182 research outputs found
Dynamic buckling of actin within filopodia
Filopodia are active tubular structuresprotruding from the cell surface which allow the cell to sense and interact with the surrounding environment through repetitive elongation-retraction cycles. The mechanical behavior of filo-podia has been studied by measuring the traction forces exerted on external sub-strates.1 These studies have revealed that internal actin flow can transduce a force across the cell surface through transmem-brane linkers like integrins. In addition to the elongation-retraction behavior filo-podia also exhibit a buckling and rota-tional behavior. Filopodial buckling in conjunction with rotation enables th
EagrĂĄn de na scĂ©alta idirnĂĄisiĂșnta Ăł na Cruacha Gorma a bhailigh SeĂĄn Ă hEochaidh do ChoimisiĂșn BĂ©aloideasa Ăireann i 1947 agus 1948
Sa saothar seo, cuirtear in eagar trĂocha scĂ©al idirnĂĄisiĂșnta a bailĂodh sna Cruacha
Gorma i dTĂr Chonaill sna blianta 1947 agus 1948. Is iad na haidhmeanna atĂĄ ag an
saothar:
1. Eagrån de na scéalta seo a chur ar fåil don chéad uair, scéalta når cuireadh in
eagar cheana.
2. Gaeilge na scĂ©alta a chaighdeĂĄnĂș de rĂ©ir FoclĂłir Gaeilge-BĂ©arla, (Ă DĂłnaill,
1977) agus Gramadach na Gaeilge agus LitriĂș na Gaeilge, An CaighdeĂĄn OifigiĂșil,
(2004), ach amhĂĄin nuair a bhĂonn coimhlint idir an CaighdeĂĄn agus canĂșint na
scĂ©alaithe mar a scrĂobhadh sĂos Ă ag an bhailitheoir, SeĂĄn Ă hEochaidh. Nuair a bhĂonn
coimhlint idir an CaighdeĂĄn agus an chanĂșint, taobhaĂtear leis an chanĂșint sa saothar.
3. An méid staidéir atå déanta cheana ar bhéaloideas na gCruach, agus ar an ról
Ă©achtach a bhĂ ag Ă hEochaidh ina chaomhnĂș a mhĂ©adĂș.
Bhailigh SeĂĄn Ă hEochaidh na scĂ©alta seo do ChomisiĂșin BĂ©aloideasa Ăireann, agus tĂĄ
lĂĄmhscrĂbhinnĂ an bhailitheora caomhnaithe mar chuid de Chnuasach BhĂ©aloideas
Ăireann (CBĂ) sa CholĂĄiste Ollscoile, Baile Ătha Cliath. Is iad na lĂĄmhscrĂbhinnĂ seo, a
bhfuil fĂĄil orthu chomh maith i bhfoirm mhicreascannĂĄn i leabharlann Ollscoil na
hĂireann, MĂĄ Nuad, a ĂșsĂĄidtear mar bhunĂĄbhar sa saothar.
I gCaibidil 1, tugtar an modh eagarthóireachta a chuirtear i bhfeidhm ar théacsanna na
scéalta, na hathruithe i dtreo an Chaighdeåin a dhéantar, agus na hathruithe nach
gcuirtear i bhfeidhm nuair a dhĂ©antar iarracht tĂșs ĂĄite a thabhairt do chanĂșint na
scéalaithe.
I gCaibidil 2, déantar plé ar cheithre åbhar inspéise de Ghaeilge na gCruach a thåinig
chun cinn nuair a bhà na scéalta å gcur in eagar.
I gCaibidil 3, tugtar trĂocha scĂ©al idirnĂĄisiĂșnta agus iad curtha in eagar. Chomh maith
leis an phlé a dhéantar ar Ghaeilge na scéalta, mar a luadh thuas, cuirtear athruithe i
bhfeidhm i bponcaĂocht agus i leagan amach thĂ©acs na scĂ©alta.
I gCaibidil 4 dĂ©antar plĂ© ar scĂ©al amhĂĄin sa chnuasach, scĂ©al an Fhir MhĂłir. BailĂodh
dhĂĄ leagan den scĂ©al seo Ăłn scĂ©alaĂ, Anna Nic an Luain, Cruach Thoibrid, agus faightear
idir chosĂșlachtaĂ agus Ă©agsĂșlachtaĂ sna leaganacha seo. DĂ©antar comparĂĄid idir an dĂĄ
leagan sin, chomh maith le plĂ© a dhĂ©anamh ar an scĂ©al mar a bailĂodh Ă© sna Cruacha
agus i gceantracha eile i dTir Chonaill.
Sa chĂ©ad aguisĂn a thĂ©ann leis an saothar seo, tugtar eolas ar na scĂ©alta a fhaightear ann.
Tugtar ainmneacha na scéalta, uimhreacha na scéalta de réir chlår
Aarne/Thompson/Uther (ATU), agus cur sĂos ar na scĂ©alta idirnĂĄisiĂșnta a fhaightear
iontu, ainmneacha na scéalaithe agus cad as a bhfuair siad a gcuid scéalta, må tå an teolas
sin ar fĂĄil sna lĂĄmhscrĂbhinnĂ. Sa dara aguisĂn, tugtar leagan na lĂĄmhscrĂbhinnĂ
den scĂ©al An luchĂłg Ăœ an bheacĂłg, dĂreach mar a scrĂobh SeĂĄn Ă hEochaidh sĂos Ă© Ăłn
scĂ©alaĂ Anna Nic an Luain. Sa trĂĂș aguisĂn, tugtar liosta iomlĂĄn de na scĂ©alta
idirnĂĄisiĂșnta a bailĂodh sna Cruacha Gorma i 1947 agus 1948
Continuous cocrystallization of benzoic acid and isonicotinamide by mixing-induced supersaturation : exploring opportunities between reactive and antisolvent crystallization concepts
This study combines reactive and antisolvent crystallization concepts via mixing-induced supersaturation to demonstrate a wider range of options for solvent system selection in multicomponent crystallization. This approach was applied to investigate continuous crystallization of 1:1 and 2:1 cocrystals of benzoic acid and isonicotinamide. Design of Experiments was used to identify conditions where pure cocrystal phases are obtained and a continuous mixing-induced cocrystallization process was implemented to selectively produce either 1:1 or 2:1 cocrystals
Dynamics of membrane nanotubes coated with I-BAR
Membrane deformation is a necessary step in a number of cellular processes such as filopodia and invadopodia formation and has been shown to involve membrane shaping proteins containing membrane binding domains from the IRSp53-MIM protein family. In reconstituted membranes the membrane shaping domains can efficiently deform negatively charged membranes into tubules without any other proteins present. Here, we show that the IM domain (also called I-BAR domain) from the protein ABBA, forms semi-flexible nanotubes protruding into Giant Unilamellar lipid Vesicles (GUVs). By simultaneous quantification of tube intensity and tubular shape we find both the diameter and stiffness of the nanotubes. I-BAR decorated tubes were quantified to have a diameter of ~50ânm and exhibit no stiffening relative to protein free tubes of the same diameter. At high protein density the tubes are immobile whereas at lower density the tubes diffuse freely on the surface of the GUV. Bleaching experiments of the fluorescently tagged I-BAR confirmed that the mobility of the tubes correlates with the mobility of the I-BAR on the GUV membrane. Finally, at low density of I-BAR the protein upconcentrates within tubes protruding into the GUVs. This implies that I-BAR exhibits strong preference for negatively curved membranes
Single Particle and PET-based Platform for Identifying Optimal Plasmonic Nano-Heaters for Photothermal Cancer Therapy
Plasmonic nanoparticle-based photothermal cancer therapy is a promising new tool to inflict localized and irreversible damage to tumor tissue by hyperthermia, without harming surrounding healthy tissue. We developed a single particle and positron emission tomography (PET)-based platform to quantitatively correlate the heat generation of plasmonic nanoparticles with their potential as cancer killing agents. In vitro, the heat generation and absorption cross-section of single irradiated nanoparticles were quantified using a temperature sensitive lipid-based assay and compared to their theoretically predicted photo-absorption. In vivo, the heat generation of irradiated nanoparticles was evaluated in human tumor xenografts in mice using 2-deoxy-2-[F-18]fluoro-D-glucose ((18)F-FDG) PET imaging. To validate the use of this platform, we quantified the photothermal efficiency of near infrared resonant silica-gold nanoshells (AuNSs) and benchmarked this against the heating of colloidal spherical, solid gold nanoparticles (AuNPs). As expected, both in vitro and in vivo the heat generation of the resonant AuNSs performed superior compared to the non-resonant AuNPs. Furthermore, the results showed that PET imaging could be reliably used to monitor early treatment response of photothermal treatment. This multidisciplinary approach provides a much needed platform to benchmark the emerging plethora of novel plasmonic nanoparticles for their potential for photothermal cancer therapy
FBAR syndapin 1 recognizes and stabilizes highly curved tubular membranes in a concentration dependent manner
Syndapin 1 FBAR, a member of the Bin-amphiphysin-Rvs (BAR) domain protein family, is known to induce membrane curvature and is an essential component in biological processes like endocytosis and formation and growth of neurites. We quantify the curvature sensing of FBAR on reconstituted porcine brain lipid vesicles and show that it senses membrane curvature at low density whereas it induces and reinforces tube stiffness at higher density. FBAR strongly up-concentrates on the high curvature tubes pulled out of Giant Unilamellar lipid Vesicles (GUVs), this sorting behavior is strongly amplified at low protein densities. Interestingly, FBAR from syndapin 1 has a large affinity for tubular membranes with curvatures larger than its own intrinsic concave curvature. Finally, we studied the effect of FBAR on membrane relaxation kinetics with high temporal resolution and found that the protein increases relaxation time of the tube holding force in a density-dependent fashion
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