Michael SheetzManagement2020-08-12T10:33:48+08:00
Michael SHEETZ

Michael SHEETZ

Founding Director and Collaborator, Mechanobiology Institute, National University of Singapore

misheetz@utmb.edu

Affiliations
Professor, Department of Biochemistry & Molecular Biology, UTMB Health

What is phagocytosis?

What is phagocytosis? Phagocytosis is a process by which cells ingest large particles (> 0.5 micrometers) into membrane-bound vesicles called phagosomes, which are then targeted to the lysosomes for enzymatic degradation. The internalization of [...]

By Management|Nov 30th, 2023|Categories: MBInfo, Membrane Dynamics|Comments Off on What is phagocytosis?

Genome Regulation

Genome Regulation Genome regulation encompasses all facets of gene expression, from the biochemical modifications of DNA, to the physical arrangement of chromosomes and the activity of the transcription machinery. The genome regulation programs that [...]

By Management|Nov 30th, 2023|Categories: Genome Regulation, MBInfo|Comments Off on Genome Regulation

What is caveolar endocytosis?

What is caveolar endocytosis? Macropinocytosis or ‘cell drinking’ is a type of endocytosis that involves the nonspecific uptake of extracellular material, such as soluble molecules, nutrients, and antigens. First observed in 1931 by Warren [...]

By Management|Nov 30th, 2023|Categories: MBInfo, Membrane Dynamics|Comments Off on What is caveolar endocytosis?

What are chromosomes and chromosome territories?

What are chromosomes and chromosome territories? While metaphase chromosomes can be depicted as distinct bodies with well-defined shapes and sizes, interphase chromosomes are less uniform and, by filling the nuclear space, difficult to distinguish. [...]

By Management|Nov 30th, 2023|Categories: Genome Regulation, MBInfo|Comments Off on What are chromosomes and chromosome territories?

How does the nucleus facilitate mechanotransduction?

What properties of the nucleus facilitate mechanotransduction? Similar to the concept of long distance force propagation along the cytoskeleton, the prestressed nuclear state, which counterbalances intracellular forces from the cytoskeleton, enables mechanotransduction [1][2]. Both [...]

By Management|Nov 30th, 2023|Categories: Genome Regulation, MBInfo|Comments Off on How does the nucleus facilitate mechanotransduction?

Michael Sheetz

Collaborator

Research Areas

Cell migration, cell-cell and cell-substrate interaction

Research Interests

The morphology of cells, organs and whole organisms is determined by the generation of forces on the immediate environment, which is either extracellular matrix or adjacent cells. We are currently engaged in studies to understand the detailed molecular mechanisms involved in a variety of phenomena from cancer metastasis to brain function. Further, we are developing several new tools and protocols for measuring cell forces at the molecular level, which are revealing many new aspects of how cells can both generate and respond to external forces. We have an effort underway to define quantitatively the steps involved in cell adhesion to and spreading on a matrix-coated surface. Using a variety of cell lines that are missing proteins in various motility pathways, we are determining the quantitative changes in the spreading process. This will enable us to generate a detailed model of the process of spreading that will be a model for further studies of how cells differentiate, regenerate tissues or metastasize.

Biography

Hailing from Columbia University, Prof Michael Sheetz has more than 40 years’ experience in the biomedical field. Introduced to Singapore by Prof Hew Choy Leong of the National University of Singapore’s Department of Biological Sciences, Prof Sheetz was sought to lead an RCE project. This resulted in a two-year effort to organise and submit a proposal on Mechanobiology where Prof Sheetz set the theme and direction of the Mechanobiology Institute (MBI). As Founding Director of the MBI, he led the institute for 10 years and built it into a world-leading research centre in the field of mechanobiology.

Education

PhD California Institute of Technology

Recent Publications

  1. Jain K, Kishan K, Minhaj RF, Kanchanawong P, Sheetz MP, and Changede R. Immobile Integrin Signaling Transit and Relay Nodes Organize Mechanosignaling through Force-Dependent Phosphorylation in Focal Adhesions. ACS Nano 2025;. [PMID: 39760672]
  2. Lin S, Changede R, Farrugia AJ, Bershadsky AD, Sheetz MP, Prost J, and Rupprecht J. Membrane Tilt Drives Phase Separation of Adhesion Receptors. Phys Rev Lett 2024; 132(18):188402. [PMID: 38759206]
  3. Jain K, Minhaj RF, Kanchanawong P, Sheetz MP, and Changede R. Nano-clusters of ligand-activated integrins organize immobile, signalling active, nano-clusters of phosphorylated FAK required for mechanosignaling in focal adhesions. bioRxiv 2024;. [PMID: 38464288]
  4. Jain K, Pandey A, Wang H, Chung T, Nemati A, Kanchanawong P, Sheetz MP, Cai H, and Changede R. TiO2 Nano-Biopatterning Reveals Optimal Ligand Presentation for Cell-Matrix Adhesion Formation. Adv Mater 2024;:e2309284. [PMID: 38340044]
  5. Jain K, Lim KYE, Sheetz MP, Kanchanawong P, and Changede R. Intrinsic self-organization of integrin nanoclusters within focal adhesions is required for cellular mechanotransduction. bioRxiv 2023;. [PMID: 38045378]
  6. Oh D, Liu X, Sheetz MP, and Kenney LJ. Small, Dynamic Clusters of Tir-Intimin Seed Actin Polymerization. Small 2023;:e2302580. [PMID: 37649226]
  7. Qin R, Melamed S, Yang B, Saxena M, Sheetz MP, and Wolfenson H. Tumor Suppressor DAPK1 Catalyzes Adhesion Assembly on Rigid but Anoikis on Soft Matrices. Front Cell Dev Biol 2022; 10:959521. [PMID: 35927990]
  8. Jain K, Kanchanawong P, Sheetz MP, Zhou X, Cai H, and Changede R. Ligand functionalization of titanium nanopattern enables the analysis of cell-ligand interactions by super-resolution microscopy. Nat Protoc 2022;. [PMID: 35896742]
  9. Toh PJY, Lai JKH, Hermann A, Destaing O, Sheetz MP, Sudol M, and Saunders TE. Optogenetic control of YAP cellular localisation and function. EMBO Rep 2022;:e54401. [PMID: 35876586]
  10. Oh D, Chen Z, Biswas KH, Bai F, Ong HT, Sheetz MP, and Groves JT. Competition for shared downstream signaling molecules establishes indirect negative feedback between EGFR and EphA2. Biophys J 2022;. [PMID: 35430415]

Lab Members

Yow Ying Ming Ivan

May 16th, 2017|Comments Off on Yow Ying Ming Ivan

Schimdt AI in Science Postdoctoral Fellow, Low Group

Saw Thuan Beng

Apr 25th, 2017|Comments Off on Saw Thuan Beng

Alumni, Research Assoicate, Lim Group, Ladoux Group

Le Anh Phuong

Apr 25th, 2017|Comments Off on Le Anh Phuong

Alumni, Research Assistant, Toyama Group

Sivakumar s/o Maniam

Apr 25th, 2017|Comments Off on Sivakumar s/o Maniam

Alumni, Research Associate, Grenci Group

So-SPIM-FCS

Apr 21st, 2017|Comments Off on So-SPIM-FCS

A novel tool for imaging nuclear protein dynamics

Signaling in 3D

Apr 21st, 2017|Comments Off on Signaling in 3D

MBI Scientists reveal a spatial dimension to cell signaling

From the Bottom Up

Apr 20th, 2017|Comments Off on From the Bottom Up

Basal protrusions stimulate rosette formation during cell intercalation

B(a)iled Out

Apr 20th, 2017|Comments Off on B(a)iled Out

Actin remodeling drives bile regurgitation during obstructive cholestasis

Minnah Thomas

Apr 20th, 2017|Comments Off on Minnah Thomas

Alumni, Toyama Group

Murat Shagirov

Apr 20th, 2017|Comments Off on Murat Shagirov

Research Fellow (HPC), IT Core

Yusuke Hara

Apr 20th, 2017|Comments Off on Yusuke Hara

Alumni, Toyama Group

Lim Kok Hwee Isaac

Apr 20th, 2017|Comments Off on Lim Kok Hwee Isaac

Research Assistant, Toyama Group

About the National University of Singapore

About NUSA leading global university centred in Asia, NUS is Singapore's flagship university, offering a global approach to education and research with a focus on Asian perspectives and expertise.

About the Mechanobiology Institute, National University of Singapore

About MBIOne of four Research Centres of Excellence at NUS, MBI is working to identify, measure and describe how the forces for motility and morphogenesis are expressed at the molecular, cellular and tissue level.
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