Mitochondrial Network Branching Enables Rapid Protein Spread with Slower Mitochondrial Dynamics

Mitochondrial network structure is controlled by the dynamical processes of fusion and fission, which merge and split mitochondrial tubes into structures including branches and loops. To investigate the impact of mitochondrial network dynamics and structure on the spread of proteins and other molecules through mitochondrial networks, we used stochastic simulations of two distinct quantitative models that each included mitochondrial fusion and fission, and particle diffusion via the network. Better-connected mitochondrial networks and networks with faster dynamics exhibit more rapid particle spread on the network, with little further improvement once a network has become well connected. As fragmented networks gradually become better connected, particle spread either steadily improves until the networks become well connected for slow-diffusing particles or plateaus for fast-diffusing particles. We compared model mitochondrial networks with both end-to-end and end-to-side fusion, which form branches, to nonbranching model networks that lack end-to-side fusion. To achieve the optimum (most rapid) spread that occurs on well-connected branching networks, nonbranching networks require much faster fusion and fission dynamics. Thus, the process of end-to-side fusion, which creates branches in mitochondrial networks, enables rapid spread of particles on the network with relatively slow fusion and fission dynamics. This modeling of protein spread on mitochondrial networks builds toward mechanistic understanding of how mitochondrial structure and dynamics regulate mitochondrial function. Published by the American Physical Society 2024

Authors

Institutions

Publication Details

Journal
PRX Life
Published
2024-10-22
DOI
https://doi.org/10.1103/prxlife.2.043005
Citations
7
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
1.64

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Mitochondrial Network Branching Enables Rapid Protein Spread with Slower Mitochondrial Dynamics

Aidan I. Brown, Sean P. Cornelius, Prabha Chuphal, Jordan D. Lanctôt
7 citations
PRX Life
Mitochondrial Function and Pathology
1.64
article

Mitochondrial Network Branching Enables Rapid Protein Spread with Slower Mitochondrial Dynamics

Aidan I. Brown, Sean P. Cornelius, Prabha Chuphal, Jordan D. Lanctôt
article en
7 citations

Abstract

Mitochondrial network structure is controlled by the dynamical processes of fusion and fission, which merge and split mitochondrial tubes into structures including branches and loops. To investigate the impact of mitochondrial network dynamics and structure on the spread of proteins and other molecules through mitochondrial networks, we used stochastic simulations of two distinct quantitative models that each included mitochondrial fusion and fission, and particle diffusion via the network. Better-connected mitochondrial networks and networks with faster dynamics exhibit more rapid particle spread on the network, with little further improvement once a network has become well connected. As fragmented networks gradually become better connected, particle spread either steadily improves until the networks become well connected for slow-diffusing particles or plateaus for fast-diffusing particles. We compared model mitochondrial networks with both end-to-end and end-to-side fusion, which form branches, to nonbranching model networks that lack end-to-side fusion. To achieve the optimum (most rapid) spread that occurs on well-connected branching networks, nonbranching networks require much faster fusion and fission dynamics. Thus, the process of end-to-side fusion, which creates branches in mitochondrial networks, enables rapid spread of particles on the network with relatively slow fusion and fission dynamics. This modeling of protein spread on mitochondrial networks builds toward mechanistic understanding of how mitochondrial structure and dynamics regulate mitochondrial function. Published by the American Physical Society 2024

PRX LifeVol. 2(4)
Toronto Metropolitan University (CA)
Alliance de recherche numérique du Canada, Natural Sciences and Engineering Research Council of Canada
Openalex Percentile: Top 16%
Mitochondrial Function and Pathology
1.64
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.