to unstableb-keto acid
decarboxylation
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Citric Acid Cycle
similar mechanism to pyruvate - acetyl CoA
(vitamin B1)
similar interconversions of carboxylic acid derivatives
as in Ch.
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Citric Acid Cycle
dehydrogenation(reverse of hydrogenation)
hydration(Michael)
alcohol oxidation
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Fatty Acid Metabolism
See Section 19.10 of text!