WTC2005-63696 FRICTION AND WEAR BEHAVIOR OF BORONIZED CHROMIUM FOR BIOLOGICAL APPLICATIONS

ABSTRACT Enhanced corrosion and wear resistance are crucially important to prolong the service life of biomaterials. Boronizing has been reported to enhance the wear resistance of pure chromium. In this research, we investigate friction and wear behavior of boronized chromium. Pin-on-disc tribometer was used to conduct the wear and friction tests. Experiments were conducted in dry conditions as well as in simulated body fluid (SBF). Fundamental aspects of wear mode and lubrication behavior were studied using surface characterization techniques such as TEM, and X-ray diffraction. Results showed evidence of tribo-chemical interactions between SBF and work piece materials. INTRODUCTION Boride coatings have been applied to metal surfaces in order to improve their corrosion resistance, electrochemical properties, tribological performance, and to prolong service life [1, 2, 3 and 4]. Boronizing is one way to form this uniform coating on the substrate material. It is a thermo-chemical diffusion surface treatment in which boron atoms diffuse into the surface of the work piece to form hard borides with the base material

Phytoremediation of light non-aqueous phase liquids

Non-aqueous phase liquids (NAPLs) are persistent sources of contamination in the ground, providing a long-term supply of dissolved phase contamination and taking significant periods to dissipate naturally. Light NAPLs (LNAPLs) take the form of a separate phase within the ground, often as individual ganglia in pore spaces within the capillary zone such that the contaminated region is diffuse and comprised of many unconnected small contaminant sources. Consequently, remedial action is challenging and success may be limited to ex-situ remediation techniques. The ability of plants to phytoremediate dissolved-phase contamination is well known, but the impact of LNAPLs on plant growth and subsequent contaminant behaviour is largely unknown. Experimental work with ryegrass (Lolium perenne) is presented, exploring the impact of the physical presence of an LNAPL (mineral oil) on plant growth, root distribution and oil removal. The presence of the oil was found to significantly impact root biomass and distribution, leading to zones of increased root growth alongside decreased shoot growth. Significant removal of the LNAPL was noted in both hydroponic conditions and planted soil

Genetic determinants of HSP70 gene expression following heat shock

The regulation of heat shock protein expression is of significant physiological and pathophysiological significance. Here we show that genetic diversity is an important determinant of heat shock protein 70 expression involving local, likely cis-acting, polymorphisms. We define DNA sequence variation for the highly homologous HSPA1A and HSPA1B genes in the major histocompatibility complex on chromosome 6p21 and establish quantitative and specific assays for determining transcript abundance. We show for lymphoblastoid cell lines established from individuals of African ancestry that following heat shock, expression of HSPA1B is associated with rs400547 (P 3.88 × 10−8) and linked single nucleotide polymorphisms (SNPs) located 62–93 kb telomeric to HSPA1B. This association was found to explain 31 and 29% of the variance in HSPA1B expression following heat shock or in resting cells, respectively. The associated SNPs show marked variation in minor allele frequency among populations, being more common in individuals of African ancestry, and are located in a region showing population-specific haplotypic block structure. The work illustrates how analysis of a heritable induced expression phenotype can be highly informative in defining functionally important genetic variation

Architecture and roles of periplasmic adaptor proteins in tripartite efflux assemblies.

Recent years have seen major advances in the structural understanding of the different components of tripartite efflux assemblies, which encompass the multidrug efflux (MDR) pumps and type I secretion systems. The majority of these investigations have focused on the role played by the inner membrane transporters and the outer membrane factor (OMF), leaving the third component of the system - the Periplasmic Adaptor Proteins (PAPs) - relatively understudied. Here we review the current state of knowledge of these versatile proteins which, far from being passive linkers between the OMF and the transporter, emerge as active architects of tripartite assemblies, and play diverse roles in the transport process. Recognition between the PAPs and OMFs is essential for pump assembly and function, and targeting this interaction may provide a novel avenue for combating multidrug resistance. With the recent advances elucidating the drug efflux and energetics of the tripartite assemblies, the understanding of the interaction between the OMFs and PAPs is the last piece remaining in the complete structure of the tripartite pump assembly puzzle

What has GWAS done for HLA and disease associations?

The major histocompatibility complex (MHC) is located in chromosome 6p21 and contains crucial regulators of immune response, including human leucocyte antigen (HLA) genes, alongside other genes with nonimmunological roles. More recently, a repertoire of noncoding RNA genes, including expressed pseudogenes, has also been identified. The MHC is the most gene dense and most polymorphic part of the human genome. The region exhibits haplotype-specific linkage disequilibrium patterns, contains the strongest cis- and trans-eQTLs/meQTLs in the genome and is known as a hot spot for disease associations. Another layer of complexity is provided to the region by the extreme structural variation and copy number variations. While the HLA-B gene has the highest number of alleles, the HLA-DR/DQ subregion is structurally most variable and shows the highest number of disease associations. Reliance on a single reference sequence has complicated the design, execution and analysis of GWAS for the MHC region and not infrequently, the MHC region has even been excluded from the analysis of GWAS data. Here, we contrast features of the MHC region with the rest of the genome and highlight its complexities, including its functional polymorphisms beyond those determined by single nucleotide polymorphisms or single amino acid residues. One of the several issues with customary GWAS analysis is that it does not address this additional layer of polymorphisms unique to the MHC region. We highlight alternative approaches that may assist with the analysis of GWAS data from the MHC region and unravel associations with all functional polymorphisms beyond single SNPs. We suggest that despite already showing the highest number of disease associations, the true extent of the involvement of the MHC region in disease genetics may not have been uncovered