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Biology subjects

Connell, S. D. A.

Publications and source records attributed to Connell, S. D. A..

2 recordsLinked to original sources

Fibrinogen αC-subregions critically contribute blood clot fibre growth, mechanical stability and resistance to fibrinolysis

Fibrinogen is essential for blood coagulation. The C-terminus of the fibrinogen -chain (C-region) is composed of an C-domain and C-connector. Two recombinant fibrinogen variants (390 and 220) were produced to investigate the role of subregions in modulating clot stability and resistance to lysis. The 390 variant, truncated before the C-domain, produced clots with a denser structure and thinner fibres. In contrast, the 220 variant, truncated at the start of the C-connector, produced clots that were porous with short stunted fibres and visible fibre ends. These clots were mechanically weak and susceptible to lysis. Our data demonstrate differential effects for the C-subregions in fibrin polymerisation, clot mechanical strength, and fibrinolytic susceptibility. Furthermore, we demonstrate that the C-subregions are key for promoting longitudinal fibre growth. Together, these findings highlight critical functions of the C-subregions in relation to clot structure and stability, with future implications for development of novel therapeutics for thrombosis.

physiology↗

Proteoliposomes as energy transferring nanomaterials: enhancing the spectral range of light-harvesting proteins using lipid-linked chromophores

Biology provides a suite of optically-active nanomaterials in the form of \"light harvesting\" protein-chlorophyll complexes, however, these have drawbacks including their limited spectral range. We report the generation of model lipid membranes (proteoliposomes) incorporating the photosynthetic protein Light-Harvesting Complex II (LHCII) and lipid-tethered Texas Red (TR) chromophores that act as a \"bio-hybrid\" energy transferring nanomaterial. The effective spectral range of the protein is enhanced due to highly efficient energy transfer from the TR chromophores (up to 94%), producing a marked increase in LHCII fluorescence (up to 3x). Our self-assembly procedure offers excellent modularity allowing the incorporation of a range of concentrations of energy donors (TR) and acceptors (LHCII), allowing the energy transfer efficiency (ETE) and LHCII fluorescence to be tuned as desired. Fluorescence Lifetime Imaging Microscopy (FLIM) provides single-proteoliposome-level quantification of ETE, revealing distributions within the population and proving that functionality is maintained on a surface. Our membrane-based system acts as a controllable light harvesting nanomaterial with potential applications as thin films in photo-active devices.\n\n\n\nO_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=92 SRC=\"FIGDIR/small/609255v1_ufig1.gif\" ALT=\"Figure 1\">\nView larger version (32K):\norg.highwire.dtl.DTLVardef@e663f3org.highwire.dtl.DTLVardef@1abfa78org.highwire.dtl.DTLVardef@1c90d5aorg.highwire.dtl.DTLVardef@8b99db_HPS_FORMAT_FIGEXP M_FIG Table of Contents Figure C_FIG

biophysics↗