@article{202251,
  keywords = {Fibril, Fibrillogenesis, Fibronectin, Live imaging, Super-resolution microscopy},
  author = {Darshika Tomer and Cecilia Arriagada and Sudipto Munshi and Brianna Alexander and Brenda French and Pavan Vedula and Valentina Caorsi and Andrew House and Murat Guvendiren and Anna Kashina and Jean Schwarzbauer and Sophie Astrof},
  title = {A new mechanism of fibronectin fibril assembly revealed by live imaging and super-resolution microscopy.},
  abstract = {<p>Fibronectin (Fn1) fibrils have long been viewed as continuous fibers composed of extended, periodically aligned Fn1 molecules. However, our live-imaging and single-molecule localization microscopy data are inconsistent with this traditional view and show that Fn1 fibrils are composed of roughly spherical nanodomains containing six to eleven Fn1 dimers. As they move toward the cell center, Fn1 nanodomains become organized into linear arrays, in which nanodomains are spaced with an average periodicity of 105{\textpm}17 nm. Periodical Fn1 nanodomain arrays can be visualized between cells in culture and within tissues; they are resistant to deoxycholate treatment and retain nanodomain periodicity in the absence of cells. The nanodomain periodicity in fibrils remained constant when probed with antibodies recognizing distinct Fn1 epitopes or combinations of antibodies recognizing epitopes spanning the length of Fn1. Treatment with FUD, a peptide that binds the Fn1 N-terminus and disrupts Fn1 fibrillogenesis, blocked the organization of Fn1 nanodomains into periodical arrays. These studies establish a new paradigm of Fn1 fibrillogenesis. This article has an associated First Person interview with the first author of the paper.</p>
},
  year = {2022},
  journal = {Journal of cell science},
  volume = {135},
  month = {08/2022},
  issn = {1477-9137},
  doi = {10.1242/jcs.260120},
  language = {eng},
}