{"title":"Diffusive exit rates through pores in membrane-enclosed structures.","authors":"Zitao Yang, Elena F Koslover","doi":"10.1088/1478-3975/acb1ea","DOIUrl":null,"url":null,"abstract":"<p><p>The function of many membrane-enclosed intracellular structures relies on release of diffusing particles that exit through narrow pores or channels in the membrane. The rate of release varies with pore size, density, and length of the channel. We propose a simple approximate model, validated with stochastic simulations, for estimating the effective release rate from cylinders, and other simple-shaped domains, as a function of channel parameters. The results demonstrate that, for very small pores, a low density of channels scattered over the boundary is sufficient to achieve substantial rates of particle release. Furthermore, we show that increasing the length of passive channels will both reduce release rates and lead to a less steep dependence on channel density. Our results are compared to previously-measured local calcium release rates from tubules of the endoplasmic reticulum, providing an estimate of the relevant channel density responsible for the observed calcium efflux.</p>","PeriodicalId":20207,"journal":{"name":"Physical biology","volume":null,"pages":null},"PeriodicalIF":2.0000,"publicationDate":"2023-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physical biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1088/1478-3975/acb1ea","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 1
Abstract
The function of many membrane-enclosed intracellular structures relies on release of diffusing particles that exit through narrow pores or channels in the membrane. The rate of release varies with pore size, density, and length of the channel. We propose a simple approximate model, validated with stochastic simulations, for estimating the effective release rate from cylinders, and other simple-shaped domains, as a function of channel parameters. The results demonstrate that, for very small pores, a low density of channels scattered over the boundary is sufficient to achieve substantial rates of particle release. Furthermore, we show that increasing the length of passive channels will both reduce release rates and lead to a less steep dependence on channel density. Our results are compared to previously-measured local calcium release rates from tubules of the endoplasmic reticulum, providing an estimate of the relevant channel density responsible for the observed calcium efflux.
期刊介绍:
Physical Biology publishes articles in the broad interdisciplinary field bridging biology with the physical sciences and engineering. This journal focuses on research in which quantitative approaches – experimental, theoretical and modeling – lead to new insights into biological systems at all scales of space and time, and all levels of organizational complexity.
Physical Biology accepts contributions from a wide range of biological sub-fields, including topics such as:
molecular biophysics, including single molecule studies, protein-protein and protein-DNA interactions
subcellular structures, organelle dynamics, membranes, protein assemblies, chromosome structure
intracellular processes, e.g. cytoskeleton dynamics, cellular transport, cell division
systems biology, e.g. signaling, gene regulation and metabolic networks
cells and their microenvironment, e.g. cell mechanics and motility, chemotaxis, extracellular matrix, biofilms
cell-material interactions, e.g. biointerfaces, electrical stimulation and sensing, endocytosis
cell-cell interactions, cell aggregates, organoids, tissues and organs
developmental dynamics, including pattern formation and morphogenesis
physical and evolutionary aspects of disease, e.g. cancer progression, amyloid formation
neuronal systems, including information processing by networks, memory and learning
population dynamics, ecology, and evolution
collective action and emergence of collective phenomena.