Ubago-Rodríguez, A., Casares Atienza, S., Fernández-Vivas, A., Peigneux, A., Jabalera, Y., de la Cuesta-Rivero, M., Jimenez-Lopez, C., & Azuaga Fortes, A.I. (2019) "Structure–Function of MamC Loop and Its Effect on the in Vitro Precipitation of Biomimetic Magnetite Nanoparticles." Crystal Growth & Design, 19 (5), 2927-2935. DOI: 10.1021/acs.cgd.9b00150Portada revista


Ana Dolores Ubago Rodríguez, Salvador Casares
Atienza, Antonia Fernández-Vivas, Ana Peigneux Navarro, Ylenia Jabalera
Ruz, Mario de la Cuesta Rivero, Concepción Jiménez López y Ana Isabel
Azuaga Fortes.


MamC, an integral protein of the magnetosome membrane, has recently been proposed as a strong candidate to produce biomimetic (magnetosome-like) magnetite nanoparticles that could be used as an alternative to magnetosomes in different applications such as nanocarriers. The secondary structure of the protein contains two helical transmembrane domains connected by an α-helical loop oriented toward the magnetosome lumen. In this loop, the residues Glu66 and Asp70 seem to be responsible for a template effect that controls the nucleation and/or growth of biomimetic nanoparticles in vitro. In the present study, we have introduced a double mutation, E66A and D70A, in the sequence of MamC while working, for the first time, with the full-length protein. Our results show that this doublé mutation does not affect either the conformation or the stability of MamC, but it indeed makes the protein lose its functionality in terms of controlling the process of magnetite biomineralization in vitro. The present study shows that the ionotropic effect is not enough to account for the effect of the wild type MamC on the formation of BMNPs, but the template effect seems to rule such a process. Also, it shows that no other region of MamC is involved in controlling the process of magnetite biomineralization. Moreover, the stability of MamC in solution is only marginal, probably due to the absence of contacts established with the membrane lipid bilayer.


La biomimética es una alternativa seguida para conseguir aumentar la producción de nanopartículas magnéticas. Para ello, se utilizan proteínas recombinantes específicas del magnetosoma cuya expresión y purificación se realiza a partir de un microorganismo de crecimiento conocido. En este artículo, conseguimos avanzar en el conocimiento de la conformación y función de una de las proteínas más abundantes, conocida como MamC. Concretamente, demostramos la importancia de dos aminoácidos localizados en el “loop” de la proteína, los cuales resultan esenciales para que la misma desarrolle su actividad de biomineralización *in vitro*.


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Nuestro grupo, perteneciente a la Facultad de Ciencias de la Universidad de Granada y supervisado por la Dra Concepción Jiménez López, se centra en el estudio de la producción de nanopartículas magnéticas biomiméticas de tipo magnetosoma mediante el uso de proteínas recombinantes específicas del mismo. Dentro de esto, nos centramos en la caracterización tanto de las proteínas como de dichas nanopartículas para poder funcionalizarlas con el fin de ser usadas como nanotransportadores inteligentes para una quimioterapia dirigida así como para tratamientos de hipertermia y otras aplicaciones, tanto clínicas como ambientales.

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