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2.
Biochemistry ; 40(18): 5422-32, 2001 May 08.
Article in English | MEDLINE | ID: mdl-11331006

ABSTRACT

Phosphatidylinositol-specific phospholipase C (PI-PLC) catalyzes the cleavage of the P-O bond in phosphatidylinositol via intramolecular nucleophilic attack of the 2-hydroxyl group of inositol on the phosphorus atom. Our earlier stereochemical and site-directed mutagenesis studies indicated that this reaction proceeds by a mechanism similar to that of RNase A, and that the catalytic site of PI-PLC consists of three major components analogous to those observed in RNase A, the His32 general base, the His82 general acid, and Arg69 acting as a phosphate-activating residue. In addition, His32 is associated with Asp274 in forming a catalytic triad with inositol 2-hydroxyl, and His82 is associated with Asp33 in forming a catalytic diad. The focus of this work is to provide a global view of the mechanism, assess cooperation between various catalytic residues, and determine the origin of enzyme activation by the hydrophobic leaving group. To this end, we have investigated kinetic properties of Arg69, Asp33, and His82 mutants with phosphorothioate substrate analogues which feature leaving groups of varying hydrophobicity and pK(a). Our results indicate that interaction of the nonbridging pro-S oxygen atom of the phosphate group with Arg69 is strongly affected by Asp33, and to a smaller extent by His82. This result in conjunction with those obtained earlier can be rationalized in terms of a novel, dual-function triad comprised of Arg69, Asp33, and His82 residues. The function of this triad is to both activate the phosphate group toward the nucleophilic attack and to protonate the leaving group. In addition, Asp33 and His82 mutants displayed much smaller degrees of activation by the fatty acid-containing leaving group as compared to the wild-type (WT) enzyme, and the level of activation was significantly reduced for substrates featuring the leaving group with low pK(a) values. These results strongly suggest that the assembly of the above three residues into the fully catalytically competent triad is controlled by the hydrophobic interactions of the enzyme with the substrate leaving group.


Subject(s)
Arginine/chemistry , Asparagine/chemistry , Catalytic Domain , Histidine/chemistry , Organophosphates/chemistry , Type C Phospholipases/chemistry , Amino Acid Substitution/genetics , Arginine/genetics , Asparagine/genetics , Bacillus cereus/enzymology , Binding Sites/genetics , Catalysis , Catalytic Domain/genetics , Histidine/genetics , Hydrolysis , Inositol Phosphates/chemistry , Phosphatidylinositol Diacylglycerol-Lyase , Phosphoinositide Phospholipase C , Ribonuclease, Pancreatic/chemistry , Glycine max/enzymology , Structure-Activity Relationship , Substrate Specificity/genetics , Sulfur/chemistry , Thionucleotides/chemistry , Type C Phospholipases/genetics
3.
J Biol Chem ; 276(19): 15823-31, 2001 May 11.
Article in English | MEDLINE | ID: mdl-11278668

ABSTRACT

Selenoprotein P is a plasma protein that has oxidant defense properties. It binds to heparin at pH 7.0, but most of it becomes unbound as the pH is raised to 8.5. This unusual heparin binding behavior was investigated by chemical modification of the basic amino acids of the protein. Diethylpyrocarbonate (DEPC) treatment of the protein abolished its binding to heparin. DEPC and [(14)C]DEPC modification, coupled with amino acid sequencing and matrix-assisted laser desorption ionization-time of flight mass spectrometry of peptides, identified several peptides in which histidine and lysine residues had been modified by DEPC. Two peptides from one region (residues 80-95) were identified by both methods. Moreover, the two peptides that constituted this sequence bound to heparin. Finally, when DEPC modification of the protein was carried out in the presence of heparin, these two peptides did not become modified by DEPC. Based on these results, the heparin-binding region of the protein sequence was identified as KHAHLKKQVSDHIAVY. Two other peptides (residues 178-189 and 194-234) that contain histidine-rich sequences met some but not all of the criteria of heparin-binding sites, and it is possible that they and the histidine-rich sequence between them bind to heparin under some conditions. The present results indicate that histidine is a constituent of the heparin-binding site of selenoprotein P. The presence of histidine, the pK(a) of which is 7.0, explains the release of selenoprotein P from heparin binding as pH rises above 7.0. It can be speculated that this property would lead to increased binding of selenoprotein P in tissue regions that have low pH.


Subject(s)
Heparin/metabolism , Histidine , Lysine , Proteins/chemistry , Proteins/metabolism , Amino Acid Sequence , Animals , Binding Sites , Carbon Radioisotopes , Chromatography, Affinity , Chromatography, High Pressure Liquid , Diethyl Pyrocarbonate/pharmacokinetics , Diethyl Pyrocarbonate/pharmacology , Hydrogen-Ion Concentration , Molecular Sequence Data , Peptide Fragments/chemistry , Proteins/isolation & purification , Rats , Selenoprotein P , Selenoproteins , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
4.
Arch Biochem Biophys ; 371(1): 29-34, 1999 Nov 01.
Article in English | MEDLINE | ID: mdl-10525286

ABSTRACT

Selenomethionine has been suggested to protect against peroxynitrite by quenching it in vivo. Selenomethionine is distributed randomly in the methionine pool. Albumin and IgG were purified from plasma of a human being before and after 28 days of supplementation with 400 microg selenium/day as selenomethionine. The albumin contained 1 selenium atom, presumably as selenomethionine, per 8000 methionine residues before supplementation and 1 per 2800 after supplementation. Although this ratio suggested that selenomethionine would not have as great an effect in quenching peroxynitrite as would methionine, direct testing of the albumin and IgG fractions was carried out to assess the ability of these proteins to prevent peroxynitrite oxidation of dihydrorhodamine 123 to rhodamine 123. The ability of the albumin preparations to resist nitration of tyrosine residues was also assessed. The high-selenomethionine preparations of the proteins had no greater effect in quenching the peroxynitrite than did the normal-selenomethionine preparations. These results do not support the proposal that selenomethionine in proteins contributes to in vivo protection against peroxynitrite.


Subject(s)
Immunoglobulin G/chemistry , Nitrates/pharmacology , Oxidants/pharmacology , Selenium/pharmacokinetics , Selenomethionine , Serum Albumin/chemistry , Adult , Humans , Immunoglobulin G/drug effects , Male , Oxidation-Reduction , Serum Albumin/drug effects
5.
Biochemistry ; 37(13): 4568-80, 1998 Mar 31.
Article in English | MEDLINE | ID: mdl-9521777

ABSTRACT

The mechanism of phosphatidylinositol-specific phospholipase C (PI-PLC) has been suggested to resemble that of ribonuclease A. The goal of this work is to rigorously evaluate the mechanism of PI-PLC from Bacillus thuringiensis by examining the functional and structural roles of His-32 and His-82, along with the two nearby residues Asp-274 and Asp-33 (which form a hydrogen bond with His-32 and His-82, respectively), using site-directed mutagenesis. In all, twelve mutants were constructed, which, except D274E, showed little structural perturbation on the basis of 1D NMR and 2D NOESY analyses. The H32A, H32N, H32Q, H82A, H82N, H82Q, H82D, and D274A mutants showed a 10(4)-10(5)-fold decrease in specific activity toward phosphatidylinositol; the D274N, D33A, and D33N mutants retained 0. 1-1% activity, whereas the D274E mutant retained 13% activity. Steady-state kinetic analysis of mutants using (2R)-1, 2-dipalmitoyloxypropane-3-(thiophospho-1d-myo-inositol) (DPsPI) as a substrate generally agreed well with the specific activity toward phosphatidylinositol. The results suggest a mechanism in which His-32 functions as a general base to abstract the proton from 2-OH and facilitates the attack of the deprotonated 2-oxygen on the phosphorus atom. This general base function is augmented by the carboxylate group of Asp-274 which forms a diad with His-32. The H82A and D33A mutants showed an unusually high activity with substrates featuring low pKa leaving groups, such as DPsPI and p-nitrophenyl inositol phosphate (NPIPs). These results suggest that His-82 functions as the general acid with assistance from Asp-33, facilitating the departure of the leaving group by protonation of the glycerol O3 oxygen. The Bronsted coefficients obtained for the WT and the D33N mutant indicate a high degree of proton transfer to the leaving group and further underscore the "helper" function of Asp-33. The complete mechanism also includes activation of the phosphate group toward nucleophilic attack by a hydrogen bond between Arg-69 and a nonbridging oxygen atom. The overall mechanism can be described as "complex" general acid-general base since three elements are required for efficient catalysis.


Subject(s)
Type C Phospholipases/metabolism , Alcohols/metabolism , Aspartic Acid/genetics , Aspartic Acid/metabolism , Binding Sites , Catalysis , Circular Dichroism , Escherichia coli/metabolism , Esterification , Guanidine , Histidine/genetics , Histidine/metabolism , Inositol Phosphates/metabolism , Kinetics , Mutagenesis, Site-Directed , Nuclear Magnetic Resonance, Biomolecular , Phosphatidylinositol Diacylglycerol-Lyase , Phosphatidylinositols/metabolism , Phosphoinositide Phospholipase C , Protein Conformation , Protein Denaturation , Recombinant Proteins/biosynthesis , Recombinant Proteins/chemistry , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Type C Phospholipases/biosynthesis , Type C Phospholipases/chemistry , Type C Phospholipases/genetics
6.
Biochemistry ; 36(22): 6633-42, 1997 Jun 03.
Article in English | MEDLINE | ID: mdl-9184143

ABSTRACT

A new substrate analogue, (2R)-1,2-dipalmitoyloxypropanethiophospho-1-D-myo-inositol (DPsPI), has been used in a new, continuous assay for phosphatidylinositol-specific phospholipase C (PI-PLC). DPsPI is superior to other substrate analogs that have been used for assaying PI-PLC since it is synthesized as a pure diastereomer and maintains both acyl chains of the natural substrate, dipalmitoylphosphatidylinositol (DPPI). The assay that has been developed using this new analogue has allowed us to elucidate detailed kinetic data so far lacking in the field. In addition, several mutants of PI-PLC were constructed and assayed. The results show that Arg-69 is essential for catalysis, since mutations at this position led to a 10(3)- 10(4)-fold decrease in activity with respect that of to the wild-type (WT) enzyme. An alanine mutant of Asp-67, a residue also found at the active site, displays activity similar to that of WT. We have also used nuclear magnetic resonance (NMR) and circular dichroism (CD) spectroscopy to analyze the structural integrity and conformational stability of the mutants. The results show that the overall global conformation of the enzyme is not perturbed by the mutants. The 15N-1H HSQC NMR spectrum of WT PI-PLC is also reported at 600 MHz. The stereoselectivity of the reaction toward the stereoisomers of another analogue, 1,2-dipalmitoyl-sn-glycero-3-thiophospho-1-myo-inositol (DPPsI), was used to probe whether Arg-69 interacts with the phosphate moiety of the substrate. We have calculated that the WT enzyme shows a stereoselectivity ratio of 160000:1 in favor of the Rp isomer versus the Sp isomer. The R69K mutant displayed a significant 10(4)-fold relaxation of stereoselectivity. Our data support the role of Arg-69 in stabilizing the negative charge on the pentacoordinate phosphate in the transition state during catalysis.


Subject(s)
Arginine/metabolism , Phosphates/metabolism , Phosphatidylinositols/chemistry , Phosphoric Diester Hydrolases/chemistry , Phosphoric Diester Hydrolases/metabolism , Bacillus thuringiensis/enzymology , Binding Sites , Catalysis , Circular Dichroism , Escherichia coli/genetics , Gene Expression , Kinetics , Magnetic Resonance Spectroscopy , Mutagenesis , Organothiophosphates/chemistry , Organothiophosphates/metabolism , Phosphatidylinositol Diacylglycerol-Lyase , Phosphatidylinositols/metabolism , Phosphoinositide Phospholipase C , Phosphoric Diester Hydrolases/genetics , Protein Conformation , Recombinant Proteins , Stereoisomerism , Structure-Activity Relationship , Thermodynamics
7.
Biochemistry ; 35(22): 7041-50, 1996 Jun 04.
Article in English | MEDLINE | ID: mdl-8679529

ABSTRACT

DNA polymerase beta (pol beta) is the smallest and least complex DNA polymerase. The structure of the enzyme is well understood, but little is known about its catalytic properties, particularly processivity and fidelity. Pre-steady-state analysis of the incorporation of a single nucleotide into a short 25/45 oligonucleotide primer-template by pol beta was used to define the kinetic parameters of the polymerase. In addition, nucleotide analogs and site-specific mutants, along with structural analyses, were used to probe the structure-function relationship of pol beta. Several significant findings have been obtained: (i) The catalysis by pol beta is processive and displays an initial burst under pre-steady-state conditions, but the processivity is poor compared to other polymerases. (ii) The fidelity of pol beta is also low relative to other polymerases. (iii) Under pre-steady-state conditions the chemical step appears to be only partially rate-limiting on the basis of the low thio effect (4.3), defined as kpol(dNTP)/kpol(dNTP alpha S). The thio effect increases to 9 for incorporation of an incorrect nucleotide. These results are consistent with the existence of a substrate-induced conformational change that is also partially rate-limiting. (iv) A comparison between the two-dimensional NMR spectra of the wild-type and mutant enzymes indicates that the mutations at position 283 did not significantly perturb the structure of the enzyme. The conformational stability of the mutants is also unperturbed. Thus, R283 is not important to the overall structure of the enzyme. (v) The results of kinetic analyses of R283A and R283K mutants indicate that the hydrogen bond between R283 of pol beta and the template is important for catalysis. Both R283A and R283K mutants displayed decreases in catalytic efficiency by a factor of ca. 200 relative to wild-type pol beta. The mutants are also less faithful by a factor of 2-4, in terms of the T-G mispair vs the T-A correct pair. The perturbation, however, could occur at both the implied conformational step and the chemical step, since the thio effects of the mutants for both correct and incorrect nucleotides are similar to those of WT pol beta.


Subject(s)
Arginine/chemistry , DNA Polymerase I/chemistry , DNA Polymerase I/metabolism , Protein Conformation , Animals , Arginine/metabolism , Base Sequence , Brain/metabolism , Catalysis , Circular Dichroism , Cloning, Molecular , Deoxyribonucleotides/metabolism , Escherichia coli/genetics , Guanidine , Guanidines , Kinetics , Magnetic Resonance Spectroscopy , Molecular Sequence Data , Mutagenesis, Site-Directed , Protein Denaturation , Rats , Rats, Sprague-Dawley , Thermodynamics
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