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          <dc:title>Nanometer-resolution imaging of living bacteria across species and cellular orientations</dc:title>
          <dc:creator>Anna Scheeder (20969870)</dc:creator>
          <dc:creator>Joanna Szczepaniak (24696002)</dc:creator>
          <dc:creator>Yulianna (Julie) Koziy (17035479)</dc:creator>
          <dc:creator>Naomi Mara Claro De Oliveira (19764864)</dc:creator>
          <dc:creator>Will Trewby (17726106)</dc:creator>
          <dc:creator>Renata Kaminska (24696007)</dc:creator>
          <dc:creator>Jeremy Brown (6778883)</dc:creator>
          <dc:creator>Colin Kleanthous (11361259)</dc:creator>
          <dc:creator>Bart Hoogenboom (6781322)</dc:creator>
          <dc:subject>Bacteriology</dc:subject>
          <dc:subject>Soft condensed matter</dc:subject>
          <dc:subject>Biological physics</dc:subject>
          <dc:subject>Receptors and membrane biology</dc:subject>
          <dc:subject>Cellular interactions (incl. adhesion, matrix, cell wall)</dc:subject>
          <dc:subject>Structural biology (incl. macromolecular modelling)</dc:subject>
          <dc:subject>Atomic force microscopy</dc:subject>
          <dc:subject>Bacterial cell envelopes</dc:subject>
          <dc:subject>Bacterial surfaces</dc:subject>
          <dc:subject>Biological membranes</dc:subject>
          <dc:subject>Outer membrane</dc:subject>
          <dc:subject>Supramolecular structure</dc:subject>
          <dc:subject>Imaging</dc:subject>
          <dc:description>&lt;p dir="ltr"&gt;The bacterial cell envelope is a complex superstructure that is an important target and a major barrier for antibiotics. To date, highest-resolution images of native cell envelopes have been obtained by atomic force microscopy (AFM), but its use is limited by challenges in bacterial immobilization. We establish glutaraldehyde-functionalized glass surfaces for reversible covalent attachment, enabling robust adhesion across species and cellular orientations while preserving cell viability and growth. This approach allowed imaging of &lt;i&gt;Escherichia coli&lt;/i&gt; both expressing O-antigen and fully lacking lipopolysaccharide (LPS) oligosaccharides, revealing that AFM contrast depends on LPS complexity and confirming previously observed outer membrane domains as LPS-enriched islands. It also enabled imaging of &lt;i&gt;Pseudomonas aeruginosa&lt;/i&gt; and &lt;i&gt;Acinetobacter baumannii&lt;/i&gt; outer membranes, which lack the characteristic protein trimers observed in model &lt;i&gt;E. coli&lt;/i&gt;. Finally, we discovered growth-phase dependent alterations in &lt;i&gt;E. coli&lt;/i&gt; pole morphology, where trimer networks typical of exponential-phase cells were unresolved and morphological defects appeared.&lt;/p&gt;&lt;p dir="ltr"&gt;This data set contains the source data for a publication on the study as described above, which has been accepted-in-principle for publication at &lt;i&gt;Nature Communication&lt;/i&gt; (2026). The data is in the form of numeric tables, images and microscopy source data that can al be accessed by open-source software.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-15T12:51:49Z</dc:date>
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          <dc:type>Dataset</dc:type>
          <dc:identifier>10.5522/04/33416257.v1</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Nanometer-resolution_imaging_of_living_bacteria_across_species_and_cellular_orientations/33416257</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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