ArticleJournal of the American Chemical Society2026
Patchy Membrane-Directed Multiphase Complex Coacervation.
Article in Journal of the American Chemical Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
Abstract
Multiphase separation is a key feature in biomolecular condensates to regulate biological function. In cells, phase separation can occur in a bulk solution or on a lipid membrane. To establish life-like features in artificial cells, much research has been carried out to reproduce multiphase separation behavior. However, this has been mostly restricted to bulk properties, whereas membrane interactions are much less investigated. Here, we introduce a membrane-based strategy in which interfacial electrostatic heterogeneity governs multiphase separation in amylose-based coacervates, enabling the formation of subcompartments localized near the membrane interface. By integrating bowl-shaped polymer vesicles (stomatocytes) decorated with negatively charged gold nanoparticles into a terpolymer membrane, we construct a patchy membrane architecture that introduces localized, highly charged interfacial domains, thereby stabilizing amylose-based coacervates. Upon the addition of succinylated bovine serum albumin as a second phase-forming component, the embedded stomatocytes allow precise control over multiphase separation. Modulating the stomatocytes' coverage at the coacervate interface enables systematic tuning of the size, spatial localization, and number of protein-enriched subdroplets. Complete stomatocyte coverage further enhances multiphase stability against variations in ionic strength and pH, while improving long-term storage stability. Moreover, the interfacial multiphase organization can be dynamically regulated by ionic strength and temperature. Furthermore, the enlarged interfacial area promotes enhanced cargo uptake, while the programmable positioning of enzyme-containing subcompartments enables spatial regulation of interprotocellular chemical communication. Together, these findings establish interfacial electrostatic heterogeneity as a versatile strategy for engineering membrane-associated multiphase protocells in which spatial organization governs molecular transport, catalysis, and communication.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.