acetyl coa synthase: nature's monsanto acetic acid catalyst
TRANSCRIPT
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Presented by: Seth Cory and Trang Nguyen TAMU Fall 2014
Acetyl-coenzyme A Synthase: A Novel Organometallic Catalyst and Drug Target
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A Cluster: active site of ACS reaction
Proximal Ni: (trigonal planar) + where substrate binds + very labile can be removed by phenanthroline
Proximal Ni: (trigonal pyramid) can be replaced by Zn and Cu deactivates ACS
Ni
Lindahl, P. Coordination & Bioinorganic Chemistry Lectures, Nickel Enzyme, Texas A&M University, College Station. TX, USA, 2014
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Macharak, P; Harroop, T. Coord. Chem. Rev. 2005, 249, 3007-3024. Crabtree, R. The Organometallic Chemistry of the Transition Metals. 2005.
Active site of C-cluster Proposed Mechanism of C-cluster
How CO is delivered from C-cluster to A-cluster?
ACS/CODH Overview of Reaction
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BUT… the assembly chemistry of ACS is still unknown!!!
Darnault, C, et al. Nat. Struct. Biol. 2003, 10, 271-278.
Structure of ACS/CODH
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diffusion
Corrinoid Fe4S4 protein
????
Closed conformation Open conformation
What is the interface domain between CoFeSP and A cluster?
ACS/CODH Overview of Reaction
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Understand the chemical mechanism of A-cluster
Ni2+N
S N
S
O
Ni0S
2+/1+[Fe4S4]
Ni2+N
S N
S
O
Ni2+S2+/1+[Fe4S4]
Ni2+N
S N
S
O
Ni2+
S2+/1+[Fe4S4]
Ni2+N
S N
S
O
Ni2+
S2+/1+[Fe4S4]
CO
CH3Co3+-CoFeSP Co1+-CoFeSP
CO
H3C
Migratory InsertionH3C
O
CoAS-
H3C S
O
CoA
H3C
Dimagnetic Mechanism
Step 1: Oxidative elimination with CH3
- (Ni0 Ni2+) Step 2:
CO association (Ni2+)
Why do we study these interactions?
Adapted from: Lindahl, P. Met. Ions Life Sci. 2009, 6, 133-150.
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Understand the chemical mechanism of A-cluster
Ni2+N
S N
S
O
Ni1+S2+[Fe4S4]
Ni2+N
S N
S
O
Ni1+S2+[Fe4S4]
Ni2+N
S N
S
O
Ni2+
S2+[Fe4S4]
Ni2+N
S N
S
O
Ni3+S
2+[Fe4S4]
CO
CH3Co3+-CoFeSP
Co1+-CoFeSP
CO
CO
H3CMigratory Insertion
H3C
O
CoAS-
H3C
S
O
CoA
Ni2+ is activated by a 1e-
reduction by ferredoxin
Ni2+N
S N
S
O
Ni2+S
2+[Fe4S4]
CO
H3C
Internal e- transfer
Paramagnetic Mechanism
Step 1: CO association (Ni1+)
Step 2: Oxidative elimination
with CH3-
(Ni1+ Ni3+)
Why do we study these interactions?
Adapted from: Ragsdale, S; et. al. Chem. Rev. 2014, 114, 4149-4174.
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Why do we study these interactions?
Understand the chemical mechanism of A-cluster
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Monsato Acetic Acid Acetyl CoA Synthase
OXIDATIVE ADDITION with methyl group is a rate-limiting step
Temperature: 150-200 oC Temperature: 60-65 oC Pressure: 30-60 bar Pressure: 1 bar
How can we find the answer????
Lindahl, P. Coordination & Bioinorganic Chemistry Lectures, Nickel Enzyme, Texas A&M University, College Station. TX, USA, 2014
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Why do we study these interactions?
Understand the chemical mechanism of A-cluster
Develop novel catalysts in industrial reactions
TAMU CHEM 462
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Aim 3: To study the dynamics ACS/CODH enzyme
Aim 2: To probe coordination sphere of the A cluster
Aim 1: To study the methyl transfer from CoFeSP to ACS active site
Proposals for studying Acetyl CoA Synthase
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How can we study these interactions?
Ando, N.,et al. J. Am. Chem. Soc. 2012, 134, 17945–17954.
Darnault, C, et al. Nat. Struct. Biol. 2003, 10, 271-278.
Biophysical Techniques to study the interactions
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Ribonucleotide Reductases: A Model Study
Small Angle
X-ray Scattering
Experimental solution
scattering
Electron
Microscopy
X-ray
crystallography
Ando, N; et al. Proc. Natl. Acad. Sci. USA. 2011, 108, 21046-21051.
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Small Angle Xray Scattering
Molecular Envelopes
Electron Microscopy
Barondeau, D. Physcial Methods in Biological Chemistry, Structural Techniques, Texas A&M University, College Station. TX, USA, 2013
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X-ray Crystallography
Barondeau, D. Physcial Methods in Biological Chemistry, Structural Techniques, Texas A&M University, College Station. TX, USA, 2013
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How can we study these interactions?
Electron Microscopy (EM)
Small Angle X-ray Scattering (SAXS)
X-ray Crystallography (XTAL)
Ando, N.,et al. J. Am. Chem. Soc. 2012, 134, 17945–17954.
Darnault, C, et al. Nat. Struct. Biol. 2003, 10, 271-278.
Biophysical Techniques to study the interactions
Structural insight
at the interface
of CoFeSP & ACS
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How can we study these interactions?
Ando, N.,et al. J. Am. Chem. Soc. 2012, 134, 17945–17954.
Darnault, C, et al. Nat. Struct. Biol. 2003, 10, 271-278.
Docking Model between CoFeSP & ACS/CODH
Site-directed Mutagenesis at the interface
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Aim 3: To study the dynamics ACS/CODH enzyme
Aim 2: To probe coordination sphere of the A cluster
Aim 1: To study the methyl transfer from CoFeSP to ACS active site
Proposals for studying Acetyl CoA Synthase
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Site-directed Mutagenesis of A-cluster
Fontecilla-Camps, Handbook of Metalloproteins. 397-412
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Design primers with site-directed mutagenesis
Polymerase Chain Reaction (PCR)
DpnI Digestion & Transformation to E.coli cells
DNA sequencing to confirm the site-directed mutagenesis
Grow cells in large scale to obtain cell lysates
PURIFY the proteins (variants)
Site-directed Mutagenesis Procedure
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2. Kinetics with Crystallography
Site-directed Mutagenesis of A-cluster
1. Functional Assays: Acetyltransferase activity Acetyl CoA synthesis reaction rate
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𝛂 subunit 𝛂 subunit 𝛃 subunit
𝐀𝐀𝐀 𝐀𝐀𝐀 𝐀𝐂𝐂𝐂 Open conformation Tunnel is obstructed NO binding of CO
Closed conformation Tunnel is open Binding of CO
CO
What are the dynamics of the protein?
Structure of ACS/CODH
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Aim 3: To study the dynamics of ACS/CODH enzyme
Aim 2: To probe coordination sphere of the A cluster
Aim 1: To study the methyl transfer from CoFeSP to ACS active site
Proposals for studying Acetyl CoA Synthase
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Docking Model between ACS & CoFeSP
Predict the binding domain between CoFeSP & ACS/CODH
Strategy: Fluorescence Labeling at Specific Residues
a) Fluorescence Resonance Energy Transfer
A A
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Docking Model between CoFeSP & ACS/CODH
Predict the binding domain between CoFeSP & ACS/CODH
Strategy : Fluorescence Labeling at Specific Residues
a) Fluorescence Resonance Energy Transfer
b) Fluorescence Anisotropy
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Fluorescence Anisotropy
Experimental Techniques to study:
Open conformation Closed conformation
Docking Model between CoFeSP & ACS/CODH
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Understand the methyl transfer from CoFeSP to ACS
Understand the dynamics of ACS
Understand
the chemistry
of ACS
Conclusion
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Signs & Symptoms: Severe diarrhea Colitis Toxic megacolon Intestinal perforations
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How serious is CDI?
McCollum DL, Rodríguez M. Clin. Gastroenterol. Hepatol , 2012, 10, 581-592.
Current Treatments: Vancomycin: inhibitor of bacterial cell wall synthesis Metronidazole: inhibitor of bacterial DNA synthesis Antibiotics
Resistance A drive to find new target for the treatment of CDI
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Acetyl CoA Synthase: a new target for CDI treatment
Zhu, X. et al. Metallo., 2013, 5, 551-558.
3 potent inhibitors to inactivate ACS potent to C.difficile: 8-hydroxyquinoline 1,10-phenanthroline 2,2-dipyridyl
Inhibit methyl transfer
New antibiotics for CDI treatment
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Understanding the chemistry of ACS is important to the following fields: Bioinorganic Chemistry Biomimetic/Organometallic Catalysis Medicinal Chemistry
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Overview
McCollum DL, Rodríguez M. Clin. Gastroenterol. Hepatol , 2012, 10, 581-592.
Several biophysical and biochemical studies need to be done TEM, SAXS, X-ray crystallography Site-directed mutagenesis Fluorescent studies