Nuclear Pore Complexes (NPCs) are key cellular transporter that control nucleocytoplasmic transport in eukaryotic cells, but its transport mechanism is still not understood. The centerpiece of NPC transport is the assembly of intrinsically disordered polypeptides, known as FG nucleoporins, lining its passageway. Their conformations and collective dynamics during transport are difficult to assess in vivo. In vitro investigations provide partially conflicting results, lending support to different models of transport, which invoke various conformational transitions of the FG nucleoporins induced by the cargo-carrying transport proteins. We show that the spatial organization of FG nucleoporin assemblies with the transport proteins can be understood within a first principles biophysical model with a minimal number of key physical variables, such as the average protein interaction strengths and spatial densities. These results address some of the outstanding controversies and suggest how molecularly divergent NPCs in different species can perform essentially the same function.
[1] Applying a simple general procedure for identifying aftershocks, we investigate their statistical properties for a high-resolution earthquake catalog covering Southern California. We compare our results with those obtained by using other methods in order to show which features truly characterize aftershock sequences and which depend on the definition of aftershocks. Features robust across methods include the p value in the Omori-Utsu law for large main shocks, Båth's law, and the productivity law with an exponent smaller than the b value in the Gutenberg-Richter law. The identification of a typical aftershock distance with the rupture length is a feature we confirm as well as a power law decay in the spatial distribution of aftershocks with an exponent less than 2. Other results we obtain, but not common to all other works including Marsan and Lengliné (2008), Zhuang et al. (2008), are (a) p values that do not increase with the main shock magnitude; (b) the duration of bare aftershock sequences that scales with the main shock magnitude; (c) an additional power law in the temporal variation, at intermediate times, in the rate of aftershocks for main shocks of small and intermediate magnitude; and (d) a b value for the Gutenberg-Richter law of background events that is sensibly larger than that of aftershocks. Tests on synthetic catalogs generated by the epidemic-type aftershock sequence model corroborate the validity of our approach.
We demonstrate for the first time that spiral wave chimeras-spiral waves with spatially extended unsynchronzied cores-can exist in complex oscillatory and even locally chaotic homogeneous systems under nonlocal coupling. Using ideas from phase synchronization, we show in particular that the unsynchronized cores exhibit a distribution of different frequencies, thus generalizing the main concept of chimera states beyond simple oscillatory systems. In contrast to simple oscillatory systems, we find that spiral wave chimeras in complex oscillatory and locally chaotic systems are characterized by the presence of synchronization defect lines (SDLs), along which the dynamics follows a periodic behavior different from that of the bulk. Whereas this is similar to the case of local coupling, the type of the prevailing SDLs is very different.
Characterization of the interactions between nanosize ligands and polymeric substrates is important for predictive design of nanomaterials and in biophysical applications. The multivalent nature of the polymer-nanoparticle interaction and the dynamics of multiple internal conformations of the polymer chains makes it difficult to infer microscopic interactions from macroscopic binding assays. Using coarse-grained simulations, we estimate the free energy of binding between a nanoparticle and a surface-grafted polymeric substrate as a function of pertinent parameters such as polymer chain length, nanoparticle size, and microscopic polymer-nanoparticle attraction. We also investigate how the presence of the nanoparticle affects the internal configurations of the polymeric substrate, and estimate the entropic cost of binding. The results have important implications for the understanding of complex macromolecular assemblies.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.