Paul MATSUDAIRA
Founding Deputy Director and Professor, Mechanobiology Institute, National University of Singapore
Research Program
Leader, Mechanotransduction in Tissues
Affiliations
Emeritus Professor, Department of Biological Sciences, National University of Singapore
Emeritus Professor, Centre for BioImaging Sciences, Department of Biological Sciences, National University of Singapore
EASMB Symposium 2025 Showcases Global Participation and Relevance
The East Asian Single-Molecule Biophysics Symposium 2025 (EASMB2025) held from 24 to 26 November at the Ngee Ann Kongsi Auditorium in the Education Resource Centre, UTown, National University of Singapore showcased global participation and relevance.
Ng Inn Chuan
Research Associate, Yu Group
Byun Young Seo Christina
Research Assistant, Tee Group
Paul Matsudaira
Emeritus Professor
Research Areas
Mechanobiology of cells and tissues on viscoelastic surfaces, nanoscale dynamics, biomaging sciences.
Research Interests
The Matsudaira Lab studies the role of mechanics in epithelial tissue migration and remodeling during development and disease. The organization and migration of epithelial tissues are sensitive to the underlying substratum, especially on visco-elastic substrates. This range of stiffness defines the environment of most basement membranes, cell-cell interactions, and early developmental processes. On the one hand, the lab is interested in the mechanical signatures of the development of chirality, convergence, and extension during the early steps in morphogenesis of the Zebrafish embryo. Other studies are focused on the role of substrate viscoelasticity in tissue remodeling during disease and its regulation by cell-matrix and cell-cell signaling pathways. In order to study complex, multi-scale dynamics the lab develops and applies novel imaging methods such as in situ TEM and strain light-sheet microscopy.
Biography
Formerly a biology and bioengineering professor at the Massachusetts Institute of Technology (MIT), Paul Matsudaira has studied the cytoskeleton since graduating from college. He was the EM technician of Tom Schroeder where he helped investigate the role of microfilaments in the contractile ring. As a graduate student of Dave Burgess he identified the structure and function of the intestine brush border cytoskeleton. Following postdoctoral research on the assembly of actin bundles at the MPI Biophysical Chemistry with Klaus Weber and the MRC LMB with Alan Weeds, Paul started his academic career at the Whitehead Institute and MIT where his lab studied biophysics of actin and other polymer protein bundles, mechanics of polymers and single cells motility, and developed microanalytical methods. In 2009, he moved to Singapore to establish the Centre for BioImaging Sciences, head the Department of Biological Sciences, and help found the Mechanobiology Institute, National University of Singapore.
Education
PhD in Biological Sciences from Dartmouth College, Hanover, New Hampshire
Selected Publications (5 of 177)
- Zheng J, Han SP, Chiu YJ, Yip AK, Boichat N, Pauli AR, Zhu S, Matsudaira P. 2017 Substrate viscoelasticity induces coalescence of epithelial monolayers via subcellular redistribution of vinculin. Biophys J. 113:1585-98.
- Loh D, Sen S, Bosman M, Tan SF, Zhong J, Nijhuis C, Kral P, Matsudaira P, Mirsaidov U. 2016 Multi-step nucleation of nanocrystals in aqueous solution. Nat. Chem 9:77-82.
- Ai Kia Yip, Keng-Hwee Chiam and Paul Matsudaira. Traction stress analysis and modeling reveal that amoeboid migration in confined spaces is accompanied by expansive forces and requires the structural integrity of the membrane–cortex interactions. Integrative Biology, 2015, DOI: 10.1039/ C4IB00245H. First published online 27 May 2015
- Bhattacharya D, Singh V R, Zhi C, Peter T C, Matsudaira P, Barbastathis G. 2012. Three dimensional HiLo-based structured illumination for a Digital Scanned Laser Sheet Microscopy (DSLM) in thick tissue imaging. Optics Express 20(25):27337-27347.
- Mirsaidov UM, Zheng H, Bhattacharya D, Casana Y, Matsudaira P. 2012. Imaging protein structure in water at 2.7 nm resolution by TEM. Biophys J. 102:L15-7.
Recent Publications
- Zhu S, Loo YT, Veerapathiran S, Loo TYJ, Tran BN, Teh C, Zhong J, Matsudaira P, Saunders TE, and Wohland T. Receptor binding and tortuosity explain morphogen local-to-global diffusion coefficient transition. Biophys J 2024;. [PMID: 39049492]
- Tavakoli S, Zhu S, and Matsudaira P. Cell clusters containing intestinal stem cells line, the zebrafish intestine intervillus pocket. iScience 2022; 25(5):104280. [PMID: 35586068]
- Bhattacharya D, Zhong J, Tavakoli S, Kabla A, and Matsudaira P. Strain maps characterize the symmetry of convergence and extension patterns during zebrafish gastrulation. Sci Rep 2021; 11(1):19357. [PMID: 34588480]
- Wu H, Ng DTW, Cheong I, and Matsudaira P. The degradation-promoting roles of deubiquitinases Ubp6 and Ubp3 in cytosolic and ER protein quality control. PLoS ONE 2020; 15(5):e0232755. [PMID: 32401766]
- Chan SN, Prasad R, and Matsudaira P. Genetic Selection Based on a Ste6*C-HA-Ura3 Substrate Identifies New Cytosolic Quality Control Alleles in Saccharomyces cerevisiae. G3 (Bethesda) 2020; 10(6):1879-1891. [PMID: 32299823]
- Matsudaira PT, and Verma CS. Editorial. Prog. Biophys. Mol. Biol. 2019;. [PMID: 30951764]
- Wadduwage DN, Singh VR, Choi H, Yaqoob Z, Heemskerk H, Matsudaira P, and So PTC. Near-common-path interferometer for imaging Fourier-transform spectroscopy in wide-field microscopy. Optica 2017; 4(5):546-556. [PMID: 29392168]
- Zheng JY, Han SP, Chiu Y, Yip AK, Boichat N, Zhu SW, Zhong J, and Matsudaira P. Epithelial Monolayers Coalesce on a Viscoelastic Substrate through Redistribution of Vinculin. Biophys. J. 2017;. [PMID: 28844472]
- Zheng JY, Tan HL, Matsudaira PT, and Choo A. Excess reactive oxygen species production mediates monoclonal antibody-induced human embryonic stem cell death via oncosis. Cell Death Differ. 2017;. [PMID: 28106884]
- . https://www.ncbi.nlm.nih.gov/pubmed/28007915
MBI Lab Members
What are intermediate filaments?
What are intermediate filaments? Intermediate filaments are a primary component of the cytoskeleton, although they are not found in all eukaryotes, and are absent in fungi and plants [1]. These filaments, which extend throughout [...]
How are intermediate filaments assembled?
How are intermediate filaments assembled? The soluble subunit for creating intermediate filaments is a tetramer. The tetramer is created from monomers in a stepwise fashion (as reviewed in [1]). First, two monomers associate via [...]
What are microtubules?
What are microtubules? Microtubules are hollow cylinders [1] that are approximately 25nm in diameter [2] and vary in length from 200 nm to 25 μm. They are formed by the lateral association of between [...]
How does the tubulin complex assemble?
How does the tubulin complex assemble? Microtubules are made up of repeating units of α/β- tubulin heterodimers, which are assembled on a γ-tubulin ring complex (a complex of γ-tubulin and other protein components), during [...]
How is microtubule assembly/disassembly regulated?
How is microtubule assembly/disassembly regulated? GTP hydrolysis has been shown to be a key regulator of microtubule polymerization dynamics. Although the exact mechanisms are poorly understood, two opposing models have been proposed to describe [...]
What is microtubule dynamic instability?
What is microtubule dynamic instability? In most cell types, thirteen protofilaments associate laterally to form a microtubule. In a few cases microtubules contain more or fewer protofilaments [1]. Numerous interactions between the subunits give [...]
What is the role of microtubules in mechanotransduction?
What is the role of microtubules in mechanotransduction? Microtubules exist in all cells, however their influence in the mechanotransduction of mechanical stimuli has been described at length in cardiac striated muscle [1]. Mechanical stimuli [...]
What are Contractile Fibers?
What are Contractile Fibers? Certain myosin isoforms (i.e. myosin II) form bipolar assemblies via the extended coiled-coil domains in the heavy chains (see also “thick filaments”). Actin “thin filaments” with opposite polarity associate with [...]
How is actomoysin contractility regulated?
How does the contractome protein network regulate actomyosin contractility? Non-muscle myosin II isoforms have a similar structure and function to their muscle equivalents. However, their interaction with actin serves to generate cellular forces rather [...]
What are Blebs?
What are Blebs? Blebs are blister-like protrusions that occur at the cell surface (reviewed in [1]). Blebs form, and function, in a series of defined steps. They typically grow to a length of around [...]
What is Actomyosin?
What is Actomyosin? Actomyosin refers to the actin-myosin complex that forms within the cytoskeleton. Actomyosin is inherently contractile, with the myosin motor protein able to pull on actin filaments. This property gives rise to [...]
How do filopodia move dynamically?
What causes filopodia retraction and collapse? Binding of filopodia to certain ligands or substratum may hinder filament assembly, thereby leading to changes that promote retraction, collapse or growth cone turning [1][2]. For example, substrate [...]
