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Volume 657 Issue 8130, 3 September 2026
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Volume 657 Issue 8130, 3 September 2026

Chemical microscopy

Fluorescence microscopy has enabled high-resolution images to be captured of molecular processes in live cells, but the need for an external light source can cause issues. An alternative approach is to use luminescence that is generated as the result of a chemical reaction, thereby avoiding the need for a light source, but this approach suffers from limited resolution. In this week’s issue, Jiandong Feng and colleagues address this problem with a chemistry-based super-resolution imaging framework that can achieve 3D, laser-free, high-sensitivity and long-term imaging in live cells. The researchers have tested their process in systems using electrochemiluminescence, chemiluminescence and bioluminescence and for each managed to derive an image of much higher resolution than was previously possible. The cover shows one such image, captured by applying the framework to chemiluminescent imaging of a 3D microtubule network in darkness.

Cover image: Wenxin Zhu/Jiahui Gui/Weisong Zhao/Jiandong Feng.

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      Article Open Access
    • Local Lewis-base hardness is tuned through a molecular dipole, an approach constraining the polarizability of the oxygen donor’s outermost electrons, leading to homogeneous WBG films achieving enhanced power conversion efficiency and extended stability.

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    • A new chemistry-based super-resolution imaging framework is described, enabling 3D, laser-free, highly sensitive and ultralong-term imaging of live cells which overcomes the limitations in spatiotemporal resolution associated with reaction-based imaging methods.

      • Wenxin Zhu
      • Chi Zhang
      • Jiandong Feng
      Article Open Access
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      • Matthew Gibson
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    • An encyclopedia of more than 92 million enhancer–gene regulatory interactions created as part of the ENCODE4 project provides a valuable resource for future studies of gene regulation and human genetics.

      • Andreas R. Gschwind
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    • Single-nucleus RNA-seq and ATAC-seq analyses on post-mortem brain samples from African American, Latin and white individuals identify cell-type-specific molecular signatures that are associated with cognitive impairment and/or Alzheimer’s disease across diverse population groups.

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    • Epitope editing of KIT enables antibody-based, non-genotoxic conditioning that selectively enriches therapeutic BCL11A-edited haematopoietic stem/progenitor cells, supports durable engraftment, preserves clonal diversity and enhances induction of fetal haemoglobin, a therapeutic approach for conditions such as sickle cell disease and β-thalassemia.

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