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<p>Biological membranes are not passive barriers; they are active information-processing surfaces. This article introduces the <i>Membrane Information Organization (MIO)</i> framework, which defines how the spatial geometry and molecular composition of membranes co-regulate signal fidelity. MIO proposes that when regions of mechanical stability (e.g., minimized bending energy) overlap with zones of high signaling efficiency, membranes act as dynamic hubs that guide cellular behavior. We synthesize experimental findings across multiple systems, from immune synapses and stem cell niches to cardiac pacemakers and tumor fronts, to show that nanoscale membrane domains (rafts, scaffolds, curvature sensors) orchestrate decisions like cell polarity, fate selection, and rhythmic synchronization. Disruption of this organization leads to measurable dysfunction: in Alzheimer’s, mislocalized lipid rafts degrade synaptic signaling; in cancer, altered Ras/EGFR clustering enhances growth signals and therapeutic resistance; in autoimmune disease, malformed membrane domains trigger self-directed attack. MIO offers a unifying language to compare these diverse systems by combining spatial maps of mechanical and informational cues. It introduces simple, testable predictions: enhancing membrane order improves signaling precision; dispersing curvature scaffolds impairs cellular coordination. This logic applies to both natural systems and synthetic platforms, including programmable liposomes, bioelectronic interfaces, and implantable neural sensors. Rather than replacing prior models, MIO integrates them under a quantitative, cross-scale perspective. Aligning structure with signaling function opens new directions for diagnostics, therapeutics, and the engineering of living systems.</p>

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Cell membranes and the organization of biological information

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年11月8日

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  • Seyed Kiarash Sadat Rafiei,
  • Mahsa Asadi Anar

摘要

Biological membranes are not passive barriers; they are active information-processing surfaces. This article introduces the Membrane Information Organization (MIO) framework, which defines how the spatial geometry and molecular composition of membranes co-regulate signal fidelity. MIO proposes that when regions of mechanical stability (e.g., minimized bending energy) overlap with zones of high signaling efficiency, membranes act as dynamic hubs that guide cellular behavior. We synthesize experimental findings across multiple systems, from immune synapses and stem cell niches to cardiac pacemakers and tumor fronts, to show that nanoscale membrane domains (rafts, scaffolds, curvature sensors) orchestrate decisions like cell polarity, fate selection, and rhythmic synchronization. Disruption of this organization leads to measurable dysfunction: in Alzheimer’s, mislocalized lipid rafts degrade synaptic signaling; in cancer, altered Ras/EGFR clustering enhances growth signals and therapeutic resistance; in autoimmune disease, malformed membrane domains trigger self-directed attack. MIO offers a unifying language to compare these diverse systems by combining spatial maps of mechanical and informational cues. It introduces simple, testable predictions: enhancing membrane order improves signaling precision; dispersing curvature scaffolds impairs cellular coordination. This logic applies to both natural systems and synthetic platforms, including programmable liposomes, bioelectronic interfaces, and implantable neural sensors. Rather than replacing prior models, MIO integrates them under a quantitative, cross-scale perspective. Aligning structure with signaling function opens new directions for diagnostics, therapeutics, and the engineering of living systems.