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FEBS J ; 283(6): 1124-38, 2016 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-26785700

RESUMEN

Network structural analysis, known as residue interaction networks or graphs (RIN or RIG, respectively) or protein structural networks or graphs (PSN or PSG, respectively), comprises a useful tool for detecting important residues for protein function, stability, folding and allostery. In RIN, the tertiary structure is represented by a network in which residues (nodes) are connected by interactions (edges). Such structural networks have consistently presented a few central residues that are important for shortening the pathways linking any two residues in a protein structure. To experimentally demonstrate that central residues effectively participate in protein properties, mutations were directed to seven central residues of the ß-glucosidase Sfßgly (ß-D-glucoside glucohydrolase; EC 3.2.1.21). These mutations reduced the thermal stability of the enzyme, as evaluated by changes in transition temperature (Tm ) and the denaturation rate at 45 °C. Moreover, mutations directed to the vicinity of a central residue also caused significant decreases in the Tm of Sfßgly and clearly increased the unfolding rate constant at 45 °C. However, mutations at noncentral residues or at surrounding residues did not affect the thermal stability of Sfßgly. Therefore, the data reported in the present study suggest that the perturbation of the central residues reduced the stability of the native structure of Sfßgly. These results are in agreement with previous findings showing that networks are robust, whereas attacks on central nodes cause network failure. Finally, the present study demonstrates that central residues underlie the functional properties of proteins.


Asunto(s)
Proteínas/química , Sustitución de Aminoácidos , Animales , Dicroismo Circular , Estabilidad de Enzimas , Calor , Proteínas de Insectos/química , Proteínas de Insectos/genética , Proteínas de Insectos/metabolismo , Modelos Moleculares , Mutagénesis Sitio-Dirigida , Conformación Proteica , Desnaturalización Proteica , Pliegue de Proteína , Mapas de Interacción de Proteínas , Proteínas/genética , Proteínas/metabolismo , Espectrometría de Fluorescencia , Spodoptera/enzimología , Spodoptera/genética , beta-Glucosidasa/química , beta-Glucosidasa/genética , beta-Glucosidasa/metabolismo
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