Mehdi Bouzid, Cesar Valencia Gallardo, Magdalena Kopec, Lara Koehler, Giuseppe Foffi, Olivia du Roure, Julien Heuvingh, Martin Lenz
{"title":"Transient contacts between filaments impart its elasticity to branched actin","authors":"Mehdi Bouzid, Cesar Valencia Gallardo, Magdalena Kopec, Lara Koehler, Giuseppe Foffi, Olivia du Roure, Julien Heuvingh, Martin Lenz","doi":"arxiv-2409.00549","DOIUrl":null,"url":null,"abstract":"Branched actin networks exert pushing forces in eukaryotic cells, and adapt\ntheir stiffness to their environment. The physical basis for their mechanics\nand adaptability is however not understood. Indeed, here we show that their\nhigh density and low connectivity place them outside the scope of standard\nelastic network models for actin. We combine high-precision mechanical\nexperiments, molecular dynamics simulations and a mean-field elastic theory to\nshow that they are instead dominated by the proliferation of interfilament\ncontacts under compression. This places branched actin in the same category as\nundercoordinated, fibrous materials such as sheep's wool. When the network is\ngrown under force, filaments entangle as if knitted together and trap contacts\nin their structure. Trapped contacts play a similar role as crosslinkers in\nrigidifying the network, and are thus key to its active adaptive mechanics.","PeriodicalId":501170,"journal":{"name":"arXiv - QuanBio - Subcellular Processes","volume":"59 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Subcellular Processes","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2409.00549","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Branched actin networks exert pushing forces in eukaryotic cells, and adapt
their stiffness to their environment. The physical basis for their mechanics
and adaptability is however not understood. Indeed, here we show that their
high density and low connectivity place them outside the scope of standard
elastic network models for actin. We combine high-precision mechanical
experiments, molecular dynamics simulations and a mean-field elastic theory to
show that they are instead dominated by the proliferation of interfilament
contacts under compression. This places branched actin in the same category as
undercoordinated, fibrous materials such as sheep's wool. When the network is
grown under force, filaments entangle as if knitted together and trap contacts
in their structure. Trapped contacts play a similar role as crosslinkers in
rigidifying the network, and are thus key to its active adaptive mechanics.