RESUMO
The cDNA encoding human cytosolic phospholipase A2 (cPLA2) has been subcloned into a prokaryotic pET16b expression vector which also encodes an amino-terminal deca-histidine affinity tag to facilitate purification of the recombinant enzyme. Soluble, active fusion protein, designated His-cPLA2, has been obtained reproducibly from this expression system using the E. coli strain BL21 (DE3). The protein has been purified to homogeneity in four steps and the mass confirmed by electrospray mass spectrometry. His-cPLA2 was characterized by kinetic analysis which demonstrated that the enzyme is similar to native cPLA2 in all respects investigated. Specifically, the enzyme binds to anionic vesicles containing substrate, and acts processively on these vesicles. Enzymatic activity is supported by the presence of Ca2+ and several other divalent metal ions, and is inhibited by several transition metal ions. Finally, the enzyme demonstrates lysophospholipase activity and exhibits a high selectivity for sn-2 arachidonyl esters. This prokaryotic expression system yields moderate amounts of unmodified recombinant His-cPLA2 and is advantageous for rapid production of protein and mutational analyses.
Assuntos
Fosfolipases A/metabolismo , Sequência de Aminoácidos , Sequência de Bases , Cálcio/farmacologia , Cátions Bivalentes/farmacologia , Cátions Monovalentes/farmacologia , Clonagem Molecular , Citosol/enzimologia , Primers do DNA , DNA Complementar/metabolismo , Ácido Edético/farmacologia , Escherichia coli , Expressão Gênica , Glicerol/farmacologia , Humanos , Cinética , Dados de Sequência Molecular , Fosfolipases A/biossíntese , Fosfolipases A/isolamento & purificação , Fosfolipases A2 , Reação em Cadeia da Polimerase , Proteínas Recombinantes de Fusão/biossíntese , Proteínas Recombinantes de Fusão/isolamento & purificação , Proteínas Recombinantes de Fusão/metabolismo , Especificidade por SubstratoRESUMO
This chapter has presented the basic methods involved in the use of 31P NMR to study positional isotope exchange in enzyme-catalyzed reactions involving phosphorus-containing substrates. The method is straightforward but requires synthesis of specific 18O isotopically labeled substrates at the site of bond cleavage. Analysis of the kinetic consequences of the PIX reaction depends on the nature of the enzymatic reaction and the number of other substrates involved in the kinetic reaction mechanism. This may be simple or formidable. From the examples described in this article one can appreciate that PIX experiments, when combined with other kinetic methods, can in favorable cases unravel many (if not all) of the rate constants in an enzyme-catalyzed reaction.
Assuntos
Espectroscopia de Ressonância Magnética/métodos , Compostos Organofosforados , Fosfatos , Fósforo , Monofosfato de Adenosina , Trifosfato de Adenosina , Marcação por Isótopo/métodos , Cinética , Isótopos de Oxigênio , Uridina TrifosfatoRESUMO
A number of complex biochemical problems have been solved recently by application of new techniques in which 31P and 13C NMR spectroscopy is used. Oxygen isotope exchange phenomena were studied by these NMR methods and used to analyze individual mechanistic events in enzymatic reactions. The existence of intermediates in the reactions catalyzed by glutamine synthetase (EC 6.3.1.2) and carbamyl-phosphate synthetase (EC 2.7.2.9) has been established as well as the kinetic competence of these intermediates for each enzyme. The NMR theory and kinetic experiments required to conduct such studies are discussed.