Results 101 to 110 of about 1,288,108 (273)

Ataxin-1 fusion partners alter polyQ lethality and aggregation [PDF]

open access: yes, 2007
Intranuclear inclusion bodies (IBs) are the histopathologic markers of multiple protein folding diseases. IB formation has been extensively studied using fluorescent fusion products of pathogenic polyglutamine (polyQ) expressing proteins.
Rich, T.   +5 more
core   +2 more sources

Structure‐forward targeting of claudins with synthetic binders

open access: yesFEBS Letters, EarlyView.
Claudins form the paracellular barriers between epithelial and endothelial tissues at tight junctions and are targets for molecular binders with the goal of modulating barrier permeability. Claudin‐binding molecules are relevant in drug delivery or in altering claudin interactions with disease‐causing proteins.
Alex J. Vecchio
wiley   +1 more source

Discerning protein pools by selective staining with self‐labeling tags

open access: yesFEBS Letters, EarlyView.
Cell surface proteins have an intra‐ and extracellular pool. Combining genetic fusion to self‐labeling tags that can be addressed with small molecule fluorophores allows separating these pools. We highlight recent developments and techniques for state‐of‐the‐art interrogation of cell surface proteins in the complex tissue setting.
Kati Fischermanns, Johannes Broichhagen
wiley   +1 more source

Aging differentially affects multiple aspects of vesicle fusion kinetics.

open access: yesPLoS ONE, 2011
How fusion pore formation during exocytosis affects the subsequent release of vesicle contents remains incompletely understood. It is unclear if the amount released per vesicle is dependent upon the nature of the developing fusion pore and whether full ...
Mark P Zanin   +3 more
doaj   +1 more source

Peripheral lysosomes recruit PLEKHG3 to focal adhesions and restrain protrusion dynamics

open access: yesFEBS Letters, EarlyView.
Proximity‐dependent labeling at the LAMTOR complex revealed the Rho GEF PLEKHG3 as a lysosome‐proximal protein directing the study toward the influence of lysosome positioning on actin dynamics and cell motility. We show that PLEKHG3 colocalizes with lysosomes at focal adhesion sites and observe that forced peripheral dispersion of lysosomes hinders ...
Rainer Ettelt   +8 more
wiley   +1 more source

Engineering peptides into antibodies—opportunities and strategies for therapeutic innovation

open access: yesFEBS Letters, EarlyView.
Peptides and antibodies occupy complementary therapeutic niches. Peptides recognize difficult targets in a compact format, while antibodies add specificity, long half‐life, and effector functions. This review examines strategies that merge both modalities—peptide grafting into loops, terminal and Fc fusions, and bioconjugation—highlighting how ...
Jinling Wang   +2 more
wiley   +1 more source

Gas hydrate growth and dissociation in narrow pore networks: capillary inhibition and hysteresis phenomena [PDF]

open access: yes, 2009
Marine sediments hosting gas hydrates are commonly fine-grained (silts, muds, clays) with very narrow mean pore diameters (0.1 mm). This has led to speculation that capillary phenomena could play an important role in controlling hydrate distribution in
Webber, J. Beau W.   +5 more
core   +1 more source

Fusion pore dynamics of large secretory vesicles define a distinct mechanism of exocytosis [PDF]

open access: yesJ Cell Biol, 2023
Biton T   +6 more
europepmc   +2 more sources

Synaptobrevin2 monomers and dimers differentially engage to regulate the functional trans-SNARE assembly

open access: yesLife Science Alliance
This work demonstrates different factors controlling the synaptobrevin2 dimer-to-monomer ratio, which has ramifications in fusion pore stability. The precise cell-to-cell communication relies on SNARE-catalyzed membrane fusion.
Swapnali S Patil   +6 more
doaj   +1 more source

Liver organoids: modelling complexity in homeostasis and disease

open access: yesFEBS Letters, EarlyView.
Studying liver in vitro has been challenging because simple 2D cell cultures fail to capture liver's cellular and architectural complexity. To bridge this gap, scientists increasingly use organoids, 3D liver models which better mimic liver composition and function. This review examines recent advances in liver organoid complexity and realism, discusses
Anna M. Dowbaj, Meritxell Huch
wiley   +1 more source

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