PIPages
Labs

Douglas N Robinson

Johns Hopkins University, MD·Biophysics

Cells constantly push, pull and get squeezed, and they must sense these forces to divide, move, grow and build tissues. Inside the cell, a protein scaffolding called the cytoskeleton assembles where force is applied and then comes apart again.

Fields

Biophysics

Biology

Biochemistry

Topics

mechanobiology

cytoskeleton

mechanosensing

Grants
1 known grant, through Feb 2027

What they work on

  1. Test SpringSaLaD computer-model predictions about how Contractility Kits, premade bundles of myosin II, cortexillin I and IQGAP proteins, form in Dictyostelium amoebae, using measured cellular concentrations and binding strengths.
  2. Determine how mechanical force drives the assembly of Contractility Kits and nonmuscle myosin II bipolar thick filaments, using interference scattering mass spectrometry to weigh single molecules and complexes.
  3. Measure the stretchiness of myosin thick filaments with magnetic tweezers and test how it limits the disassembling enzymes MHCKC (in Dictyostelium) and PKCzeta (for human NMIIB).
  4. Determine how the roughly 20% assembly setpoint of myosin's force-driven accumulation, which differs by cell type and cell-cycle stage, shapes NMIIB dynamics, cell division and gene expression.

More about the research

Because the machinery assembles in response to force, it can tune itself, and it can turn a physical input into a chemical signal. How this force-guided assembly works at the molecular level, and how it changes what a cell does, is the central question of this work.

Why it matters

Force sensing is needed for cells to multiply, for normal development and for keeping the body healthy. By showing how mechanical forces guide the local assembly of myosin II and related machinery, and how this shifts cell behavior and identity, the work could inform understanding of how cells divide and change fate. It also offers a modeling framework that others can apply to force-responsive protein systems.

Known grants

From NIH and NSF research grants. Labs often have other funding we can't see.

Molecular Mechanisms of Cytoskeletal Mechanosensory Systems

NIH · Apr 2023 – Feb 2027

Closest labs

E. Ostap

University of Pennsylvania, PA·Biophysics

Determine the structural basis of myosin force sensing by testing conserved residues that tune tension sensitivity in Myo1b and Myo1c, using engineered motors, microsecond optical trapping and cryo-EM.

Dimitrios Vavylonis

Lehigh University, PA·Biophysics

Model how fission yeast nodes — membrane protein clusters that time cell cycle progression and cytokinesis — assemble at the nanoscale, focusing on interactions of Cdc15, Mid1 and Cdr2 with each other and with the membrane.

Gregory Alushin

Rockefeller University, NY·Biophysics

Determine the structural mechanisms and cellular functions of catch bonds, protein contacts that strengthen under pulling force, in cytoskeletal crosslinking proteins and cell adhesion proteins implicated in force sensing.

The school

Johns Hopkins University: 100 labs on PI Pages, $4.1B a year on research, 622 research doctorates a year.

More about Johns Hopkins University

Reach out

A start for your email. Fill in the brackets.