Paper List
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Ill-Conditioning in Dictionary-Based Dynamic-Equation Learning: A Systems Biology Case Study
This paper addresses the critical challenge of numerical ill-conditioning and multicollinearity in library-based sparse regression methods (e.g., SIND...
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Hybrid eTFCE–GRF: Exact Cluster-Size Retrieval with Analytical pp-Values for Voxel-Based Morphometry
This paper addresses the computational bottleneck in voxel-based neuroimaging analysis by providing a method that delivers exact cluster-size retrieva...
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abx_amr_simulator: A simulation environment for antibiotic prescribing policy optimization under antimicrobial resistance
This paper addresses the critical challenge of quantitatively evaluating antibiotic prescribing policies under realistic uncertainty and partial obser...
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PesTwin: a biology-informed Digital Twin for enabling precision farming
This paper addresses the critical bottleneck in precision agriculture: the inability to accurately forecast pest outbreaks in real-time, leading to su...
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Equivariant Asynchronous Diffusion: An Adaptive Denoising Schedule for Accelerated Molecular Conformation Generation
This paper addresses the core challenge of generating physically plausible 3D molecular structures by bridging the gap between autoregressive methods ...
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Omics Data Discovery Agents
This paper addresses the core challenge of making published omics data computationally reusable by automating the extraction, quantification, and inte...
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Single-cell directional sensing at ultra-low chemoattractant concentrations from extreme first-passage events
This work addresses the core challenge of how a cell can rapidly and accurately determine the direction of a chemoattractant source when the signal is...
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SDSR: A Spectral Divide-and-Conquer Approach for Species Tree Reconstruction
This paper addresses the computational bottleneck in reconstructing species trees from thousands of species and multiple genes by introducing a scalab...
Stability analysis of action potential generation using Markov models of voltage‑gated sodium channel isoforms
School of Mathematics and Statistics, Rochester Institute of Technology | School of Physics, Rochester Institute of Technology | School of Physics and Astronomy & School of Mathematics and Statistics, Rochester Institute of Technology
30秒速读
IN SHORT: This work addresses the challenge of systematically characterizing how the high-dimensional parameter space of Markov models for different sodium channel isoforms influences the robustness and excitability of neuronal firing.
核心创新
- Methodology Integrates a six-state Markov model for nine human NaV isoforms with a simplified KV3.1 model, enabling a unified framework for isoform-specific stability analysis.
- Methodology Applies bifurcation theory and local stability analysis to map 'excitable landscapes' across the (g_Na, g_K) parameter space, visualizing regions supporting stable oscillatory behavior.
- Biology Quantitatively ranks NaV isoforms by their supported excitable regimes, identifying NaV1.3, 1.4, and 1.6 as broadly supportive and NaV1.7 and 1.9 as minimally oscillatory.
主要结论
- Isoforms NaV1.3, NaV1.4, and NaV1.6 support the broadest parameter regions for stable limit cycles (oscillatory firing), indicating their robustness in sustaining action potential trains.
- Isoforms NaV1.7 and NaV1.9 exhibit minimal oscillatory behavior across the tested conductance parameter space, correlating with their specialized roles in peripheral nociception.
- The hybrid Markov-HH modeling and stability analysis framework successfully narrows the vast parameter search space for designing synthetic excitable systems, moving from trial-and-error to principled design.
摘要: We investigate a conductance‑based neuron model to explore how voltage‑gated ion channel isoforms influence action‑potential generation. The model combines a six‑state Markov representation of NaV channels with a first‑order KV3.1 model, allowing us to vary maximal sodium and potassium conductances and compare nine NaV isoforms. Using bifurcation theory and local stability analysis, we map regions of stable limit cycles and visualize excitability landscapes via heatmap‑based diagrams. These analyses show that isoforms NaV1.3, NaV1.4 and NaV1.6 support broad excitable regimes, while isoforms NaV1.7 and NaV1.9 exhibit minimal oscillatory behavior. Our findings provide insights into the role of channel heterogeneity in neuronal dynamics and may help to guide the design of synthetic excitable systems by narrowing the parameter space needed for robust action‑potential trains.