Mixts. contg. water, lysozyme (LYS), and a fluorinated surfactant (LiPFN) have been investigated in a wide range of protein-to-surfactant ratios. Depending on compn., sample consistency and coexistence of the different phases, different exptl. methods were used. Volumetric, viscometric, surface tension, potentiometric (by a home-built ion-selective electrode), turbidity, optical polarizing microscopy, and 19F NMR expts. were used. The results obtained from the above methods have been interpreted in terms of a combination of electrostatic and hydrophobic contributions to the stability of the different phases formed in the water-LYS-LiPFN system. Solns., gel phases, and ppts. have been obsd. in the range investigated in more detail. Multiphase regions have also been obsd. Such rich polymorphic behavior implies the existence of interactions between the protein and surfactant. The gel phase is presumably formed by interconnections between micelles and protein-surfactant complexes, held together by protein-bound micelles and forming, presumably, interconnected necklace structures. The overlapping of different protein-surfactant aggregates to form gels requires a significant amt. of time. Its formation obeys a vol. fraction statistics; the width of the gel phase, in fact, is controlled by the amt. of protein-surfactant complex.
Supramolecular Association in the System Water – Lysozime - Lithium Perfluorononanoate / Sesta, B.; Gente, G.; Iovino, A.; Laureti, F.; Michiotti, P.; Paiusco, O.; Palacios, A. C.; Persi, L.; Princi, A.; Sallustio, S.; SARNTHEIN GRAF, C.; Capalbi, A.; LA MESA, Camillo. - In: JOURNAL OF PHYSICAL CHEMISTRY. B, CONDENSED MATTER, MATERIALS, SURFACES, INTERFACES & BIOPHYSICAL. - ISSN 1520-6106. - STAMPA. - 108:(2004), pp. 3036-3043.
Supramolecular Association in the System Water – Lysozime - Lithium Perfluorononanoate
LA MESA, Camillo
2004
Abstract
Mixts. contg. water, lysozyme (LYS), and a fluorinated surfactant (LiPFN) have been investigated in a wide range of protein-to-surfactant ratios. Depending on compn., sample consistency and coexistence of the different phases, different exptl. methods were used. Volumetric, viscometric, surface tension, potentiometric (by a home-built ion-selective electrode), turbidity, optical polarizing microscopy, and 19F NMR expts. were used. The results obtained from the above methods have been interpreted in terms of a combination of electrostatic and hydrophobic contributions to the stability of the different phases formed in the water-LYS-LiPFN system. Solns., gel phases, and ppts. have been obsd. in the range investigated in more detail. Multiphase regions have also been obsd. Such rich polymorphic behavior implies the existence of interactions between the protein and surfactant. The gel phase is presumably formed by interconnections between micelles and protein-surfactant complexes, held together by protein-bound micelles and forming, presumably, interconnected necklace structures. The overlapping of different protein-surfactant aggregates to form gels requires a significant amt. of time. Its formation obeys a vol. fraction statistics; the width of the gel phase, in fact, is controlled by the amt. of protein-surfactant complex.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.