Award Abstract # 1725065
Theory of dynamic cytoskeletal length regulation and stabilization

NSF Org: DMR
Division Of Materials Research
Recipient: THE REGENTS OF THE UNIVERSITY OF COLORADO
Initial Amendment Date: May 29, 2018
Latest Amendment Date: June 21, 2021
Award Number: 1725065
Award Instrument: Continuing Grant
Program Manager: Daryl Hess
dhess@nsf.gov
 (703)292-4942
DMR
 Division Of Materials Research
MPS
 Directorate for Mathematical and Physical Sciences
Start Date: June 15, 2018
End Date: May 31, 2022 (Estimated)
Total Intended Award Amount: $342,000.00
Total Awarded Amount to Date: $413,427.00
Funds Obligated to Date: FY 2018 = $228,000.00
FY 2020 = $114,000.00

FY 2021 = $71,427.00
History of Investigator:
  • Meredith Betterton (Principal Investigator)
    mdb@colorado.edu
Recipient Sponsored Research Office: University of Colorado at Boulder
3100 MARINE ST
Boulder
CO  US  80309-0001
(303)492-6221
Sponsor Congressional District: 02
Primary Place of Performance: University of Colorado at Boulder
Boulder
CO  US  80303-1058
Primary Place of Performance
Congressional District:
02
Unique Entity Identifier (UEI): SPVKK1RC2MZ3
Parent UEI:
NSF Program(s): DMR SHORT TERM SUPPORT,
CONDENSED MATTER & MAT THEORY
Primary Program Source: 01001819DB NSF RESEARCH & RELATED ACTIVIT
01002021DB NSF RESEARCH & RELATED ACTIVIT

01002122DB NSF RESEARCH & RELATED ACTIVIT
Program Reference Code(s): 102Z, 7573
Program Element Code(s): 171200, 176500
Award Agency Code: 4900
Fund Agency Code: 4900
Assistance Listing Number(s): 47.049

ABSTRACT

NONTECHNICAL SUMMARY
This award supports theoretical and computational research, and education on the fundamental mechanisms that determine size of living organisms and biomaterials. When biological organisms grow, they regulate the size that they reach: for example, people grow to their adult height and then remain that tall. Therefore, sensing and regulating size is an essential physics problem that biological organisms solve. Living systems control the size not just of whole organisms, but also of smaller internal structures (organs, cells, and structures inside cells). The physical principles and mechanisms underlying the sensing and control of size in biology are not well understood. This project will develop new physics-based models to understand and predict how length of one class of subcellular structures are regulated in organisms. Related mechanisms may be useful in regulating the growth of polymers and biomaterials. This project will develop interdisciplinary research and education, and work to improve diversity in science.

TECHNICAL SUMMARY
This award supports theoretical and computational research, and education on the fundamental mechanisms that determine size of living organisms and biomimetic biomaterials. Regulating physical size is an essential problem that biological organisms must solve, but the physical principles and mechanisms underlying the sensing and control of size in biology are not well understood. The regulation of polymer length is important for the organization of the cellular cytoskeleton, which affects the size of subcellular organelles such as the mitotic spindle and the structure of cells themselves. An important general question is how to use molecular-level information to understand and predict higher-order aspects of assembly and organization. Remarkably, many cytoskeletal assemblies can maintain a constant, self-organized length, even though they are nonequilibrium structures with constant molecular turnover. While significant previous work has focused on steady-state spindle length, the PI aims to advance understanding of dynamic spindle length regulation. Results from this work will provide a basis for developing predictive understanding of dynamic length regulation and cytoskeletal self-assembly.
The work is built on theoretical and modeling tools, including tractable analytic models, semi-analytic and numerical analysis, simplified simulation models, and detailed three-dimensional simulations. This project will address how length regulation and its dynamic stabilization can emerge as a collective property as the level of cytoskeletal assembly changes from single filaments, filament bundles, and the mitotic spindle. The work will focus on two scientific questions. First, what are the general mechanisms of length sensing of single cytoskeletal filaments, bundles, and higher-order assemblies? While previous length-sensing work has assumed monotonically length-dependent processes, this work will conduct a wide-ranging theoretical investigation into classes of length sensing, inspired by currently known biological processes. Second, what types of feedback and amplification lead to dynamically stable or unstable length regulation? Recent work demonstrates that mitotic spindle length is dynamically stabilized at a steady state value, and that this stabilization can be perturbed, causing large length fluctuations. The work will perform a general investigation of classes of feedback and amplification that lead to dynamically stable or unstable length of cytoskeletal assemblies. Mechanisms explored in the research may be applicable to regulating the growth of polymers and biomaterials.
The work will provide insight into biologically relevant general mechanisms of length sensing and regulation, by determining how bundling, spatially non-monotonic activity, and force-dependent regulation can effect length sensing. The work will develop understanding of the dynamic stabilization, and investigate whether there are different characteristic modes of dynamic destabilization. Research advances may have applicability to growth of biomaterials and soft materials more generally. This project will also test mechanical contributions to spindle length stabilization, by considering how spindle components contribute forces and feedback that enable constant, stable spindle length. This will improve understanding of collective self-assembly in cells. The project is an integrated interdisciplinary program of theoretical biophysics and statistical mechanics informed by cell biology and genetics to gain insight into cytoskeletal length regulation and stabilization. The PI works to increase gender and racial diversity in science through multiple activities.

This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.

PUBLICATIONS PRODUCED AS A RESULT OF THIS RESEARCH

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(Showing: 1 - 10 of 13)
Aina, Kehinde O. and Avinery, Ram and Kuan, Hui-Shun and Betterton, Meredith D. and Goodisman, Michael A. and Goldman, Daniel I. "Toward Task Capable Active Matter: Learning to Avoid Clogging in Confined Collectives via Collisions" Frontiers in Physics , v.10 , 2022 https://doi.org/10.3389/fphy.2022.735667 Citation Details
Ansari, Saad and Gergely, Zachary R. and Flynn, Patrick and Li, Gabriella and Moore, Jeffrey K. and Betterton, Meredith D. "Quantifying Yeast Microtubules and Spindles Using the Toolkit for Automated Microtubule Tracking (TAMiT)" Biomolecules , v.13 , 2023 https://doi.org/10.3390/biom13060939 Citation Details
Edelmaier, Christopher and Lamson, Adam R and Gergely, Zachary R and Ansari, Saad and Blackwell, Robert and McIntosh, J Richard and Glaser, Matthew A and Betterton, Meredith D "Mechanisms of chromosome biorientation and bipolar spindle assembly analyzed by computational modeling" eLife , v.9 , 2020 10.7554/eLife.48787 Citation Details
Fiorenza, Shane A. and Steckhahn, Daniel G. and Betterton, Meredith D. "Modeling spatiotemporally varying proteinprotein interactions in CyLaKS, the Cytoskeleton Lattice-based Kinetic Simulator" The European Physical Journal E , v.44 , 2021 https://doi.org/10.1140/epje/s10189-021-00097-8 Citation Details
Gergely, Zachary R. and Ansari, Saad and Jones, Michele H. and Zhou, Bojun and Cash, Cai and McIntosh, Richard and Betterton, Meredith D. "The kinesin-5 protein Cut7 moves bidirectionally on fission yeast spindles with activity that increases in anaphase" Journal of Cell Science , v.136 , 2023 https://doi.org/10.1242/jcs.260474 Citation Details
Lamson, Adam R. and Edelmaier, Christopher J. and Glaser, Matthew A. and Betterton, Meredith D. "Theory of Cytoskeletal Reorganization during Cross-Linker-Mediated Mitotic Spindle Assembly" Biophysical Journal , v.116 , 2019 10.1016/j.bpj.2019.03.013 Citation Details
Lamson, Adam R. and Moore, Jeffrey M. and Fang, Fang and Glaser, Matthew A. and Shelley, Michael J and Betterton, Meredith D. "Comparison of explicit and mean-field models of cytoskeletal filaments with crosslinking motors" The European Physical Journal E , v.44 , 2021 https://doi.org/10.1140/epje/s10189-021-00042-9 Citation Details
Maguire, Laura and Stefferson, Michael and Betterton, Meredith and Hough, Loren "Mechanisms of Selective Transport through the Nuclear Pore Complex" Biophysical Journal , v.114 , 2018 10.1016/j.bpj.2017.11.2375 Citation Details
Maguire, Laura D. and Betterton, Meredith E. and Hough, Loren "Bound-State Diffusion due to Binding to Flexible Polymers in a Selective Biofilter" Biophysical Journal , v.118 , 2020 10.1016/j.bpj.2019.11.026 Citation Details
Maguire, Laura D. and Stefferson, Michael E. and Betterton, Meredith and Hough, Loren "Design principles of selective transport through biopolymer barriers" Physical Review E , v.100 , 2019 10.1103/PhysRevE.100.042414 Citation Details
Moore, Jeffrey M. and Glaser, Matthew A. and Betterton, Meredith D. "Chiral self-sorting of active semiflexible filaments with intrinsic curvature" Soft Matter , 2021 https://doi.org/10.1039/D0SM01163K Citation Details
(Showing: 1 - 10 of 13)

PROJECT OUTCOMES REPORT

Disclaimer

This Project Outcomes Report for the General Public is displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed in this Report are those of the PI and do not necessarily reflect the views of the National Science Foundation; NSF has not approved or endorsed its content.

This scientific research project took inspiration from cell division and biological filtering to better understand the biophysics that drives these processes. The project gave key results on bipolar spindle assembly. During cell division, a structure known as the mitotic spindle is crucial for proper chromosome segregation. Surprisingly, the project showed that molecular motors, usually essential for spindle assembly, were not always required. By utilizing molecular simulations and a minimal torque-balance model, they successfully predicted spindle length even in the absence of these motors. This finding opens up further research into the underlying mechanisms that drive spindle assembly. The project then developed a new theory of mitotic spindle assembly and chromosome alignment. The simulations they created not only provided fresh insights into spindle length regulation but also error correction during chromosome alignment. They also analyzed the mechanisms that contribute to spindle length fluctuations, important for how cells divide and ensure their genetic material is accurately distributed. Spindle stability depends on the regulation of microtubule antiparallel overlaps. The project developed novel theory and simulations for this system, which led to new work identifying intriguing long-range interactions between molecular motors mediated by microtubules. The project also established new results on selective transport and filtering through biopolymer barriers. The project discovered that binding and unbinding from flexible polymers could lead to selective transport. This contributes to our understanding of nucleocytoplasmic transport in cells. The project developed new simulation tools to study filaments that are driven by motors and interact, producing several software packages for use by the community.  This research project has impacted on several scientific disciplines, including statistical physics, cell biology, biophysics, and computational physics. The work on spindle self-assembly and chromosome segregation has improved our understanding of cell division, a process fundamental to cellular life. The project has contributed to training the next generation of researchers. Undergraduate and graduate students have been mentored in this project. In conclusion, the outcomes of this project have brought us closer to understanding the cell division and the selective transport in cells.


Last Modified: 08/01/2023
Modified by: Meredith D Betterton

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