Graphical abstract
Many methods exist for quantifying cellular traction forces, including traction force microscopy and microfabricated post arrays. However, these methodologies have limitations, including a requirement to remove cells to determine undeflected particle locations and the inability to quantify forces of cells with low cytoskeletal stiffness, respectively. Here we present a novel method of traction force quantification that eliminates both of these limitations. Through the use of a hexagonal pattern of microcontact-printed protein spots, a novel computational algorithm, and thin surfaces of polydimethyl siloxane (PDMS) blends, we demonstrate a system that: • quantifies cellular forces on a homogeneous surface that is stable and easily manufactured. • utilizes hexagonal patterns of protein spots and computational geometry to quantify cellular forces without need for cell removal. • quantifies cellular forces in cells with low cytoskeletal rigidity.