Gotowe bibliografie tematyczne / Crowded lipid membrane biophysics

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Gotowa bibliografia na temat „Crowded lipid membrane biophysics”

Autor: Grafiati
Data publikacji: 6 września 2023

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Artykuły w czasopismach na temat "Crowded lipid membrane biophysics"

1

Erwin, Nelli, Satyajit Patra, Mridula Dwivedi, Katrin Weise, and Roland Winter. "Influence of isoform-specific Ras lipidation motifs on protein partitioning and dynamics in model membrane systems of various complexity." Biological Chemistry 398, no. 5-6 (2017): 547–63. http://dx.doi.org/10.1515/hsz-2016-0289.

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Abstract The partitioning of the lipidated signaling proteins N-Ras and K-Ras4B into various membrane systems, ranging from single-component fluid bilayers, binary fluid mixtures, heterogeneous raft model membranes up to complex native-like lipid mixtures (GPMVs) in the absence and presence of integral membrane proteins have been explored in the last decade in a combined chemical-biological and biophysical approach. These studies have revealed pronounced isoform-specific differences regarding the lateral distribution in membranes and formation of protein-rich membrane domains. In this context, we will also discuss the effects of lipid head group structure and charge density on the partitioning behavior of the lipoproteins. Moreover, the dynamic properties of N-Ras and K-Ras4B have been studied in different model membrane systems and native-like crowded milieus. Addition of crowding agents such as Ficoll and its monomeric unit, sucrose, gradually favors clustering of Ras proteins in forming small oligomers in the bulk; only at very high crowder concentrations association is disfavored.
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2

Arnarez, C., S. J. Marrink, and X. Periole. "Molecular mechanism of cardiolipin-mediated assembly of respiratory chain supercomplexes." Chemical Science 7, no. 7 (2016): 4435–43. http://dx.doi.org/10.1039/c5sc04664e.

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We reveal the molecular mechanism by which cardiolipin glues respiratory complexes into supercomplexes. This mechanism defines a new biophysico-chemical pathway of protein–lipid interplay, with broad general implications for the dynamic organization of crowded cell membranes.
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Kessler, Michael S., and Susan Gillmor. "Lipid Membrane Phase Dynamics." Biophysical Journal 104, no. 2 (2013): 248a. http://dx.doi.org/10.1016/j.bpj.2012.11.1398.

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Nawrocki, Grzegorz, Wonpil Im, Yuji Sugita, and Michael Feig. "Clustering and dynamics of crowded proteins near membranes and their influence on membrane bending." Proceedings of the National Academy of Sciences 116, no. 49 (2019): 24562–67. http://dx.doi.org/10.1073/pnas.1910771116.

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Atomistic molecular dynamics simulations of concentrated protein solutions in the presence of a phospholipid bilayer are presented to gain insights into the dynamics and interactions at the cytosol–membrane interface. The main finding is that proteins that are not known to specifically interact with membranes are preferentially excluded from the membrane, leaving a depletion zone near the membrane surface. As a consequence, effective protein concentrations increase, leading to increased protein contacts and clustering, whereas protein diffusion becomes faster near the membrane for proteins that do occasionally enter the depletion zone. Since protein–membrane contacts are infrequent and short-lived in this study, the structure of the lipid bilayer remains largely unaffected by the crowded protein solution, but when proteins do contact lipid head groups, small but statistically significant local membrane curvature is induced, on average.
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Fischer, Wolfgang B. "Assembling Within The Lipid Membrane: Viral Membrane Proteins." Biophysical Journal 96, no. 3 (2009): 338a—339a. http://dx.doi.org/10.1016/j.bpj.2008.12.3823.

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Mitchison-Field, Lorna MY, and Brittany J. Belin. "Bacterial lipid biophysics and membrane organization." Current Opinion in Microbiology 74 (August 2023): 102315. http://dx.doi.org/10.1016/j.mib.2023.102315.

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7

Ho, Chian Sing, Nawal K. Khadka, Fengyu She, Jianfeng Cai, and Jianjun Pan. "Polyglutamine aggregates impair lipid membrane integrity and enhance lipid membrane rigidity." Biochimica et Biophysica Acta (BBA) - Biomembranes 1858, no. 4 (2016): 661–70. http://dx.doi.org/10.1016/j.bbamem.2016.01.016.

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Wang, Hongyin, Kandice R. Levental, Joseph H. Lorent, Adhvikaa A. Revathi, and Ilya Levental. "Lipid scrambling facilitates membrane vesiculation through decreasing membrane stiffness." Biophysical Journal 122, no. 3 (2023): 22a—23a. http://dx.doi.org/10.1016/j.bpj.2022.11.347.

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Hoopes, Matthew I., Roland Faller, and Marjorie L. Longo. "Membrane Curvature Modeling and Lipid Organization in Supported Lipid Bilayers." Biophysical Journal 98, no. 3 (2010): 78a—79a. http://dx.doi.org/10.1016/j.bpj.2009.12.445.

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Sodt, Alexander J., Olivier Soubias, Klaus Gawrisch, and Richard W. Pastor. "Lipid-Lipid Coupling to Membrane Curvature by Simulation and NMR." Biophysical Journal 110, no. 3 (2016): 243a. http://dx.doi.org/10.1016/j.bpj.2015.11.1340.

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