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1.
Protein Sci ; 24(4): 484-94, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25377949

ABSTRACT

Conformational changes in the ß2α2 and ß6α6 loops in the alpha subunit of tryptophan synthase (αTS) are important for enzyme catalysis and coordinating substrate channeling with the beta subunit (ßTS). It was previously shown that disrupting the hydrogen bond interactions between these loops through the T183V substitution on the ß6α6 loop decreases catalytic efficiency and impairs substrate channeling. Results presented here also indicate that the T183V substitution decreases catalytic efficiency in Escherchia coli αTS in the absence of the ßTS subunit. Nuclear magnetic resonance (NMR) experiments indicate that the T183V substitution leads to local changes in the structural dynamics of the ß2α2 and ß6α6 loops. We have also used NMR chemical shift covariance analyses (CHESCA) to map amino acid networks in the presence and absence of the T183V substitution. Under conditions of active catalytic turnover, the T183V substitution disrupts long-range networks connecting the catalytic residue Glu49 to the αTS-ßTS binding interface, which might be important in the coordination of catalytic activities in the tryptophan synthase complex. The approach that we have developed here will likely find general utility in understanding long-range impacts on protein structure and dynamics of amino acid substitutions generated through protein engineering and directed evolution approaches, and provide insight into disease and drug-resistance mutations.


Subject(s)
Catalytic Domain , Hydrogen Bonding , Tryptophan Synthase/chemistry , Tryptophan Synthase/metabolism , Amino Acids/chemistry , Amino Acids/metabolism , Escherichia coli Proteins/chemistry , Escherichia coli Proteins/metabolism , Kinetics , Models, Molecular , Nuclear Magnetic Resonance, Biomolecular , Protein Conformation , Protein Subunits/chemistry , Protein Subunits/metabolism
2.
J Am Chem Soc ; 136(19): 6818-21, 2014 May 14.
Article in English | MEDLINE | ID: mdl-24766576

ABSTRACT

Proteins can be viewed as small-world networks of amino acid residues connected through noncovalent interactions. Nuclear magnetic resonance chemical shift covariance analyses were used to identify long-range amino acid networks in the α subunit of tryptophan synthase both for the resting state (in the absence of substrate and product) and for the working state (during catalytic turnover). The amino acid networks observed stretch from the surface of the protein into the active site and are different between the resting and working states. Modification of surface residues on the network alters the structural dynamics of active-site residues over 25 Å away and leads to changes in catalytic rates. These findings demonstrate that amino acid networks, similar to those studied here, are likely important for coordinating structural changes necessary for enzyme function and regulation.


Subject(s)
Amino Acids/chemistry , Salmonella typhimurium/enzymology , Tryptophan Synthase/chemistry , Amino Acids/metabolism , Catalytic Domain , Kinetics , Models, Molecular , Nuclear Magnetic Resonance, Biomolecular , Protein Conformation , Protein Subunits/chemistry , Protein Subunits/metabolism , Salmonella typhimurium/chemistry , Tryptophan Synthase/metabolism
3.
Protein Sci ; 23(3): 302-11, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24403092

ABSTRACT

Substrate binding, product release, and likely chemical catalysis in the tryptophan biosynthetic enzyme indole-3-glycerol phosphate synthase (IGPS) are dependent on the structural dynamics of the ß1α1 active-site loop. Statistical coupling analysis and molecular dynamic simulations had previously indicated that covarying residues in the ß1α1 and ß2α2 loops, corresponding to Arg54 and Asn90, respectively, in the Sulfolobus sulfataricus enzyme (ssIGPS), are likely important for coordinating functional motions of these loops. To test this hypothesis, we characterized site mutants at these positions for changes in catalytic function, protein stability and structural dynamics for the thermophilic ssIGPS enzyme. Although there were only modest changes in the overall steady-state kinetic parameters, solvent viscosity and solvent deuterium kinetic isotope effects indicated that these amino acid substitutions change the identity of the rate-determining step across multiple temperatures. Surprisingly, the N90A substitution had a dramatic effect on the general acid/base catalysis of the dehydration step, as indicated by the loss of the descending limb in the pH rate profile, which we had previously assigned to Lys53 on the ß1α1 loop. These changes in enzyme function are accompanied with a quenching of ps-ns and µs-ms timescale motions in the ß1α1 loop as measured by nuclear magnetic resonance studies. Altogether, our studies provide structural, dynamic and functional rationales for the coevolution of residues on the ß1α1 and ß2α2 loops, and highlight the multiple roles that the ß1α1 loop plays in IGPS catalysis. Thus, substitution of covarying residues in the active-site ß1α1 and ß2α2 loops of indole-3-glycerol phosphate synthase results in functional, structural, and dynamic changes, highlighting the multiple roles that the ß1α1 loop plays in enzyme catalysis and the importance of regulating the structural dynamics of this loop through noncovalent interactions with nearby structural elements.


Subject(s)
Catalytic Domain , Indole-3-Glycerol-Phosphate Synthase/chemistry , Sulfolobus solfataricus/enzymology , Amino Acid Substitution , Catalysis , Circular Dichroism , Enzyme Stability , Genes, Archaeal/physiology , Indole-3-Glycerol-Phosphate Synthase/metabolism , Kinetics , Models, Molecular , Protein Structure, Secondary , Protein Structure, Tertiary , Sulfolobus solfataricus/chemistry
4.
J Biol Chem ; 288(37): 26350-6, 2013 Sep 13.
Article in English | MEDLINE | ID: mdl-23900843

ABSTRACT

The tryptophan biosynthetic enzyme indole-3-glycerol phosphate synthase is a proposed target for new antimicrobials and is a favored starting framework in enzyme engineering studies. Forty years ago, Parry proposed that the enzyme mechanism proceeds through two intermediates in a series of condensation, decarboxylation, and dehydration steps. X-ray crystal structures have suggested that Lys-110 (numbering according to the Sulfolobus solfataricus enzyme) behaves as a general acid both in the condensation and dehydration steps, but did not reveal an efficient pathway for the reprotonation of this critical residue. Our mutagenesis and kinetic experiments suggest an alternative mechanism whereby Lys-110 acts as a general acid in the condensation step, but another invariant residue, Lys-53, acts as the general acid in the dehydration step. These studies also indicate that the conserved residue Glu-51 acts as the general base in the dehydration step. The revised mechanism effectively divides the active site into discrete regions where the catalytic surfaces containing Lys-110 and Lys-53/Glu-51 catalyze the ring closure (i.e. condensation and decarboxylation) and dehydration steps, respectively. These results can be leveraged toward the development of novel inhibitors against this validated antimicrobial target and toward the rational engineering of the enzyme to produce indole derivatives that are highly prized by the pharmaceutical and agricultural industries.


Subject(s)
Catalytic Domain , Indole-3-Glycerol-Phosphate Synthase/chemistry , Anti-Bacterial Agents/chemistry , Catalysis , Crystallography, X-Ray , Escherichia coli/enzymology , Glutamic Acid/chemistry , Lysine/chemistry , Mutagenesis, Site-Directed , Protein Engineering , Solvents , Tryptophan/chemistry , Viscosity
5.
Appl Biochem Biotechnol ; 170(5): 1138-50, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23645415

ABSTRACT

The potential utility of an imaging agent for the detection of hepatic copper was investigated in a Wilson's disease animal model. Solid-phase peptide synthesis was used to construct an imaging agent which consisted of a copper-binding moiety, taken from the prion protein, and a gamma ray-emitting indium radiolabel. Long-Evans Cinnamon (LEC) rats were used for the Wilson's disease animal model. Our evaluation methodology consisted of administering the indium-labeled agent to both LEC and genetically healthy Long-Evans (LE) cohorts via a tail vein injection and following the pharmacokinetics with single-photon emission computed tomography (SPECT) over the course of an hour. The animals were then sacrificed and their livers necropsied. An additional control agent, lacking the copper-binding moiety, was used to gauge whether any change in the hepatic uptake might be caused by other physiological differences between the two animal models. LEC rats injected with the indium-labeled agent had roughly double the amount of hepatic radioactivity as compared to the healthy control animals. The control agent, without the copper-binding moiety, displayed a hepatic signal similar to that of the control LE animals. Additional intraperitoneal spiking with CuSO4 in C57BL/6 mice also found that the pharmacokinetics of the indium-labeled, prion-based imaging agent is profoundly altered by exposure to in vivo pools of extracellular copper. The described SPECT application with this compound represented a significant improvement over a previous MRI application using the same base peptide sequence.


Subject(s)
Copper/metabolism , Hepatolenticular Degeneration/metabolism , Indium Radioisotopes/pharmacokinetics , Liver/metabolism , Tomography, Emission-Computed, Single-Photon/methods , Animals , Hepatolenticular Degeneration/diagnostic imaging , Liver/diagnostic imaging , Male , Metabolic Clearance Rate , Mice , Mice, Inbred C57BL , Molecular Imaging/methods , Radiopharmaceuticals/pharmacokinetics , Rats , Rats, Inbred LEC , Tissue Distribution
6.
Appl Biochem Biotechnol ; 168(3): 504-18, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22810201

ABSTRACT

Abnormal distributions of transition metals inside the body are potential diagnostic markers for several diseases, including Alzheimer's disease, Parkinson's disease, Wilson's disease, and cancer. In this article, we demonstrate that P57/Gd, a novel prion-based contrast agent, can selectively image tissues with excessive copper accumulation using magnetic resonance imaging (MRI). P57/Gd selectivity binds copper(II) over other physiologically relevant cations such as zinc, iron, manganese, and calcium. To simulate a metabolic copper disorder, we treated mice with an intraperitoneal injection of a CuSO(4) solution to induce a renal copper overload. The MRI signal intensities from the renal cortex and medulla of copper spiked animals that were administered P57/Gd were found to correlate with the ex vivo copper concentrations determined by inductively coupled plasma mass spectrometry.


Subject(s)
Copper/analysis , Magnetic Resonance Imaging/methods , Whole Body Imaging/methods , Animals , Contrast Media/chemistry , Contrast Media/metabolism , Magnetic Resonance Imaging/instrumentation , Male , Mice , Mice, Inbred C57BL , Mice, Inbred ICR , Prions/chemistry , Prions/metabolism , Rats , Rats, Sprague-Dawley , Whole Body Imaging/instrumentation
7.
Biometals ; 25(2): 337-50, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22080191

ABSTRACT

Abnormal distributions of transition metals inside the brain are potential diagnostic markers for several central nervous system diseases, including Alzheimer's disease (AD), Parkinson's disease, dementia with Lewy bodies (DLB), bipolar disorders and depression. To further explore this possibility, the total concentrations of iron, zinc, copper, manganese, aluminum, chromium and cadmium were measured in post-mortem hippocampus and amygdala tissues taken from AD, DLB and Control patients. A statistically significant near fifty percent reduction in the total copper levels of AD patients was observed in both the hippocampus and amygdala. The statistical power of the hippocampus and amygdala copper analysis was found to be 86 and 74% respectively. No statistically significant deviations in the total metal concentrations were found for zinc, manganese, chromium or aluminum. Iron was found to be increased by 38% in AD amygdala tissues, but was unchanged in AD hippocampus tissues. Accounting for differences in tissue water content, as a function of both tissue type and disease state, revealed more consistencies with previous literature. To aid in the design of future experiments, the effect sizes for all tissue types and metals studied are also presented.


Subject(s)
Amygdala/chemistry , Dementia/metabolism , Hippocampus/chemistry , Transition Elements/analysis , Aged , Aged, 80 and over , Alzheimer Disease/metabolism , Copper/analysis , Female , Humans , Iron/analysis , Lewy Body Disease/metabolism , Male , Parkinson Disease/metabolism , Zinc/analysis
8.
J Chem Theory Comput ; 6(2): 438-42, 2010 Feb 09.
Article in English | MEDLINE | ID: mdl-26617300

ABSTRACT

The ability of an empirical, polarizable model of water to predict a thermal ensemble of molecular configurations at ambient conditions was examined using first-principle quantum mechanics. The empirical model of water selected for this evaluation was the TTM2-F model. The quantum mechanical methodology selected was the second-order Møller-Plesset model (MP2). Only pairwise interaction energies were considered. Significant deviations from the empirical model were found. Similar results were found for ad-hoc comparisons with several other common water models including the TIP3P, TIP4P, TIP4P-FQ, TIP5P, TTM2.1-F, TTM2.2-F, TTM3-F, and POL5/QZ potential models. Our results show that spatially close dimer configurations with interaction energies notably above the potential well minimum (but are still thermally accessible at ambient conditions) are the source of the largest deviations. To assist others in future water model parametrizations we report the MP2 near complete basis set limit energies for 840 water dimer configurations sampled from an approximate thermal ensemble at ambient conditions.

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