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A novel method for quantifying traction forces on hexagonal micropatterned protein features on deformable poly-dimethyl siloxane sheets

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...

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Detalles Bibliográficos
Autores principales: Griffin, Brian P., Largaespada, Christopher J., Rinaldi, Nicole A., Lemmon, Christopher A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6690417/
https://www.ncbi.nlm.nih.gov/pubmed/31417850
http://dx.doi.org/10.1016/j.mex.2019.05.011
Descripción
Sumario: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.