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J Inorg Biochem ; 104(2): 118-25, 2010 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-19926138

RESUMO

Modulations of protein-protein interactions are a key step in regulating protein function, especially in networks. Modulators of these interactions are supposed to be candidates for the development of novel drugs. Here, we describe the role of the small, polycationic and highly abundant natural polyamines that could efficiently bind to charged spots at protein interfaces as modulators of such protein-protein interactions. Using the mitochondrial cytochrome P45011A1 (CYP11A1) electron transfer system as a model, we have analyzed the capability of putrescine, spermidine, and spermine at physiologically relevant concentrations to affect the protein-protein interactions between adrenodoxin reductase (AdR), adrenodoxin (Adx), and CYP11A1. The actions of polyamines on the individual components, on their association/dissociation, on electron transfer, and on substrate conversion were examined. These studies revealed modulating effects of polyamines on distinct interactions and on the entire system in a complex way. Modulation via changed protein-protein interactions appeared plausible from docking experiments that suggested favourable high-affinity binding sites of polyamines (spermine>spermidine>putrescine) at the AdR-Adx interface. Our findings imply for the first time that small endogenous compounds are capable of interfering with distinct components of transient protein complexes and might control protein functions by modulating electrostatic protein-protein interactions.


Assuntos
Poliaminas/química , Poliaminas/farmacologia , Proteínas/química , Adrenodoxina/química , Adrenodoxina/genética , Adrenodoxina/metabolismo , Animais , Sítios de Ligação , Ligação Competitiva/efeitos dos fármacos , Catálise/efeitos dos fármacos , Enzima de Clivagem da Cadeia Lateral do Colesterol/química , Enzima de Clivagem da Cadeia Lateral do Colesterol/metabolismo , Transporte de Elétrons/efeitos dos fármacos , Ferredoxina-NADP Redutase/química , Ferredoxina-NADP Redutase/metabolismo , Humanos , Cinética , Modelos Moleculares , Mutação , Oxirredução/efeitos dos fármacos , Poliaminas/metabolismo , Ligação Proteica/efeitos dos fármacos , Estrutura Terciária de Proteína , Proteínas/metabolismo , Putrescina/química , Putrescina/metabolismo , Putrescina/farmacologia , Espermidina/química , Espermidina/metabolismo , Espermidina/farmacologia , Espermina/química , Espermina/metabolismo , Espermina/farmacologia , Eletricidade Estática
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