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1.
Clin Radiol ; 74(11): 897.e9-897.e16, 2019 Nov.
Article in English | MEDLINE | ID: mdl-31474302

ABSTRACT

AIM: To present a new protocol to optimise ultrasound (US) assessment of haemophilic arthropathy. MATERIALS AND METHODS: Ultrasound of haemophilic arthropathy joints was performed using three different ultrasound protocols, namely, the Toronto-Vellore Comprehensive Ultrasound (TVC-US) protocol, the Haemophilia Early Arthropathy Detection with Ultrasound (HEAD-US), and the newly developed Universal Simplified Ultrasound (US-US) protocol. Synovial hypertrophy, haemosiderin deposition, effusion, erosion, and cartilage loss were evaluated in 20 joints. The reliability and diagnostic efficiency of these protocols was compared using magnetic resonance imaging (MRI). RESULTS: The correlation between the TVC-US and US-US protocols for synovial hypertrophy was excellent: kappa significance (KS) was 1, but was substantial (KS=0.65) with the HEAD-US protocol. For effusion, both the TVC-US and the HEAD-US protocols had substantial correlation with the US-US protocol (KS=0.7 and 0.6 respectively). The correlation for erosion and cartilage loss was excellent between the TVC-US and the US-US with MRI (KS=1), but poor (KS=0) with the HEAD-US protocol. The US-US protocol also had good interobserver agreement (KS=1). CONCLUSION: The accuracy of the US-US protocol is comparable to the TVC-US protocol and MRI and is superior to the HEAD-US protocol in the assessment of haemophilic arthropathy.


Subject(s)
Ankle Joint/diagnostic imaging , Hemophilia A/complications , Knee Joint/diagnostic imaging , Temporomandibular Joint Disc/diagnostic imaging , Adolescent , Cartilage Diseases/diagnostic imaging , Cartilage Diseases/pathology , Child , Clinical Protocols , Connective Tissue/diagnostic imaging , Hemosiderin/analysis , Humans , Hypertrophy/diagnostic imaging , Magnetic Resonance Imaging , Osteochondrosis/diagnostic imaging , Osteochondrosis/pathology , Prospective Studies , Synovial Membrane/diagnostic imaging , Synovial Membrane/pathology , Temporomandibular Joint Disc/pathology , Time Factors , Ultrasonography , Young Adult
2.
Indian J Exp Biol ; 48(4): 407-14, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20726340

ABSTRACT

The crude buffer (Tris Buffer Saline-I) extracts of muscles, liver, kidney and heart of goat and chicken (White leghorn) were screened against 16 clinical isolates. Among the five tissues, the heart tissue of each animal showed significant bactericidal activities on many isolates. The acid extracted crude proteins of both heart tissues also showed significant antibacterial activities against many bacterial isolates. The crude proteins of goat heart tissues displayed strong bactericidal activities against Salmonella paratyphi 'A' and Salmonella typhimurium (MIC: 16 microg/ml) whereas thecrude proteins of chicken heart tissues displayed strong bactericidal activities against Escherichia coli ATCC and Pseudomonas aeruginosa at 16 and 63 microg/ml concentrations respectively. The peptides of low molecular weight ( <30 kDa) were also separated from the acid extracted crude proteins of goat and chicken heart tissues by SDS-PAGE after staining with silver nitrate solution.


Subject(s)
Anti-Bacterial Agents/pharmacology , Chickens , Goats , Heart , Peptides/pharmacology , Tissue Extracts/pharmacology , Animals , Anti-Bacterial Agents/isolation & purification , Electrophoresis, Polyacrylamide Gel , Enzyme-Linked Immunosorbent Assay , Escherichia coli/drug effects , Humans , Microbial Sensitivity Tests , Organ Specificity , Peptides/isolation & purification , Pseudomonas aeruginosa/drug effects , Salmonella/drug effects , Tissue Extracts/isolation & purification
3.
Biochemistry ; 42(19): 5600-8, 2003 May 20.
Article in English | MEDLINE | ID: mdl-12741816

ABSTRACT

Cytochrome c peroxidase (CCP) is a 32.5 kDa mitochondrial intermembrane space heme peroxidase from Saccharomyces cerevisiae that reduces H(2)O(2) to 2H(2)O by oxidizing two molecules of cytochrome c (cyt c). Here we compare the 1.2 A native structure (CCP) with the 1.3 A structure of its stable oxidized reaction intermediate, Compound I (CCP1). In addition, crystals were analyzed by UV-vis absorption and electron paramagnetic resonance spectroscopies before and after data collection to determine the state of the Fe(IV) center and the cationic Trp191 radical formed in Compound I. The results show that X-ray exposure does not lead to reduction of Fe(IV) and only partial reduction of the Trp radical. A comparison of the two structures reveals subtle but important conformational changes that aid in the stabilization of the Trp191 cationic radical in Compound I. The higher-resolution data also enable a more accurate determination of changes in heme parameters. Most importantly, when one goes from resting state Fe(III) to Compound I, the His-Fe bond distance increases, the iron moves into the porphyrin plane leading to shorter pyrrole N-Fe bonds, and the Fe(IV)-O bond distance is 1.87 A, suggesting a single Fe(IV)-O bond and not the generally accepted double bond.


Subject(s)
Cytochrome-c Peroxidase/chemistry , Crystallography, X-Ray , Electron Spin Resonance Spectroscopy , Enzyme Stability , Heme/chemistry , Hydrogen Bonding , Iron/chemistry , Models, Molecular , Molecular Structure , Oxidation-Reduction , Protein Conformation , Recombinant Proteins/chemistry , Saccharomyces cerevisiae/enzymology , Spectrophotometry , Spectrophotometry, Ultraviolet , Static Electricity
4.
Mol Microbiol ; 48(2): 295-303, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12675792

ABSTRACT

The ATPase activity of MinD is required for it to oscillate between the ends of the cell and spatially regulate cell division in Escherichia coli. It is a member of a functionally diverse subgroup of ATPases which are involved in activities ranging from nitrogen fixation (NifH) to plasmid segregation (ParA). All members of the subgroup have a deviant Walker A motif which contains a conserved 'signature' lysine that characterizes this subgroup. In the NifH homodimer the signature lysines make intermonomer contact with the bound nucleotides indicating a role in ATP hydrolysis. ATP binding to NifH leads to formation of an active dimer that associates with a partner that is also a dimer. Because ATP hydrolysis is coupled to formation of the complex, the complex is only transient. In the presence of ATP MinD binds MinC and goes to the membrane, however, the ATPase is not stimulated and the complex is stable. Subsequent interaction of this complex with MinE, however, leads to ATPase stimulation and release of the Min proteins from the membrane. The sequential interaction of MinD with these two proteins, which is dictated by the membrane, is critical to the oscillatory mechanism involved in spatial regulation of division.


Subject(s)
Adenosine Triphosphatases/chemistry , Adenosine Triphosphatases/metabolism , Amino Acid Motifs , Cell Membrane/metabolism , Escherichia coli Proteins/chemistry , Escherichia coli Proteins/metabolism , Adenosine Triphosphatases/genetics , Arsenite Transporting ATPases , Bacterial Proteins/chemistry , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Dimerization , Escherichia coli Proteins/genetics , Ion Pumps/chemistry , Ion Pumps/metabolism , Membrane Proteins/chemistry , Membrane Proteins/genetics , Membrane Proteins/metabolism , Models, Molecular , Multienzyme Complexes/chemistry , Multienzyme Complexes/metabolism , Oxidoreductases/chemistry , Oxidoreductases/metabolism , Protein Binding , Protein Structure, Tertiary
5.
Biochemistry ; 40(45): 13483-90, 2001 Nov 13.
Article in English | MEDLINE | ID: mdl-11695895

ABSTRACT

The crystal structure of the fully oxidized di-heme peroxidase from Nitrosomonas europaea has been solved to a resolution of 1.80 A and compared to the closely related enzyme from Pseudomonas aeruginosa. Both enzymes catalyze the peroxide-dependent oxidation of a protein electron donor such as cytochrome c. Electrons enter the enzyme through the high-potential heme followed by electron transfer to the low-potential heme, the site of peroxide activation. Both enzymes form homodimers, each of which folds into two distinct heme domains. Each heme is held in place by thioether bonds between the heme vinyl groups and Cys residues. The high-potential heme in both enzymes has Met and His as axial heme ligands. In the Pseudomonas enzyme, the low-potential heme has two His residues as axial heme ligands [Fulop et al. (1995) Structure 3, 1225-1233]. Since the site of reaction with peroxide is the low-potential heme, then one His ligand must first dissociate. In sharp contrast, the low-potential heme in the Nitrosomonas enzyme already is in the "activated" state with only one His ligand and an open distal axial ligation position available for reaction with peroxide. A comparison between the two enzymes illustrates the range of conformational changes required to activate the Pseudomonas enzyme. This change involves a large motion of a loop containing the dissociable His ligand from the heme pocket to the molecular surface where it forms part of the dimer interface. Since the Nitrosomonas enzyme is in the active state, the structure provides some insights on residues involved in peroxide activation. Most importantly, a Glu residue situated near the peroxide binding site could possibly serve as an acid-base catalytic group required for cleavage of the peroxide O--O bond.


Subject(s)
Cytochrome-c Peroxidase/chemistry , Nitrosomonas/enzymology , Amino Acid Sequence , Crystallization , Dimerization , Heme/chemistry , Ligands , Models, Molecular , Molecular Sequence Data , Peroxidases/chemistry , Protein Conformation , Protein Structure, Tertiary , Sequence Homology, Amino Acid
6.
Biochemistry ; 40(7): 2243-50, 2001 Feb 20.
Article in English | MEDLINE | ID: mdl-11329293

ABSTRACT

Manganese peroxidase (MnP) is a heme-containing enzyme produced by white-rot fungi and is part of the extracellular lignin degrading system in these organisms. MnP is unique among Mn binding enzymes in its ability to bind and oxidize Mn(II) and efficiently release Mn(III). Initial site-directed mutagenesis studies identified the residues E35, E39, and D179 as the Mn binding ligands. However, an E39D variant was recently reported to display wild-type Mn binding and rate of oxidation, calling into question the role of E39 as an Mn ligand. To investigate this hypothesis, we performed computer modeling studies which indicated metal-ligand bond distances in the E39D variant and in an E35D--E39D--D179E triple variant which might allow Mn binding and oxidation. To test the model, we reconstructed the E35D and E39D variants used in the previous study, as well as an E39A single variant and the E35D--E39D--D179E triple variant of MnP isozyme 1 from Phanerochaete chrysosporium. We find that all of the variant proteins are impaired for Mn(II) binding (K(m) increases 20--30-fold) and Mn(II) oxidation (k(cat) decreases 50--400-fold) in both the steady state and the transient state. In particular, mutation of the E39 residue in MnP decreases both Mn binding and oxidation. The catalytic efficiency of the E39A variants decreased approximately 10(4)-fold, while that of the E39D variant decreased approximately 10(3)-fold. Contrary to initial modeling results, the triple variant performed only as well as any of the single Mn ligand variants. Interestingly, the catalytic efficiency of the triple variant decreased only 10(4)-fold, which is approximately 10(2)-fold better than that reported for the E35Q--D179N double variant. These combined studies indicate that precise geometry of the Mn ligands within the Mn binding site of MnP is essential for the efficient binding, oxidation, and release of Mn by this enzyme. The results clearly indicate that E39 is a Mn ligand and that mutation of this ligand decreases both Mn binding and the rate of Mn oxidation.


Subject(s)
Glutamic Acid/metabolism , Manganese/metabolism , Peroxidases/metabolism , Phanerochaete/enzymology , Amino Acid Substitution/genetics , Aspartic Acid/genetics , Binding Sites/genetics , Computer Simulation , Kinetics , Models, Molecular , Mutagenesis, Site-Directed , Oxidation-Reduction , Peroxidases/biosynthesis , Peroxidases/genetics , Peroxidases/isolation & purification , Phanerochaete/genetics , Recombinant Proteins/biosynthesis , Recombinant Proteins/isolation & purification , Recombinant Proteins/metabolism , Sequence Analysis, DNA , Spectrophotometry, Ultraviolet
7.
Eur J Biochem ; 267(6): 1761-9, 2000 Mar.
Article in English | MEDLINE | ID: mdl-10712608

ABSTRACT

Inhibition of manganese peroxidase by cadmium was studied under steady-state and transient-state kinetic conditions. CdII is a reversible competitive inhibitor of MnII in the steady state with Ki approximately 10 microM. CdII also inhibits enzyme-generated MnIII-chelate-mediated oxidation of 2,6-dimethoxyphenol with Ki approximately 4 microM. CdII does not inhibit direct oxidation of phenols such as 2,6-dimethoxyphenol or guaiacol (2-methoxyphenol) in the absence of MnII. CdII alters the heme Soret on binding manganese peroxidase and exhibits a Kd approximately 8 microM, similar to Mn (Kd approximately 10 microM). Under transient-state conditions, CdII inhibits reduction of compound I and compound II by MnII at pH 4.5. However, CdII does not inhibit formation of compound I nor does it inhibit reduction of the enzyme intermediates by phenols in the absence of MnII. Kinetic analysis suggests that CdII binds at the MnII-binding site, preventing oxidation of MnII, but does not impair oxidation of substrates, such as phenols, which do not bind at the MnII-binding site. Finally, at pH 4.5 and 55 degrees C, MnII and CdII both protect manganese peroxidase from thermal denaturation more efficiently than CaII, extending the half-life of the enzyme by more than twofold. Furthermore, the combination of half MnII and half CdII nearly quadruples the enzyme half-life over either metal alone or either metal in combination with CaII.


Subject(s)
Cadmium/pharmacology , Enzyme Inhibitors/pharmacology , Fungal Proteins/antagonists & inhibitors , Manganese/metabolism , Peroxidases/antagonists & inhibitors , Binding Sites , Binding, Competitive , Cadmium/chemistry , Cadmium/metabolism , Calcium/metabolism , Enzyme Inhibitors/chemistry , Fungal Proteins/chemistry , Fungal Proteins/metabolism , Half-Life , Hot Temperature , Isoenzymes/antagonists & inhibitors , Isoenzymes/chemistry , Isoenzymes/metabolism , Kinetics , Oxidation-Reduction , Peroxidases/chemistry , Peroxidases/metabolism , Phanerochaete/enzymology , Protein Binding , Protein Denaturation/drug effects , Pyrogallol/analogs & derivatives , Pyrogallol/metabolism
8.
J Biol Chem ; 274(53): 37827-33, 1999 Dec 31.
Article in English | MEDLINE | ID: mdl-10608846

ABSTRACT

We have previously shown that the K(+) site found in ascorbate peroxidase can be successfully engineered into the closely homologous peroxidase, cytochrome c peroxidase (CCP) (Bonagura, C. A. , Sundaramoorthy, M., Pappa, H. S., Patterson, W. R., and Poulos, T. L. (1996) Biochemistry 35, 6107-6115; Bonagura, C. A., Sundaramoorthy, M., Bhaskar, B., and Poulos, T. L. (1999) Biochemistry 38, 5538-5545). All other peroxidases bind Ca(2+) rather than K(+). Using the K(+)-binding CCP mutant (CCPK2) as a template protein, together with observations from structural modeling, mutants were designed that should bind Ca(2+) selectively. The crystal structure of the first generation mutant, CCPCA1, showed that a smaller cation, perhaps Na(+), is bound instead of Ca(2+). This is probably because the full eight-ligand coordination sphere did not form owing to a local disordering of one of the essential cation ligands. Based on these observations, a second mutant, CCPCA2, was designed. The crystal structure showed Ca(2+) binding in the CCPCA2 mutant and a well ordered cation-binding loop with the full complement of eight protein to cation ligands. Because cation binding to the engineered loop results in diminished CCP activity and destabilization of the essential Trp(191) radical as measured by EPR spectroscopy, these measurements can be used as sensitive methods for determining cation-binding selectivity. Both activity and EPR titration studies show that CCPCA2 binds Ca(2+) more effectively than K(+), demonstrating that an iterative protein engineering-based approach is important in switching protein cation selectivity.


Subject(s)
Cytochrome-c Peroxidase/metabolism , Potassium/metabolism , Amino Acid Sequence , Base Sequence , Binding Sites , Crystallography, X-Ray , Cytochrome-c Peroxidase/chemistry , Cytochrome-c Peroxidase/genetics , DNA Primers , Electron Spin Resonance Spectroscopy , Kinetics , Models, Molecular , Mutagenesis, Site-Directed , Protein Engineering , Sequence Homology, Amino Acid
9.
Biochemistry ; 38(17): 5538-45, 1999 Apr 27.
Article in English | MEDLINE | ID: mdl-10220341

ABSTRACT

Earlier work [Bonagura et al. (1996) Biochemistry 35, 6107] showed that the K+ site found in the proximal pocket of ascorbate peroxidase (APX) could be engineered into cytochrome c peroxidase (CCP). Binding of K+ at the engineered site results in a loss in activity and destabilization of the CCP compound I Trp191 cationic radical owing to long-range electrostatic effects. The engineered CCP mutant crystal structure has been refined to 1.5 A using data obtained at cryogenic temperatures which provides a more detailed basis for comparison with the naturally occurring K+ site in APX. The characteristic EPR signal associated with the Trp191 radical becomes progressively weaker as K+ is added, which correlates well with the loss in enzyme activity as [K+] is increased. These results coupled with stopped-flow studies support our earlier conclusions that the loss in activity and EPR signal is due to destabilization of the Trp191 cationic radical.


Subject(s)
Cations/chemical synthesis , Cations/metabolism , Cytochrome-c Peroxidase/chemical synthesis , Cytochrome-c Peroxidase/metabolism , Recombinant Proteins/chemical synthesis , Recombinant Proteins/metabolism , Binding Sites/genetics , Crystallization , Crystallography, X-Ray , Electron Spin Resonance Spectroscopy , Enzyme Activation/genetics , Kinetics , Models, Molecular , Potassium/metabolism , Protein Engineering/methods , Structure-Activity Relationship
10.
Chem Biol ; 5(9): 461-73, 1998 Sep.
Article in English | MEDLINE | ID: mdl-9751642

ABSTRACT

BACKGROUND: Chloroperoxidase (CPO) is the most versatile of the known heme enzymes. It catalyzes chlorination of activated C-H bonds, as well as peroxidase, catalase and cytochrome P450 reactions, including enantioselective epoxidation. CPO contains a proximal heme-thiolate ligand, like P450, and polar distal pocket, like peroxidase. The substrate-binding site is formed by an opening above the heme that enables organic substrates to approach the activated oxoferryl oxygen atom. CPO, unlike other peroxidases, utilizes a glutamate acid-base catalyst, rather than a histidine residue. RESULTS: The crystal structures of CPO complexed with exogenous ligands, carbon monoxide, nitric oxide, cyanide and thiocyanate, have been determined. The distal pocket discriminates ligands on the basis of size and pKa. The refined CPO-ligand structures indicate a rigid active-site architecture with an immobile glutamate acid-base catalyst. Molecular modeling and dynamics simulations of CPO with the substrate cis-beta methylstyrene and the corresponding epoxide products provide a structural and energetic basis for understanding the enantioselectivity of CPO-catalyzed epoxidation reactions. CONCLUSIONS: The various CPO-ligand structures provide the basis for a detailed stereochemical mechanism of the formation of the intermediate compound I, in which Glu183 acts as an acid-base catalyst. The observed rigidity in the active site also explains the relative instability of CPO compound I and the formation of the HOCI chlorinating species. Energetics of CPO-substrate/ product molecular modeling provides a theoretical basis for the P450-type enantioselective epoxidation activities of CPO.


Subject(s)
Chloride Peroxidase/metabolism , Models, Chemical , Binding Sites , Catalysis , Crystallography, X-Ray , Epoxy Compounds/metabolism , Ferrous Compounds/metabolism , Fourier Analysis , Heme/metabolism , Ligands , Mitosporic Fungi/enzymology , Models, Molecular , Protein Binding , Protein Conformation , Stereoisomerism , Styrenes/metabolism
11.
J Biol Chem ; 272(28): 17574-80, 1997 Jul 11.
Article in English | MEDLINE | ID: mdl-9211904

ABSTRACT

Manganese peroxidase (MnP), an extracellular heme enzyme from the lignin-degrading basidiomycetous fungus, Phanerochaete chrysosporium, catalyzes the oxidation of MnII to MnIII. The latter, acting as a diffusible redox mediator, is capable of oxidizing a variety of lignin model compounds. The proposed MnII binding site of MnP consists of a heme propionate, three acidic ligands (Glu-35, Glu-39, and Asp-179), and two water molecules. Using crystallographic methods, this binding site was probed by altering the amount of MnII bound to the protein. Crystals grown in the absence of MnII, or in the presence of EDTA, exhibited diminished electron density at this site. Crystals grown in excess MnII exhibited increased electron density at the proposed binding site but nowhere else in the protein. This suggests that there is only one major MnII binding site in MnP. Crystal structures of a single mutant (D179N) and a double mutant (E35Q,D179N) at this site were determined. The mutant structures lack a cation at the MnII binding site. The structure of the MnII binding site is altered significantly in both mutants, resulting in increased access to the solvent and substrate.


Subject(s)
Peroxidases/genetics , Basidiomycota , Binding Sites/genetics , Crystallography, X-Ray , Edetic Acid/metabolism , Manganese/metabolism , Models, Chemical , Models, Molecular , Molecular Sequence Data , Mutagenesis, Site-Directed , Peroxidases/metabolism , Protein Conformation
12.
J Struct Biol ; 116(3): 429-31, 1996.
Article in English | MEDLINE | ID: mdl-8813001

ABSTRACT

The di-heme peroxidase (cytochrome c553 peroxidase) from Nitrosomonas europaea has been crystallized in a form suitable for high-resolution X-ray structure determination. A complete data set was obtained to 2.5A and the data were indexed in space group P2(1) with a = 88.79 A, b = 55.93 A, c = 144.37 A, beta = 103.87 degrees. The self-rotation function indicates one homodimer per asymmetric unit.


Subject(s)
Cytochrome-c Peroxidase/chemistry , Cytochrome-c Peroxidase/isolation & purification , Nitrosomonas/enzymology , Amino Acid Sequence , Crystallization , Crystallography, X-Ray , Heme , Molecular Sequence Data , Pseudomonas aeruginosa/enzymology , Sequence Homology, Amino Acid
13.
Biochemistry ; 35(19): 6107-15, 1996 May 14.
Article in English | MEDLINE | ID: mdl-8634253

ABSTRACT

The crystal structures of cytochrome c peroxidase and ascorbate peroxidase are very similar, including the active site architecture. Both peroxidases have a tryptophan residue, designated the proximal Trp, located directly adjacent to the proximal histidine heme ligand. During the catalytic cycle, the proximal Trp in cytochrome c peroxidase is oxidized to a cation radical. However, in ascorbate peroxidase, the porphyrin is oxidized, not the proximal Trp, despite the close similarity between the two peroxidase active site structures. A cation located approximately 8 A from the proximal Trp in ascorbate peroxidase but absent in cytochrome c peroxidase is thought to be one reason why ascorbate peroxidase does not form a Trp radical. Site-directed mutagenesis has been used to introduce the ascorbate peroxidase cation binding site into cytochrome c peroxidase. Crystal structures show that mutants now bind a cation. Electron paramagnetic resonance spectroscopy shows that the cation-containing mutants of cytochrome c peroxidase no longer form a stable Trp radical. The activity of the cation mutants using ferrocytochrome c as a substrate is < 1% of wild type levels, while the activity toward a small molecule substrate, guaiacol, increases. These results demonstrate that long range electrostatic effects can control the reactivity of a redox active amino acid side chain and that oxidation/reduction of the proximal Trp is important in the oxidation of ferrocytochrome c.


Subject(s)
Cytochrome-c Peroxidase/metabolism , Tryptophan/metabolism , Animals , Base Sequence , Cations , Crystallography, X-Ray , Cytochrome-c Peroxidase/chemistry , Cytochrome-c Peroxidase/genetics , Electron Spin Resonance Spectroscopy , Horses , Molecular Sequence Data , Oxidation-Reduction
14.
Structure ; 3(12): 1367-77, 1995 Dec 15.
Article in English | MEDLINE | ID: mdl-8747463

ABSTRACT

BACKGROUND: Chloroperoxidase (CPO) is a versatile heme-containing enzyme that exhibits peroxidase, catalase and cytochrome P450-like activities in addition to catalyzing halogenation reactions. The structure determination of CPO was undertaken to help elucidate those structural features that enable the enzyme to exhibit these multiple activities. RESULTS: Despite functional similarities with other heme enzymes, CPO folds into a novel tertiary structure dominated by eight helical segments. The catalytic base, required to cleave the peroxide O-O bond, is glutamic acid rather than histidine as in other peroxidases. CPO contains a hydrophobic patch above the heme that could be the binding site for substrates that undergo P450-like reactions. The crystal structure also shows extensive glycosylation with both N- and O-linked glycosyl chains. CONCLUSIONS: The proximal side of the heme in CPO resembles cytochrome P450 because a cysteine residue serves as an axial heme ligand, whereas the distal side of the heme is 'peroxidase-like' in that polar residues form the peroxide-binding site. Access to the heme pocket is restricted to the distal face such that small organic substrates can interact with the iron-linked oxygen atom which accounts for the P450-like reactions catalyzed by chloroperoxidase.


Subject(s)
Chloride Peroxidase/chemistry , Fungal Proteins/chemistry , Mitosporic Fungi/enzymology , Models, Molecular , Protein Structure, Tertiary , Amino Acid Sequence , Binding Sites , Catalysis , Computer Simulation , Crystallography, X-Ray , Cytochrome P-450 Enzyme System/chemistry , Glutamic Acid/chemistry , Glycosylation , Heme/chemistry , Hemeproteins/chemistry , Hemeproteins/classification , Hydrogen Bonding , Iron/chemistry , Molecular Sequence Data , Structure-Activity Relationship
15.
Acta Crystallogr D Biol Crystallogr ; 51(Pt 5): 842-4, 1995 Sep 01.
Article in English | MEDLINE | ID: mdl-15299822

ABSTRACT

Chloroperoxidase from the fungus Caldariomyces fumago has been crystallized in two space groups, C222(1) and P2(1)2(1)2(1) both of which are suitable for high-resolution X-ray studies. Parent data sets have been obtained to 2.16 A in space group C222(1) and 2.00 A in space group P2(1)2(1)2(1). Heavy-atom derivatives have been obtained with both forms and electron-density maps calculated. The heme has been located and continuous electron density between the heme and protein clearly indicates the location of the proximal ligand.

17.
J Biol Chem ; 269(52): 32759-67, 1994 Dec 30.
Article in English | MEDLINE | ID: mdl-7806497

ABSTRACT

The crystal structure of manganese peroxidase (MnP) from the lignin-degrading basidiomycetous fungus Phanerochaete chrysosporium has been solved using molecular replacement techniques and refined to R = 0.20 at 2.0 A. The overall structure is similar to that of two other fungal peroxidases, lignin peroxidase from P. chrysosporium and Arthromyces ramosus peroxidase. Like the other fungal peroxidases, MnP has two structural calcium ions. MnP also has two N-acetylglucosamine residues N-linked to Asn131 that are readily visible in the electron density map. The active site, consisting of a proximal His ligand H-bonded to an Asp residue and a distal side peroxide binding pocket consisting of a catalytic His and Arg, is the same as in the aforementioned fungal peroxidases as well as yeast cytochrome c peroxidase. MnP differs in having five rather than four disulfide bonds. The additional disulfide bond, Cys341-Cys348, is located near the C terminus of the polypeptide chain. Importantly, a new cation binding site, which we propose is the manganese-binding site of MnP, was located in the crystal structure. The ligands constituting the Mn(2+)-binding site include Asp179, Glu35, Glu39, a heme propionate, and two water molecules. Electron transfer from Mn2+ to the heme edge or iron center is envisioned to occur through a sigma-bonded pathway along a heme propionate.


Subject(s)
Basidiomycota/enzymology , Peroxidases/chemistry , Amino Acid Sequence , Binding Sites , Calcium/metabolism , Crystallography, X-Ray , Glycosylation , Models, Molecular , Molecular Sequence Data , Peroxidases/metabolism , Protein Conformation , Sequence Alignment
18.
J Biol Chem ; 269(32): 20239-49, 1994 Aug 12.
Article in English | MEDLINE | ID: mdl-8051115

ABSTRACT

The role of the proximal histidine ligand in peroxidase function was studied by replacing the His side chain in cytochrome c peroxidase with Gln, Glu, or Cys. In addition, a double mutant was prepared where His-175 is converted to Gln and the site of free radical formation in Compound I, Trp-191 (Sivaraja, M., Goodin, D.B., Smith, M., and Hoffman, B. M. (1989) Science 245, 738-740), is converted to Phe. With the exception of the His-175-->Cys mutant, the proximal ligand mutants retain high levels of enzyme activity. Stopped flow studies show that replacing the His ligand with Gln has only a modest effect on the rate of Compound I formation demonstrating that the precise nature of the proximal ligand is not important in achieving a high rate of peroxide O-O bond cleavage. The double mutant, His-175-->Gln/Trp-191-->Phe, also forms Compound I rapidly but the initial product formed is very likely a long-lived porphyrin pi cation radical that slowly converts to a species more closely resembling the heme oxyferryl center of wild type Compound I. The relevance of these studies to the cytochrome c peroxidase-cytochrome c electron transfer system are discussed.


Subject(s)
Cytochrome-c Peroxidase/metabolism , Crystallography, X-Ray , Cytochrome-c Peroxidase/chemistry , Cytochrome-c Peroxidase/genetics , Electron Spin Resonance Spectroscopy , Kinetics , Ligands , Mutagenesis, Site-Directed , Oxidation-Reduction
19.
J Mol Biol ; 238(5): 845-8, 1994 May 20.
Article in English | MEDLINE | ID: mdl-8182752

ABSTRACT

Manganese peroxidase from the white rot basidiomycete Phanerochaete chrysosporium has been crystallized in a form suitable for high-resolution X-ray structure determination. Crystals were grown from solutions containing 30% polyethylene glycol 8000, ammonium sulfate and cacodylate buffer at pH 6.5, using macroseeding techniques. A complete data set has been obtained to 2.06 A resolution. The data can be indexed in space group P1 with a = 45.96 A, b = 53.77 A, c = 84.87 A, alpha = 97.01 degrees, beta = 105.72 degrees and gamma = 90.1 degrees, with two peroxidase molecules per asymmetric unit, or in space group C2 with a = 163.23 A, b = 45.97 A, c = 53.72 A and beta = 97.16 degrees, with only one molecule in the assymetric unit. Lignin peroxidase, which shares about 57% sequence identity with manganese peroxidase, was used as a probe for molecular replacement. Unique rotation and translation solutions have been obtained in space groups P1 and C2. The structure has been partially refined in space group C2 to R = 0.22 for data between 10 and 2.06 A.


Subject(s)
Basidiomycota/enzymology , Peroxidases/chemistry , Crystallization , Crystallography, X-Ray , Molecular Structure , Peroxidases/genetics , Sequence Homology, Amino Acid
20.
J Biol Chem ; 267(36): 25656-9, 1992 Dec 25.
Article in English | MEDLINE | ID: mdl-1334481

ABSTRACT

Using site-directed mutagenesis, a double mutant in yeast cytochrome c peroxidase (CCP) has been constructed where the proximal ligand, His175, has been converted to glutamine and the neighboring Trp191 has been converted to phenylalanine. The refined 2.4-A crystal structure of the double mutant shows that the Gln175 side chain is within coordination distance of the heme iron atom and that Phe191 occupies the same position as Trp191 in the native enzyme with very little rearrangement outside the immediate vicinity of the mutations. Consistent with earlier work, we find that the single mutant, His175-->Gln, is fully active under steady state assay conditions and that as reported earlier (Mauro et al., 1988), the Trp191-->Phe mutant exhibits only < 0.05% activity. However, the double mutant, His175-->Gln/Phe191-->Phe, exhibits 20% wild type activity. Since it is known that the Trp191-->Phe mutant is inactive because it can no longer transfer electrons from ferrocytochrome c, changing the nature of the proximal ligand is able to restore this activity. These results raise interesting questions regarding the mechanism of interprotein electron transfer reactions.


Subject(s)
Cytochrome-c Peroxidase/genetics , Cytochrome-c Peroxidase/metabolism , Glutamine , Histamine , Mutagenesis, Site-Directed , Amino Acid Sequence , Cytochrome-c Peroxidase/chemistry , Ligands , Models, Molecular , Oxidation-Reduction , Protein Conformation , Recombinant Proteins/chemistry , Recombinant Proteins/metabolism , Spectrophotometry , Thermodynamics , X-Ray Diffraction
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