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      Sustained enzymatic activity and flow in crowded protein droplets

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          Abstract

          Living cells harvest energy from their environments to drive the chemical processes that enable life. We introduce a minimal system that operates at similar protein concentrations, metabolic densities, and length scales as living cells. This approach takes advantage of the tendency of phase-separated protein droplets to strongly partition enzymes, while presenting minimal barriers to transport of small molecules across their interface. By dispersing these microreactors in a reservoir of substrate-loaded buffer, we achieve steady states at metabolic densities that match those of the hungriest microorganisms. We further demonstrate the formation of steady pH gradients, capable of driving microscopic flows. Our approach enables the investigation of the function of diverse enzymes in environments that mimic cytoplasm, and provides a flexible platform for studying the collective behavior of matter driven far from equilibrium.

          Abstract

          Living cells can harvest environmental energy to drive chemical processes. Here the authors design a minimal artificial system that achieves steady states at similar metabolic densities to microorganisms.

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          Ror2 signaling regulates Golgi structure and transport through IFT20 for tumor invasiveness

          Signaling through the Ror2 receptor tyrosine kinase promotes invadopodia formation for tumor invasion. Here, we identify intraflagellar transport 20 (IFT20) as a new target of this signaling in tumors that lack primary cilia, and find that IFT20 mediates the ability of Ror2 signaling to induce the invasiveness of these tumors. We also find that IFT20 regulates the nucleation of Golgi-derived microtubules by affecting the GM130-AKAP450 complex, which promotes Golgi ribbon formation in achieving polarized secretion for cell migration and invasion. Furthermore, IFT20 promotes the efficiency of transport through the Golgi complex. These findings shed new insights into how Ror2 signaling promotes tumor invasiveness, and also advance the understanding of how Golgi structure and transport can be regulated.
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            Double-slit photoelectron interference in strong-field ionization of the neon dimer

            Wave-particle duality is an inherent peculiarity of the quantum world. The double-slit experiment has been frequently used for understanding different aspects of this fundamental concept. The occurrence of interference rests on the lack of which-way information and on the absence of decoherence mechanisms, which could scramble the wave fronts. Here, we report on the observation of two-center interference in the molecular-frame photoelectron momentum distribution upon ionization of the neon dimer by a strong laser field. Postselection of ions, which are measured in coincidence with electrons, allows choosing the symmetry of the residual ion, leading to observation of both, gerade and ungerade, types of interference.
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              Biomolecular condensates: organizers of cellular biochemistry

              In addition to membrane-bound organelles, eukaryotic cells feature various membraneless compartments, including the centrosome, the nucleolus and various granules. Many of these compartments form through liquid–liquid phase separation, and the principles, mechanisms and regulation of their assembly as well as their cellular functions are now beginning to emerge.
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                Author and article information

                Contributors
                eric.dufresne@mat.ethz.ch
                paola.laurino@oist.jp
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                1 November 2021
                1 November 2021
                2021
                : 12
                : 6293
                Affiliations
                [1 ]GRID grid.5801.c, ISNI 0000 0001 2156 2780, Department of Materials, , ETH Zürich, ; 8093 Zürich, Switzerland
                [2 ]GRID grid.250464.1, ISNI 0000 0000 9805 2626, Protein Engineering and Evolution Unit, , Okinawa Institute of Science and Technology Graduate University, ; 1919-1 Tancha, Onna, 904-0495 Okinawa Japan
                [3 ]GRID grid.419514.c, ISNI 0000 0004 0491 5187, Max Planck Institute for Dynamics and Self-Organization (MPIDS), ; D-37077 Göttingen, Germany
                [4 ]GRID grid.4991.5, ISNI 0000 0004 1936 8948, Rudolf Peierls Centre for Theoretical Physics, , University of Oxford, ; Oxford, OX1 3PU United Kingdom
                Author information
                http://orcid.org/0000-0002-4376-2510
                http://orcid.org/0000-0001-5305-7658
                http://orcid.org/0000-0002-3149-4002
                http://orcid.org/0000-0002-3725-2645
                Article
                26532
                10.1038/s41467-021-26532-0
                8560906
                34725341
                e428084f-9a07-48e4-9444-a3908da370d9
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 10 June 2021
                : 11 October 2021
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100004199, Okinawa Institute of Science and Technology Graduate University (Okinawa Institute of Science and Technology);
                Categories
                Article
                Custom metadata
                © The Author(s) 2021

                Uncategorized
                biophysical chemistry,enzymes,molecular biophysics,physical chemistry
                Uncategorized
                biophysical chemistry, enzymes, molecular biophysics, physical chemistry

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