Abstract

The nano-scale structure of cytoskeletal biopolymers as well as sophisticated superstructures determine the versatile cellular shapes and specific mechanical properties. One example is keratin intermediate filaments in epithelial cells, which form thick bundles that can further organize in a cross-linked network. To study the native structure of keratin bundles in whole cells, high-resolution techniques are required, which do at the same time achieve high penetration depths. We employ scanning x-ray diffraction using a nano-focused x-ray beam to study the structure of keratin in freeze-dried eukaryotic cells. By scanning the sample through the beam we obtain x-ray dark-field images with a resolution of the order of the beam size, which clearly show the keratin network. Each individual diffraction pattern is further analyzed to yield insight into the local sample structure, which allows us to determine the local structure orientation. Due to the small beam size we access the structure in a small sample volume without performing the ensemble average over one complete cell.

Highlights

  • The nano-scale structure of cytoskeletal biopolymers as well as sophisticated superstructures determine the versatile cellular shapes and specific mechanical properties

  • A diffraction pattern is recorded and can further be analyzed to yield structural information averaged over the probed sample volume

  • Diffraction patterns in reciprocal space are analyzed with respect to signal orientation and anisotropy, which allows us to determine the local structure orientation in the sample

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Summary

Introduction

The nano-scale structure of cytoskeletal biopolymers as well as sophisticated superstructures determine the versatile cellular shapes and specific mechanical properties. The step toward the use of a sub-micron beam reduces the probed sample volumes to dimensions, which allow to investigate structural properties of nano-scale objects without averaging over a large ensemble [27]. We present scanning diffraction experiments using a nano-focused x-ray beam with a focal spot size of about 150 × 150 nm on freeze-dried cells, which are transfected with genes encoding for keratins K8 and K18. In these cells, keratin filaments form bundles and organize in a cross-linked network. Diffraction patterns in reciprocal space are analyzed with respect to signal orientation and anisotropy, which allows us to determine the local structure orientation in the sample

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