Respective roles of organic and mineral components of human cortical bone matrix in micromechanical behavior: An instrumented indentation study

International audienceBone is a multiscale composite material made of both a type I collagen matrix and a poorly crystalline apatite mineral phase. Due to remodeling activity, cortical bone is made of Bone Structural Units (BSUs) called osteons. Since osteon represents a fundamental level of structural hierarchy, it is important to investigate the relationship between mechanical behavior and tissue composition at this scale for a better understanding of the mechanisms of bone fragility. The aim of this study is to analyze the links between ultrastructural properties and the mechanical behavior of bone tissue at the scale of osteon. Iliac bone biopsies were taken from untreated postmenopausal osteoporotic women, embedded, sectioned and microradiographed to assess the degree of mineralization of bone (DMB). On each section, BSUs of known DMB were indented with relatively high load (∼500 mN) to determine local elastic modulus (E), contact hardness (Hc) and true hardness(H) of several bone lamellae. Crystallinity and collagen maturity were measured by Fourier Transform InfraRed Microspectroscopy (FTIRM) on the same BSUs. Inter-relationships between mechanical properties and ultrastructural components were analyzed using multiple regression analysis. This study showed that elastic deformation was only explained by DMB whereas plastic deformation was more correlated with collagen maturity. Contact hardness, reflecting both elastic and plastic behaviors, was correlated with both DMB and collagen maturity. Norelationship was found between crystallinity and mechanical properties at the osteon level

Evidence for the formation of distorted nanodomains involved in the phase transformation of stabilized zirconia by coupling convergent beam electron diffraction and in situ TEM nanoindentation

International audienceThe transformation of zirconia from its tetragonal to its monoclinic phase is an important feature of the zirconia system. First found to be an advantage due to its important toughening effect, it can also be very detrimental when it occurs in the framework of low-temperature degradation, particularly in the case of biomaterial applications. One way to avoid or to control this phase transformation is to understand how it initiates and more particularly the stress states that can trigger it. A new technique available inside a transmission electron microscope seems to be particularly well suited for that type of study: convergent beam electron diffraction, a well-known technique to reveal stresses, was coupled to in situ transmission electron microscopy mechanical nanoindentation. The experiments reveal the presence of sheared nanoregions at grain boundaries. These could act as embryos for tetragonal-to-monoclinic phase transformations. This is an important first step in the understanding of the earliest stage of zirconia phase transformation

Effect of amount of doping agent on sintering, microstructure and optical properties of Zr- and La-doped alumina sintered by SPS

SPS-produced α-alumina samples are prepared from powders doped with different amounts of Zr4+ and La3+ cations. Zr4+ cations segregate at grain boundaries. m-ZrO2 particles are formed at 570 but not at 280 cat ppm. A β-alumina LaAl11O18 structure is found at 310 cat ppm when the lanthanum grain boundary solubility limit is exceeded (∼200 cat ppm). 100 cat ppm La is sufficient to block the diffusion path across grain boundaries and inhibit grain growth. Both doping cations disturb the grain boundary diffusion whatever their amount. They delay the densification at higher temperatures while limiting grain growth. The real in-line transmittance (RIT) of α-alumina is improved due to the reduced grain size. Nevertheless, increasing the cation amount leads to an increase in porosity or even the formation of secondary phase particles, both detrimental for optical properties. Finally, optimised amounts of cation of 200 and 150 cat ppm are found for La- and Zr-doped alumina, respectively

Investigating the n- and p-Type Electrolytic Charging of Colloidal Nanoplatelets

We investigate the ion gel gating of 2D colloidal nanoplatelets. We propose a simple, versatile, and air-operable strategy to build electrolyte-gated transistors. We provide evidence that the charges are injected in the quantum states of the nanocrystals. The gating is made possible by the presence of large voids into the NPL films and is sensitive to the availability of the nanocrystals surface

Investigating the n- and p-Type Electrolytic Charging of Colloidal Nanoplatelets

We investigate the ion gel gating of 2D colloidal nanoplatelets. We propose a simple, versatile, and air-operable strategy to build electrolyte-gated transistors. We provide evidence that the charges are injected in the quantum states of the nanocrystals. The gating is made possible by the presence of large voids into the NPL films and is sensitive to the availability of the nanocrystals surface

Heterologous Expression of Membrane Proteins: Choosing the Appropriate Host

International audienceBACKGROUND: Membrane proteins are the targets of 50% of drugs, although they only represent 1% of total cellular proteins. The first major bottleneck on the route to their functional and structural characterisation is their overexpression; and simply choosing the right system can involve many months of trial and error. This work is intended as a guide to where to start when faced with heterologous expression of a membrane protein. METHODOLOGY/PRINCIPAL FINDINGS: The expression of 20 membrane proteins, both peripheral and integral, in three prokaryotic (E. coli, L. lactis, R. sphaeroides) and three eukaryotic (A. thaliana, N. benthamiana, Sf9 insect cells) hosts was tested. The proteins tested were of various origins (bacteria, plants and mammals), functions (transporters, receptors, enzymes) and topologies (between 0 and 13 transmembrane segments). The Gateway system was used to clone all 20 genes into appropriate vectors for the hosts to be tested. Culture conditions were optimised for each host, and specific strategies were tested, such as the use of Mistic fusions in E. coli. 17 of the 20 proteins were produced at adequate yields for functional and, in some cases, structural studies. We have formulated general recommendations to assist with choosing an appropriate system based on our observations of protein behaviour in the different hosts. CONCLUSIONS/SIGNIFICANCE: Most of the methods presented here can be quite easily implemented in other laboratories. The results highlight certain factors that should be considered when selecting an expression host. The decision aide provided should help both newcomers and old-hands to select the best system for their favourite membrane protein