On the public citation graph

Endocytic proteins with prion-like domains form viscoelastic condensates that enable membrane remodeling

0 signed · 222 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1873-3468.13192openalex-snapshot

Molecular mechanisms of force production in clathrin‐mediated endocytosis

inferredcites →https://doi.org/10.1002/yea.1130openalex-snapshot

Optimized cassettes for fluorescent protein tagging in Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1007/978-1-4939-6421-5_21openalex-snapshot

Measuring Molecular Forces Using Calibrated Optical Tweezers in Living Cells

inferredcites →https://doi.org/10.1007/s00253-013-5386-8openalex-snapshot

Osmoporation: a simple way to internalize hydrophilic molecules into yeast

inferredcites →https://doi.org/10.1007/s11043-016-9308-xopenalex-snapshot

Modelling of the collision of two viscoelastic spherical shells

inferredcites →https://doi.org/10.1007/s40544-017-0177-3openalex-snapshot

Strength of adhesive contacts: Influence of contact geometry and material gradients

inferredcites →https://doi.org/10.1016/0021-9797(75)90018-1openalex-snapshot

Effect of contact deformations on the adhesion of particles

inferredcites →https://doi.org/10.1016/j.bbapap.2013.01.003openalex-snapshot

Protein disorder, prion propensities, and self-organizing macromolecular collectives

inferredcites →https://doi.org/10.1016/j.bpj.2013.08.037openalex-snapshot

The Role of Vimentin Intermediate Filaments in Cortical and Cytoplasmic Mechanics

inferredcites →https://doi.org/10.1016/j.bpj.2014.02.035openalex-snapshot

Force Generation by Endocytic Actin Patches in Budding Yeast

inferredcites →https://doi.org/10.1016/j.bpj.2016.10.040openalex-snapshot

Local Turgor Pressure Reduction via Channel Clustering

inferredcites →https://doi.org/10.1016/j.bpj.2017.09.029openalex-snapshot

Hallmarks of Reversible Separation of Living, Unperturbed Cell Membranes into Two Liquid Phases

inferredcites →https://doi.org/10.1016/j.ceb.2010.05.002openalex-snapshot

Interplay of proteins and lipids in generating membrane curvature

inferredcites →https://doi.org/10.1016/j.cell.2005.09.024openalex-snapshot

A Modular Design for the Clathrin- and Actin-Mediated Endocytosis Machinery

inferredcites →https://doi.org/10.1016/j.cell.2009.02.044openalex-snapshot

A Systematic Survey Identifies Prions and Illuminates Sequence Features of Prionogenic Proteins

inferredcites →https://doi.org/10.1016/j.cell.2012.01.047openalex-snapshot

Membrane Fission Is Promoted by Insertion of Amphipathic Helices and Is Restricted by Crescent BAR Domains

inferredcites →https://doi.org/10.1016/j.cell.2012.05.046openalex-snapshot

Plasma Membrane Reshaping during Endocytosis Is Revealed by Time-Resolved Electron Tomography

inferredcites →https://doi.org/10.1016/j.cell.2014.06.051openalex-snapshot

Probing the Stochastic, Motor-Driven Properties of the Cytoplasm Using Force Spectrum Microscopy

inferredcites →https://doi.org/10.1016/j.cell.2015.07.047openalex-snapshot

A Liquid-to-Solid Phase Transition of the ALS Protein FUS Accelerated by Disease Mutation

inferredcites →https://doi.org/10.1016/j.cell.2016.05.026openalex-snapshot

Mechanisms and Consequences of Macromolecular Phase Separation

inferredcites →https://doi.org/10.1016/j.cell.2016.06.051openalex-snapshot

Amyloid-like Self-Assembly of a Cellular Compartment

inferredcites →https://doi.org/10.1016/j.cell.2016.11.054openalex-snapshot

Spatiotemporal Control of Intracellular Phase Transitions Using Light-Activated optoDroplets

inferredcites →https://doi.org/10.1016/j.cell.2018.06.006openalex-snapshot

A Molecular Grammar Governing the Driving Forces for Phase Separation of Prion-like RNA Binding Proteins

inferredcites →https://doi.org/10.1016/j.cell.2018.06.032openalex-snapshot

Systematic Nanoscale Analysis of Endocytosis Links Efficient Vesicle Formation to Patterned Actin Nucleation

inferredcites →https://doi.org/10.1016/j.cell.2018.09.050openalex-snapshot

Changes of Cell Biochemical States Are Revealed in Protein Homomeric Complex Dynamics

inferredcites →https://doi.org/10.1016/j.cell.2020.03.046openalex-snapshot

G3BP1 Is a Tunable Switch that Triggers Phase Separation to Assemble Stress Granules

inferredcites →https://doi.org/10.1016/j.cell.2020.03.050openalex-snapshot

Competing Protein-RNA Interaction Networks Control Multiphase Intracellular Organization

inferredcites →https://doi.org/10.1016/j.celrep.2017.08.013openalex-snapshot

Spatiotemporal Control of Lipid Conversion, Actin-Based Mechanical Forces, and Curvature Sensors during Clathrin/AP-1-Coated Vesicle Biogenesis

inferredcites →https://doi.org/10.1016/j.ijsolstr.2006.11.002openalex-snapshot

A theory of amorphous viscoelastic solids undergoing finite deformations with application to hydrogels

inferredcites →https://doi.org/10.1016/j.jbiomech.2013.05.001openalex-snapshot

Determination of local and global elastic moduli of valve interstitial cells cultured on soft substrates

inferredcites →https://doi.org/10.1016/j.jmb.2018.06.023openalex-snapshot

Mechanics, Structure and Function of Biopolymer Condensates

inferredcites →https://doi.org/10.1016/j.jmb.2018.06.031openalex-snapshot

Advances in Understanding Stimulus-Responsive Phase Behavior of Intrinsically Disordered Protein Polymers

inferredcites →https://doi.org/10.1016/j.jmb.2018.06.038openalex-snapshot

A User’s Guide for Phase Separation Assays with Purified Proteins

inferredcites →https://doi.org/10.1016/j.molcel.2011.05.013openalex-snapshot

Opposing Effects of Glutamine and Asparagine Govern Prion Formation by Intrinsically Disordered Proteins

inferredcites →https://doi.org/10.1016/j.molcel.2019.06.044openalex-snapshot

Nucleo-cytoplasmic Partitioning of ARF Proteins Controls Auxin Responses in Arabidopsis thaliana

inferredcites →https://doi.org/10.1016/j.molcel.2020.10.030openalex-snapshot

A Selective Autophagy Pathway for Phase-Separated Endocytic Protein Deposits

inferredcites →https://doi.org/10.1016/j.sbi.2015.03.008openalex-snapshot

Relating sequence encoded information to form and function of intrinsically disordered proteins

inferredcites →https://doi.org/10.1016/j.sbi.2018.10.003openalex-snapshot

Conformational preferences and phase behavior of intrinsically disordered low complexity sequences: insights from multiscale simulations

inferredcites →https://doi.org/10.1021/la800956jopenalex-snapshot

Protein Diffusion Across the Interface in Aqueous Two-Phase Systems

inferredcites →https://doi.org/10.1038/nature01020openalex-snapshot

Curvature of clathrin-coated pits driven by epsin

inferredcites →https://doi.org/10.1038/nature02026openalex-snapshot

Global analysis of protein localization in budding yeast

inferredcites →https://doi.org/10.1038/ncb1918openalex-snapshot

Differential requirements for actin during yeast and mammalian endocytosis

inferredcites →https://doi.org/10.1038/ncb2307openalex-snapshot

Actin dynamics counteract membrane tension during clathrin-mediated endocytosis

inferredcites →https://doi.org/10.1038/nchem.2803openalex-snapshot

Phase behaviour of disordered proteins underlying low density and high permeability of liquid organelles

inferredcites →https://doi.org/10.1038/ncomms8875openalex-snapshot

Intrinsically disordered proteins drive membrane curvature

inferredcites →https://doi.org/10.1038/nmeth.1991openalex-snapshot

A simple, versatile method for GFP-based super-resolution microscopy via nanobodies

inferredcites →https://doi.org/10.1038/nrm.2017.132openalex-snapshot

Mechanisms of clathrin-mediated endocytosis

inferredcites →https://doi.org/10.1038/nrm.2017.7openalex-snapshot

Biomolecular condensates: organizers of cellular biochemistry

inferredcites →https://doi.org/10.1038/s41467-019-10554-wopenalex-snapshot

The prion-like domain of Drosophila Imp promotes axonal transport of RNP granules in vivo

inferredcites →https://doi.org/10.1038/s41557-021-00840-wopenalex-snapshot

Deciphering how naturally occurring sequence features impact the phase behaviours of disordered prion-like domains

inferredcites →https://doi.org/10.1039/c2sm26108aopenalex-snapshot

Measuring the elastic modulus of microgels using microdrops

inferredcites →https://doi.org/10.1063/1.3280222openalex-snapshot

Active-passive calibration of optical tweezers in viscoelastic media

inferredcites →https://doi.org/10.1073/pnas.1015892108openalex-snapshot

Membrane nanotubes induced by aqueous phase separation and stabilized by spontaneous curvature

inferredcites →https://doi.org/10.1073/pnas.1017150108openalex-snapshot

Active liquid-like behavior of nucleoli determines their size and shape in Xenopus laevis oocytes

inferredcites →https://doi.org/10.1073/pnas.1202789109openalex-snapshot

Ultrastructural dynamics of proteins involved in endocytic budding

inferredcites →https://doi.org/10.1073/pnas.1215462109openalex-snapshot

Force measurements on cargoes in living cells reveal collective dynamics of microtubule motors

inferredcites →https://doi.org/10.1073/pnas.1504822112openalex-snapshot

The disordered P granule protein LAF-1 drives phase separation into droplets with tunable viscosity and dynamics

inferredcites →https://doi.org/10.1073/pnas.1616199114openalex-snapshot

Membrane fission by protein crowding

inferredcites →https://doi.org/10.1073/pnas.1701877114openalex-snapshot

Direct observation of structure and dynamics during phase separation of an elastomeric protein

inferredcites →https://doi.org/10.1073/pnas.2017435118openalex-snapshot

Membrane bending by protein phase separation

inferredcites →https://doi.org/10.1083/jcb.201010104openalex-snapshot

P granules extend the nuclear pore complex environment in the C. elegans germ line

inferredcites →https://doi.org/10.1089/ten.tec.2018.0372openalex-snapshot

Mechanical Characterization by Mesoscale Indentation: Advantages and Pitfalls for Tissue and Scaffolds

inferredcites →https://doi.org/10.1091/mbc.e10-03-0181openalex-snapshot

Dissecting BAR Domain Function in the Yeast Amphiphysins Rvs161 and Rvs167 during Endocytosis

inferredcites →https://doi.org/10.1091/mbc.e13-10-0618openalex-snapshot

Role of turgor pressure in endocytosis in fission yeast

inferredcites →https://doi.org/10.1091/mbc.e19-09-0504openalex-snapshot

Dynamic actin cross-linking governs the cytoplasm’s transition to fluid-like behavior

inferredcites →https://doi.org/10.1103/physrevresearch.2.033222openalex-snapshot

Viscoelastic multiscaling in immersed networks

inferredcites →https://doi.org/10.1126/science.1153878openalex-snapshot

An in Vivo Map of the Yeast Protein Interactome

inferredcites →https://doi.org/10.1126/science.aao5654openalex-snapshot

Phase separation of a yeast prion protein promotes cellular fitness

inferredcites →https://doi.org/10.1126/science.aaw8653openalex-snapshot

Valence and patterning of aromatic residues determine the phase behavior of prion-like domains

inferredcites →https://doi.org/10.1152/ajpcell.00438.2010openalex-snapshot

Biophysical properties of normal and diseased renal glomeruli

inferredcites →https://doi.org/10.1242/jcs.041137openalex-snapshot

The yeast endocytic protein Epsin 2 functions in a cell-division signaling pathway

inferredcites →https://doi.org/10.1242/jcs.115.8.1703openalex-snapshot

Sla1p couples the yeast endocytic machinery to proteins regulating actin dynamics

inferredcites →https://doi.org/10.1371/journal.pcbi.1002892openalex-snapshot

Membrane Sculpting by F-BAR Domains Studied by Molecular Dynamics Simulations

inferredcites →https://doi.org/10.1371/journal.pcbi.1003144openalex-snapshot

Structural Disorder Provides Increased Adaptability for Vesicle Trafficking Pathways

inferredcites →https://doi.org/10.1371/journal.pone.0103311openalex-snapshot

An Abp1-Dependent Route of Endocytosis Functions when the Classical Endocytic Pathway in Yeast Is Inhibited

inferredcites →https://doi.org/10.71781/30316openalex-snapshot

The regulation and induction of clathrin-mediated endocytosis through a protein aqueous-aqueous phase separation mechanism

inferredcites →https://doi.org/10.7554/elife.06807openalex-snapshot

Promiscuous interactions and protein disaggregases determine the material state of stress-inducible RNP granules

inferredcites →https://doi.org/10.7554/elife.21455openalex-snapshot

The synaptonemal complex has liquid crystalline properties and spatially regulates meiotic recombination factors

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4785780openalex-extracted

Biomolecular Condensates are Defined by Interphase Electric Potentials

inferred← citeshttps://doi.org/10.1002/advs.202309864openalex-snapshot

Photoswitchable Endocytosis of Biomolecular Condensates in Giant Vesicles

inferred← citeshttps://doi.org/10.1002/advs.202524219openalex-snapshot

Crystal Facet‐Polysaccharide Matching in CFS‐P Nanocrystals Drives Fungal Uptake, Vacuole Destruction, and Selective Antifungal Activity

inferred← citeshttps://doi.org/10.1002/pro.70192openalex-snapshot

Biomolecular condensates—Prerequisites for anhydrobiosis?

inferred← citeshttps://doi.org/10.1002/smll.202501470openalex-snapshot

Dynamic Duos: Coacervate‐Lipid Membrane Interactions in Regulating Membrane Transformation and Condensate Size

inferred← citeshttps://doi.org/10.1002/smtd.202300294openalex-snapshot

Interfacing Coacervates with Membranes: From Artificial Organelles and Hybrid Protocells to Intracellular Delivery

inferred← citeshttps://doi.org/10.1007/978-3-032-06936-8_9openalex-snapshot

Biomolecular Condensates in and Around the ER–Golgi Interface

inferred← citeshttps://doi.org/10.1007/s11120-022-00922-xopenalex-snapshot

Reactive oxygen species in photosystem II: relevance for oxidative signaling

inferred← citeshttps://doi.org/10.1007/s11120-023-01063-5openalex-snapshot

Peculiarities of DNP-INT and DBMIB as inhibitors of the photosynthetic electron transport

inferred← citeshttps://doi.org/10.1007/s12551-025-01326-6openalex-snapshot

The rheology and interfacial properties of biomolecular condensates

inferred← citeshttps://doi.org/10.1007/s12551-026-01464-5openalex-snapshot

Biophysical determinants of membranotropism: how proteins and peptides recognize, insert into, and remodel lipid bilayers

inferred← citeshttps://doi.org/10.1007/s40242-023-3175-1openalex-snapshot

Molecular Insights into Distinct Membrane-insertion Behaviors and Mechanisms of 20 Amino Acids: an All-atom MD Simulation Study

inferred← citeshttps://doi.org/10.1016/j.bbamem.2021.183684openalex-snapshot

Lipids, membranes, colloids and cells: A long view

inferred← citeshttps://doi.org/10.1016/j.bbamem.2023.184121openalex-snapshot

Membrane reshaping by protein condensates

inferred← citeshttps://doi.org/10.1016/j.bbrc.2025.151489openalex-snapshot

Zinc ions trigger the prion protein liquid-liquid phase separation

inferred← citeshttps://doi.org/10.1016/j.biochi.2024.08.002openalex-snapshot

Behind the stoNE wall: A fervent activity for nuclear lipids

inferred← citeshttps://doi.org/10.1016/j.bpj.2023.12.023openalex-snapshot

Coupling liquid phases in 3D condensates and 2D membranes: Successes, challenges, and tools

inferred← citeshttps://doi.org/10.1016/j.bpj.2024.04.031openalex-snapshot

Protein condensates in the the secretory pathway: Unraveling biophysical interactions and function

inferred← citeshttps://doi.org/10.1016/j.bpj.2025.10.009openalex-snapshot

Mechanical regulation and activity of nuclear condensates

inferred← citeshttps://doi.org/10.1016/j.bpj.2026.03.037openalex-snapshot

Computational rheometry for modeling viscoelasticity and mechanical responses of biomolecular condensates

inferred← citeshttps://doi.org/10.1016/j.ceb.2022.102132openalex-snapshot

Myosin motors in sensory hair bundle assembly

inferred← citeshttps://doi.org/10.1016/j.ceb.2023.102258openalex-snapshot

Protein condensates as flexible platforms for membrane traffic

inferred← citeshttps://doi.org/10.1016/j.ceb.2024.102393openalex-snapshot

Biomolecular condensates as drivers of membrane trafficking and remodelling

inferred← citeshttps://doi.org/10.1016/j.cell.2023.08.032openalex-snapshot

A disordered region controls cBAF activity via condensation and partner recruitment

inferred← citeshttps://doi.org/10.1016/j.cell.2024.02.029openalex-snapshot

Macromolecular condensation organizes nucleolar sub-phases to set up a pH gradient

inferred← citeshttps://doi.org/10.1016/j.cell.2024.07.034openalex-snapshot

Condensate interfacial forces reposition DNA loci and probe chromatin viscoelasticity

inferred← citeshttps://doi.org/10.1016/j.celrep.2023.113076openalex-snapshot

Anillin forms linear structures and facilitates furrow ingression after septin and formin depletion

inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114373openalex-snapshot

The condensation of HP1α/Swi6 imparts nuclear stiffness

inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114725openalex-snapshot

Cross-regulations of two connected domains form a mechanical circuit for steady force transmission during clathrin-mediated endocytosis

inferred← citeshttps://doi.org/10.1016/j.conb.2022.01.004openalex-snapshot

Endocytic proteins: An expanding repertoire of presynaptic functions

inferred← citeshttps://doi.org/10.1016/j.dnarep.2021.103179openalex-snapshot

Biomolecular condensates at sites of DNA damage: More than just a phase

inferred← citeshttps://doi.org/10.1016/j.jbc.2025.108548openalex-snapshot

Phase separation as a key mechanism in plant development, environmental adaptation, and abiotic stress response

inferred← citeshttps://doi.org/10.1016/j.jbc.2025.110834openalex-snapshot

Endophilin–lamellipodin–VASP, key components in fast endophilin–mediated endocytosis, control actin polymerization within liquid-like condensates

inferred← citeshttps://doi.org/10.1016/j.jcis.2022.08.051openalex-snapshot

Dilatational and shear rheology of soluble and insoluble monolayers with a Langmuir trough

inferred← citeshttps://doi.org/10.1016/j.jcis.2024.04.136openalex-snapshot

Influence of pH and lipid membrane on the liquid–liquid phase separation of wheat γ-gliadin in aqueous conditions

inferred← citeshttps://doi.org/10.1016/j.jmb.2023.167971openalex-snapshot

Phase Separation in Biology and Disease; Current Perspectives and Open Questions

inferred← citeshttps://doi.org/10.1016/j.jmb.2023.168380openalex-snapshot

Biomolecular Condensates as Novel Antiviral Targets

inferred← citeshttps://doi.org/10.1016/j.jmb.2024.168574openalex-snapshot

Selective Autophagy of Macromolecular Complexes: What Does It Take to be Taken?

inferred← citeshttps://doi.org/10.1016/j.jmb.2025.168953openalex-snapshot

Disordered Regions of Condensate-promoting Proteins Have Distinct Molecular Signatures Associated with Cellular Function

inferred← citeshttps://doi.org/10.1016/j.molcel.2022.05.018openalex-snapshot

A conceptual framework for understanding phase separation and addressing open questions and challenges

inferred← citeshttps://doi.org/10.1016/j.molcel.2026.01.009openalex-snapshot

Density transitions in the regulation of transcription

inferred← citeshttps://doi.org/10.1016/j.molcel.2026.07.008openalex-snapshot

Biomolecular condensates can function as inherent catalysts

inferred← citeshttps://doi.org/10.1016/j.pbi.2025.102740openalex-snapshot

Wet scissors: How biomolecular condensates cut cellular membranes

inferred← citeshttps://doi.org/10.1016/j.tibs.2022.04.005openalex-snapshot

SRC homology 3 domains: multifaceted binding modules

inferred← citeshttps://doi.org/10.1016/j.tibs.2022.09.008openalex-snapshot

Let’s phase it: viruses are master architects of biomolecular condensates

inferred← citeshttps://doi.org/10.1016/j.tibs.2024.02.005openalex-snapshot

Protein–membrane interactions: sensing and generating curvature

inferred← citeshttps://doi.org/10.1016/j.tips.2022.07.001openalex-snapshot

Biomolecular condensates: new opportunities for drug discovery and RNA therapeutics

inferred← citeshttps://doi.org/10.1016/j.xplc.2023.100663openalex-snapshot

Liquid–liquid phase separation in plants: Advances and perspectives from model species to crops

inferred← citeshttps://doi.org/10.1021/acs.chemrev.2c00608openalex-snapshot

A New Phase of Networking: The Molecular Composition and Regulatory Dynamics of Mammalian Stress Granules

inferred← citeshttps://doi.org/10.1021/acs.chemrev.2c00814openalex-snapshot

Phase Transitions of Associative Biomacromolecules

inferred← citeshttps://doi.org/10.1021/acs.chemrev.4c00138openalex-snapshot

Fundamental Aspects of Phase-Separated Biomolecular Condensates

inferred← citeshttps://doi.org/10.1021/acs.iecr.3c03830openalex-snapshot

Complex Coacervate-Based Materials for Biomedicine: Recent Advancements and Future Prospects

inferred← citeshttps://doi.org/10.1021/acs.jpcb.3c08149openalex-snapshot

Sequence Sensitivity in Membrane Remodeling by Polyampholyte Condensates

inferred← citeshttps://doi.org/10.1021/acs.jpclett.3c00705openalex-snapshot

Coacervation-Induced Remodeling of Nanovesicles

inferred← citeshttps://doi.org/10.1021/acs.langmuir.6c02295openalex-snapshot

Membrane-Mediated Interaction of Biomolecular Condensates at Biomembranes

inferred← citeshttps://doi.org/10.1021/acs.nanolett.3c02915openalex-snapshot

Electric Potential at the Interface of Membraneless Organelles Gauged by Graphene

inferred← citeshttps://doi.org/10.1021/acs.nanolett.3c04169openalex-snapshot

Lipid Membrane Topographies Are Regulators for the Spatial Distribution of Liquid Protein Condensates

inferred← citeshttps://doi.org/10.1021/jacs.2c04096openalex-snapshot

Endocytosis of Coacervates into Liposomes

inferred← citeshttps://doi.org/10.1021/jacs.4c08946openalex-snapshot

Biomolecular Condensates are Characterized by Interphase Electric Potentials

inferred← citeshttps://doi.org/10.1038/s41467-021-24727-zopenalex-snapshot

A multi-step nucleation process determines the kinetics of prion-like domain phase separation

inferred← citeshttps://doi.org/10.1038/s41467-022-32529-0openalex-snapshot

Multivalent interactions between molecular components involved in fast endophilin mediated endocytosis drive protein phase separation

inferred← citeshttps://doi.org/10.1038/s41467-022-35176-7openalex-snapshot

The dynamic clustering of insulin receptor underlies its signaling and is disrupted in insulin resistance

inferred← citeshttps://doi.org/10.1038/s41467-022-35370-7openalex-snapshot

Condensates formed by prion-like low-complexity domains have small-world network structures and interfaces defined by expanded conformations

inferred← citeshttps://doi.org/10.1038/s41467-023-35847-zopenalex-snapshot

Different pathways for engulfment and endocytosis of liquid droplets by nanovesicles

inferred← citeshttps://doi.org/10.1038/s41467-023-37955-2openalex-snapshot

Wetting and complex remodeling of membranes by biomolecular condensates

inferred← citeshttps://doi.org/10.1038/s41467-023-41274-xopenalex-snapshot

Phase separation of protein mixtures is driven by the interplay of homotypic and heterotypic interactions

inferred← citeshttps://doi.org/10.1038/s41467-023-41709-5openalex-snapshot

Biomolecular condensates modulate membrane lipid packing and hydration

inferred← citeshttps://doi.org/10.1038/s41467-023-42372-6openalex-snapshot

Synapsin condensation controls synaptic vesicle sequestering and dynamics

inferred← citeshttps://doi.org/10.1038/s41467-023-44539-7openalex-snapshot

Membrane transformations of fusion and budding

inferred← citeshttps://doi.org/10.1038/s41467-024-47602-zopenalex-snapshot

Biomolecular condensates form spatially inhomogeneous network fluids

inferred← citeshttps://doi.org/10.1038/s41467-024-49222-zopenalex-snapshot

Membrane-induced 2D phase separation of the focal adhesion protein talin

inferred← citeshttps://doi.org/10.1038/s41467-025-57985-2openalex-snapshot

Lipid packing and cholesterol content regulate membrane wetting and remodeling by biomolecular condensates

inferred← citeshttps://doi.org/10.1038/s41467-025-62055-8openalex-snapshot

Current practices in the study of biomolecular condensates: a community comment

inferred← citeshttps://doi.org/10.1038/s41556-024-01354-6openalex-snapshot

Biomolecular condensation orchestrates clathrin-mediated endocytosis in plants

inferred← citeshttps://doi.org/10.1038/s41567-024-02558-1openalex-snapshot

Sequence-specific interactions determine viscoelasticity and ageing dynamics of protein condensates

inferred← citeshttps://doi.org/10.1038/s41567-025-02827-7openalex-snapshot

Single-fluorogen imaging reveals distinct environmental and structural features of biomolecular condensates

inferred← citeshttps://doi.org/10.1038/s41580-023-00673-0openalex-snapshot

The molecular basis for cellular function of intrinsically disordered protein regions

inferred← citeshttps://doi.org/10.1038/s41586-022-05138-6openalex-snapshot

Capillary forces generated by biomolecular condensates

inferred← citeshttps://doi.org/10.1038/s41586-023-05990-0openalex-snapshot

Visualizing the disordered nuclear transport machinery in situ

inferred← citeshttps://doi.org/10.1038/s41586-023-06044-1openalex-snapshot

Peroxisome biogenesis initiated by protein phase separation

inferred← citeshttps://doi.org/10.1038/s41586-023-06626-zopenalex-snapshot

Macromolecular condensation buffers intracellular water potential

inferred← citeshttps://doi.org/10.1038/s41586-024-07990-0openalex-snapshot

Biomolecular condensates mediate bending and scission of endosome membranes

inferred← citeshttps://doi.org/10.1038/s41589-022-01175-4openalex-snapshot

Molecular and environmental determinants of biomolecular condensate formation

inferred← citeshttps://doi.org/10.1038/s41594-026-01868-7openalex-snapshot

Unstructured but constructive FG repeats shape the nuclear pore complex architecture

inferred← citeshttps://doi.org/10.1038/s41598-022-22680-5openalex-snapshot

Membrane mediated phase separation of the bacterial nucleoid occlusion protein Noc

inferred← citeshttps://doi.org/10.1038/s42004-025-01502-5openalex-snapshot

Backbone-mediated weakening of pairwise interactions enables percolation in peptide-based mimics of protein condensates

inferred← citeshttps://doi.org/10.1038/s42005-022-01104-wopenalex-snapshot

Mutual remodeling of interacting nanodroplets and vesicles

inferred← citeshttps://doi.org/10.1038/s42005-024-01670-1openalex-snapshot

Control of cell membrane receptor condensation by adhesion to supported bilayers with nanoscale topography

inferred← citeshttps://doi.org/10.1039/d2sc02013kopenalex-snapshot

Coacervation of poly-electrolytes in the presence of lipid bilayers: mutual alteration of structure and morphology

inferred← citeshttps://doi.org/10.1039/d3na00073gopenalex-snapshot

Sequence-dependent fusion dynamics and physical properties of DNA droplets

inferred← citeshttps://doi.org/10.1039/d3sm00131hopenalex-snapshot

Membrane curvature sensing by model biomolecular condensates

inferred← citeshttps://doi.org/10.1039/d5sm00585jopenalex-snapshot

Complex remodeling of biomembranes and vesicles by condensate droplets

inferred← citeshttps://doi.org/10.1039/d5sm00740bopenalex-snapshot

Biomolecular condensate microstructure is invariant to sequence-encoded molecular and macroscopic properties

inferred← citeshttps://doi.org/10.1063/5.0223001openalex-snapshot

Direct computations of viscoelastic moduli of biomolecular condensates

inferred← citeshttps://doi.org/10.1073/pnas.2424126123openalex-snapshot

Condensate-mediated shape transformations of cellular membranes by capillary forces

inferred← citeshttps://doi.org/10.1073/pnas.2424135122openalex-snapshot

Material properties of biomolecular condensates emerge from nanoscale dynamics

inferred← citeshttps://doi.org/10.1073/pnas.2515427122openalex-snapshot

Disulfide cross-linked redox-sensitive peptide condensates are efficient cell delivery vehicles of molecular cargo

inferred← citeshttps://doi.org/10.1080/19491034.2024.2319957openalex-snapshot

Emergent microenvironments of nucleoli

inferred← citeshttps://doi.org/10.1088/1361-6633/ae12a7openalex-snapshot

Physics of droplet regulation in biological cells

inferred← citeshttps://doi.org/10.1088/1674-1056/adc36dopenalex-snapshot

Shape transformation of vesicles induced by orientational arrangement of membrane proteins

inferred← citeshttps://doi.org/10.1093/plcell/koad177openalex-snapshot

Protein phase separation in plant membrane biology: more than just a compartmentalization strategy

inferred← citeshttps://doi.org/10.1101/2022.05.21.492916openalex-snapshot

Condensates of disordered proteins have small-world network structures and interfaces defined by expanded conformations

inferred← citeshttps://doi.org/10.1101/2022.07.07.499201openalex-snapshot

Deciphering the conformations and dynamics of FG-nucleoporins in situ

inferred← citeshttps://doi.org/10.1101/2023.02.27.530281openalex-snapshot

Condensate-driven interfacial forces reposition DNA loci and measure chromatin viscoelasticity

inferred← citeshttps://doi.org/10.1101/2023.03.15.532828openalex-snapshot

Phase Separation in Mixtures of Prion-Like Low Complexity Domains is Driven by the Interplay of Homotypic and Heterotypic Interactions

inferred← citeshttps://doi.org/10.1101/2023.03.31.535113openalex-snapshot

Membrane-induced 2D phase separation of focal adhesion proteins

inferred← citeshttps://doi.org/10.1101/2024.07.06.602359openalex-snapshot

Condenzymes: Biomolecular condensates with inherent catalytic activities

inferred← citeshttps://doi.org/10.1101/2024.10.01.616068openalex-snapshot

Two-dimensional HRS condensates drive the assembly of flat clathrin lattices on endosomes

inferred← citeshttps://doi.org/10.1101/2024.12.01.626236openalex-snapshot

Charge distribution of coating brush drives inter-chromosome attraction

inferred← citeshttps://doi.org/10.1101/2025.03.25.645354openalex-snapshot

Biomolecular condensate microstructure couples molecular and mesoscale properties

inferred← citeshttps://doi.org/10.1101/2025.08.20.671282openalex-snapshot

Computational rheometry of viscoelastic networks: From random graphs to biomolecular condensates

inferred← citeshttps://doi.org/10.1103/41fd-r847openalex-snapshot

Charge distribution of the coating brush drives interchromosome attraction

inferred← citeshttps://doi.org/10.1103/kx13-czqbopenalex-snapshot

Liquid-Liquid Phase Separation Enables Highly Selective Viral Genome Packaging

inferred← citeshttps://doi.org/10.1103/physreve.106.044412openalex-snapshot

Phase separation and critical size in molecular sorting

inferred← citeshttps://doi.org/10.1111/jnc.15586openalex-snapshot

Phase separation of the mammalian prion protein: Physiological and pathological perspectives

inferred← citeshttps://doi.org/10.1126/sciadv.adg0432openalex-snapshot

A bending rigidity parameter for stress granule condensates

inferred← citeshttps://doi.org/10.1126/sciadv.adi1535openalex-snapshot

Force redistribution in clathrin-mediated endocytosis revealed by coiled-coil force sensors

inferred← citeshttps://doi.org/10.1126/sciadv.adi7347openalex-snapshot

Copper drives prion protein phase separation and modulates aggregation

inferred← citeshttps://doi.org/10.1126/sciadv.adv7875openalex-snapshot

Active transport enables protein condensation in cells

inferred← citeshttps://doi.org/10.1126/sciadv.ady4934openalex-snapshot

Linear ubiquitination triggers Amph-mediated T-tubule biogenesis

inferred← citeshttps://doi.org/10.1126/science.adv6588openalex-snapshot

Multiscale structure of chromatin condensates explains phase separation and material properties

inferred← citeshttps://doi.org/10.1146/annurev-arplant-070225-034846openalex-snapshot

Pyrenoid Structure, Function, Evolution, and Characterization Across Diverse Lineages

inferred← citeshttps://doi.org/10.1146/annurev-biophys-030722-121518openalex-snapshot

Biomolecular Condensates in Contact with Membranes

inferred← citeshttps://doi.org/10.1146/annurev-virology-093020-013659openalex-snapshot

Liquid Phase Partitioning in Virus Replication: Observations and Opportunities

inferred← citeshttps://doi.org/10.1186/s12915-026-02615-6openalex-snapshot

Plasma membrane invaginations and their diverse cellular functions

inferred← citeshttps://doi.org/10.1242/jcs.261413openalex-snapshot

Dipping contacts – a novel type of contact site at the interface between membraneless organelles and membranes

inferred← citeshttps://doi.org/10.1242/jcs.264222openalex-snapshot

Clathrin-mediated endocytosis in budding yeast at a glance: animated

inferred← citeshttps://doi.org/10.1371/journal.ppat.1011228openalex-snapshot

Understanding the link between the actin cytoskeleton and prion biology

inferred← citeshttps://doi.org/10.1515/mim-2024-0018openalex-snapshot

Perspective: fluorescence lifetime imaging and single-molecule spectroscopy for studying biological condensates

inferred← citeshttps://doi.org/10.3233/jpd-230183openalex-snapshot

Defining a Lewy Body: Running Up the Hill of Shifting Definitions and Evolving Concepts

inferred← citeshttps://doi.org/10.3389/fcell.2022.896305openalex-snapshot

The Molecular and Functional Interaction Between Membrane-Bound Organelles and Membrane-Less Condensates

inferred← citeshttps://doi.org/10.3389/fcimb.2023.1082622openalex-snapshot

Refractile bodies of Eimeria tenella are proteinaceous membrane-less organelles that undergo dynamic changes during infection

inferred← citeshttps://doi.org/10.3389/fmicb.2021.751880openalex-snapshot

Liquid-Liquid Phase Separation: Unraveling the Enigma of Biomolecular Condensates in Microbial Cells

inferred← citeshttps://doi.org/10.3389/frsfm.2023.1339496openalex-snapshot

pH-dependent interactions of coacervate-forming histidine-rich peptide with model lipid membranes

inferred← citeshttps://doi.org/10.3390/biom13060926openalex-snapshot

Leaflet Tensions Control the Spatio-Temporal Remodeling of Lipid Bilayers and Nanovesicles

inferred← citeshttps://doi.org/10.3390/ijms25074127openalex-snapshot

Biomolecular Condensates Decipher Molecular Codes of Cell Fate: From Biophysical Fundamentals to Therapeutic Practices

inferred← citeshttps://doi.org/10.3390/membranes13020223openalex-snapshot

Remodeling of Biomembranes and Vesicles by Adhesion of Condensate Droplets

inferred← citeshttps://doi.org/10.3390/v16030474openalex-snapshot

A Balancing Act: The Viral–Host Battle over RNA Binding Proteins

inferred← citeshttps://doi.org/10.5483/bmbrep.2022.55.8.101openalex-snapshot

Recent trends in studies of biomolecular phase separation.

inferred← citeshttps://doi.org/10.64898/2026.06.09.731149openalex-snapshot

A bifunctional coiled-coil protein generates the membrane-within-condensate architecture of the CO 2 -fixing pyrenoid

inferred← citeshttps://doi.org/10.64898/2026.06.22.731667openalex-snapshot

Nanocondensate tunnelling

inferred← citeshttps://doi.org/10.64898/2026.09.17.752504openalex-snapshot

Phosphoregulation of hierarchical protein condensate formation during clathrin-mediated endocytosis

inferred← citeshttps://doi.org/10.70675/7f52cc90zd498z4d0cz9783z803a0c5a65bbopenalex-snapshot

Droplet-based microfluidics to investigate wheat gliadins phase behavior within lipid vesicles

inferred← citeshttps://doi.org/10.7554/elife.72865openalex-snapshot

Condensation of Ede1 promotes the initiation of endocytosis

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.