@article{22403,
  abstract     = {Linear phase‐contrast scanning transmission electron microscopy (STEM) techniques compatible with high‐throughput 4D‐STEM acquisition are widely used to enhance phase contrast in weakly scattering and beam‐sensitive materials. In these modalities, contrast transfer is often suppressed at low spatial frequencies, resulting in a characteristic contrast gap that limits contrast. Approaches that retain low‐frequency phase contrast exist but typically require substantially increased experimental complexity, restricting routine use. Dark‐field STEM imaging captures this missing low‐frequency information through electrons scattered outside the bright‐field disk, but discards a large fraction of the scattered signal and is therefore dose‐inefficient. Fused Full‐field STEM (FF‐STEM) is introduced as a 4D‐STEM imaging modality that overcomes these limitations by combining ptychographic phase reconstruction with tilt‐corrected dark‐field imaging within a single acquisition. Bright‐field data are used to estimate probe aberrations and reconstruct a high‐resolution phase image, while dark‐field data provide complementary low‐frequency contrast. The two channels are fused in Fourier space using Wiener‐band weighting based on the spectral signal‐to‐noise ratio, yielding transfer‐gap‐free images with high contrast. FF‐STEM preserves the upsampling and depth‐sectioning capabilities of ptychography, adds robust low‐frequency contrast characteristic of dark‐field imaging, and enables dose‐efficient, near–real‐time reconstruction.},
  author       = {You, Shengbo and Varnavides, Georgios and Khavnekar, Sagar and Palatkin, Nikita and Shao, Sihan and Wu, Mingjian and Stroppa, Daniel and Chernikova, Darya and Zhu, Baixu and Egoavil, Ricardo and Vespucci, Stefano and Krishnan, Dileep and Ye, Xingchen and Schur, Florian KM and Spiecker, Erdmann and Pelz, Philipp},
  issn         = {2198-3844},
  journal      = {Advanced Science},
  publisher    = {Wiley},
  title        = {{Gap‐free information transfer in 4D‐STEM via fusion of complementary scattering channels}},
  doi          = {10.1002/advs.76620},
  year         = {2026},
}

@article{17884,
  abstract     = {Human T cell leukemia virus type 1 (HTLV-1) immature particles differ in morphology from other retroviruses, suggesting a distinct way of assembly. Here we report the results of cryo-electron tomography studies of HTLV-1 virus-like particles assembled in vitro, as well as derived from cells. This work shows that HTLV-1 uses a distinct mechanism of Gag–Gag interactions to form the immature viral lattice. Analysis of high-resolution structural information from immature capsid (CA) tubular arrays reveals that the primary stabilizing component in HTLV-1 is the N-terminal domain of CA. Mutagenesis analysis supports this observation. This distinguishes HTLV-1 from other retroviruses, in which the stabilization is provided primarily by the C-terminal domain of CA. These results provide structural details of the quaternary arrangement of Gag for an immature deltaretrovirus and this helps explain why HTLV-1 particles are morphologically distinct.},
  author       = {Obr, Martin and Percipalle, Mathias and Chernikova, Darya and Yang, Huixin and Thader, Andreas and Pinke, Gergely and Porley, Dario J and Mansky, Louis M. and Dick, Robert A. and Schur, Florian KM},
  issn         = {1545-9985},
  journal      = {Nature Structural & Molecular Biology},
  pages        = {268--276},
  publisher    = {Springer Nature},
  title        = {{Distinct stabilization of the human T cell leukemia virus type 1 immature Gag lattice}},
  doi          = {10.1038/s41594-024-01390-8},
  volume       = {32},
  year         = {2025},
}