667 research outputs found

    Fluorine substitutions in an antigenic peptide selectively modulate T cell receptor binding in a minimally perturbing manner

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    T cell receptor (TCR) recognition of antigenic peptides bound and presented by major histocompatibility complex (MHC) molecules forms the basis of the cellular immune response to pathogens and cancer. TCRs bind peptide/MHC molecules weakly and with fast kinetics, features which have hindered detailed biophysical studies of these interactions. Modified peptides resulting in enhanced TCR binding could help overcome these challenges. Further, there is considerable interest in using modified peptides with enhanced TCR binding as the basis for clinical vaccines. Here, we studied how fluorine substitutions in an antigenic peptide can selectively impact TCR recognition. Using a structure-guided design approach, we found that fluorination of the HTLV-1 Tax11-19 peptide (Tax) enhanced binding by the Tax-specific TCR A6, yet weakened binding by the Tax-specific TCR B7. The changes in affinity were consistent with crystallographic structures and fluorine chemistry, and with A6, independent of other substitutions in the interface. Peptide fluorination thus provides a means to selectively modulate TCR binding affinity without significantly perturbing peptide composition or structure. Lastly, in probing the mechanism of fluorine’s effect on TCR binding, our data were most consistent with fluorine’s unique “polar hydrophobicity,” a finding which should impact other attempts to alter molecular recognition with fluorine

    Simultaneous non-negative matrix factorization for multiple large scale gene expression datasets in toxicology

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    Non-negative matrix factorization is a useful tool for reducing the dimension of large datasets. This work considers simultaneous non-negative matrix factorization of multiple sources of data. In particular, we perform the first study that involves more than two datasets. We discuss the algorithmic issues required to convert the approach into a practical computational tool and apply the technique to new gene expression data quantifying the molecular changes in four tissue types due to different dosages of an experimental panPPAR agonist in mouse. This study is of interest in toxicology because, whilst PPARs form potential therapeutic targets for diabetes, it is known that they can induce serious side-effects. Our results show that the practical simultaneous non-negative matrix factorization developed here can add value to the data analysis. In particular, we find that factorizing the data as a single object allows us to distinguish between the four tissue types, but does not correctly reproduce the known dosage level groups. Applying our new approach, which treats the four tissue types as providing distinct, but related, datasets, we find that the dosage level groups are respected. The new algorithm then provides separate gene list orderings that can be studied for each tissue type, and compared with the ordering arising from the single factorization. We find that many of our conclusions can be corroborated with known biological behaviour, and others offer new insights into the toxicological effects. Overall, the algorithm shows promise for early detection of toxicity in the drug discovery process

    The aesthetic and cultural pursuits of patients with stroke

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    peer-reviewedTables to accompany this article on second fileGOAL: There has been an increasing interest in the arts in healthcare, with a suggestion that the arts and aesthetics can augment patient outcomes in stroke and other illnesses. Designing such programmes requires better knowledge of the artistic, aesthetic and cultural pursuits of people affected by stroke. The aim of this study was to obtain the insights of this group about the profile of arts and aesthetics activities in their lives as well as the influence of stroke on these aspects. MATERIALS AND METHODS: Patients attending a stroke service were administered questions adapted from the Irish Arts Council’s 2006 questionnaire on participation in aesthetics and cultural pursuits, Information was also collected on stroke type and present functional and cognitive status. Thirty-eight patients were interviewed. Of these, twenty were inpatients in hospital at the time of the interview and eighteen were interviewed in an outpatient setting. FINDINGS: Popular activities included mainstream cinema, listening to music, dancing, attending plays or musicals and being outdoors. Many patients ceased these activities after their stroke, mostly due to health issues and inaccessibility. The majority of patients valued the importance of the arts in the healthcare setting. CONCLUSION: This study gives a perspective for the first time on the aesthetic and cultural pursuits of stroke patients prior to their stroke. It portrays a wide variety of cultural and leisure activities, and the cessation of these post-stroke. It revealed the restrictions patients felt on gaining access to leisure pursuits both while in hospital and following discharge.Acceptedpeer-reviewe

    Interspecific Variation in One-Carbon Metabolism within the Ovarian Follicle, Oocyte, and Preimplantation Embryo: Consequences for Epigenetic Programming of DNA Methylation

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    One-carbon (1C) metabolism provides methyl groups for the synthesis and/or methylation 20 of purines and pyrimidines, biogenic amines, proteins and phospholipids. Our understanding of 21 how 1C pathways operate, however, pertains mostly to the (rat) liver. Here we report that 22 transcripts for all bar two genes (i.e. BHMT, MAT1A) encoding enzymes in the linked methionine-23 folate cycles are expressed in all cell types within the ovarian follicle, oocyte and blastocyst in the 24 cow, sheep and pig; as well as in rat granulosa cells (GCs) and human KGN cells. BHMT protein 25 was absent in bovine theca and GCs, as was activity of this enzyme in GCs. Mathematical modelling 26 predicted that absence of this enzyme would lead to more volatile S-adenosylmethionine-mediated 27 transmethylation in response to 1C substrate (e.g., methionine) or cofactor provision. We tested the 28 sensitivity of bovine GCs to reduced methionine (from 50 to 10 ”M) and observed a diminished flux 29 of 1C units through the methionine cycle. We then used Reduced-Representation Bisulfite 30 Sequencing to demonstrate that this reduction in methionine during bovine embryo culture leads 31 to genome-wide alterations to DNA methylation in >1,600 genes, including a cohort of imprinted 32 genes linked to an abnormal fetal-overgrowth phenotype. Bovine ovarian and embryonic cells are 33 acutely sensitive to methionine, but further experimentation is required to determine the 34 significance of interspecific variation in BHMT expression. 3

    Franchises lost and gained: post-coloniality and the development of women’s rights in Canada

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    The Canadian constitution is to some extent characterised by its focus on equality, and in particular gender equality. This development of women’s rights in Canada and the greater engagement of women as political actors is often presented as a steady linear process, moving forwards from post-enlightenment modernity. This article seeks to disturb this ‘discourse of the continuous,’ by using an analysis of the pre-confederation history of suffrage in Canada to both refute a simplistic linear view of women’s rights development and to argue for recognition of the Indigenous contribution to the history of women’s rights in Canada. The gain of franchise and suffrage movements in Canada in the late nineteenth and early twentieth century are, rightly, the focus of considerable study (Pauker 2015), This article takes an alternative perspective. Instead, it examines the exercise of earlier franchises in pre-confederation Canada. In particular it analyses why franchise was exercised more widely in Lower Canada and relates this to the context of the removal of franchises from women prior to confederation

    The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

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    Abstract: Breast cancer is a common disease partially caused by genetic risk factors. Germline pathogenic variants in DNA repair genes BRCA1, BRCA2, PALB2, ATM, and CHEK2 are associated with breast cancer risk. FANCM, which encodes for a DNA translocase, has been proposed as a breast cancer predisposition gene, with greater effects for the ER-negative and triple-negative breast cancer (TNBC) subtypes. We tested the three recurrent protein-truncating variants FANCM:p.Arg658*, p.Gln1701*, and p.Arg1931* for association with breast cancer risk in 67,112 cases, 53,766 controls, and 26,662 carriers of pathogenic variants of BRCA1 or BRCA2. These three variants were also studied functionally by measuring survival and chromosome fragility in FANCM−/− patient-derived immortalized fibroblasts treated with diepoxybutane or olaparib. We observed that FANCM:p.Arg658* was associated with increased risk of ER-negative disease and TNBC (OR = 2.44, P = 0.034 and OR = 3.79; P = 0.009, respectively). In a country-restricted analysis, we confirmed the associations detected for FANCM:p.Arg658* and found that also FANCM:p.Arg1931* was associated with ER-negative breast cancer risk (OR = 1.96; P = 0.006). The functional results indicated that all three variants were deleterious affecting cell survival and chromosome stability with FANCM:p.Arg658* causing more severe phenotypes. In conclusion, we confirmed that the two rare FANCM deleterious variants p.Arg658* and p.Arg1931* are risk factors for ER-negative and TNBC subtypes. Overall our data suggest that the effect of truncating variants on breast cancer risk may depend on their position in the gene. Cell sensitivity to olaparib exposure, identifies a possible therapeutic option to treat FANCM-associated tumors
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