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April 22, 2026Current Opinion in Chemical Biology0 citationsOpen Access

Proximity labeling tools for studying chromatin interactomes

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FTFeifei TongCSCiaran P. Seath

Key Points

  • This paper aims to examine the advancements in proximity labeling technologies for studying chromatin interactomes.
  • Review protein-centered and nucleic-acid-centered proximity labeling approaches.
  • Discuss nanoscale and mesoscale photocatalytic systems, genetically encoded modalities, and CRISPR guidance.
  • Highlight the use of structure-specific sensors for mapping diverse RNA species.
  • Proximity labeling technologies enhance the resolution of chromatin interaction studies.
  • They allow for the characterization of histone-associated interaction networks and PTM-dependent microenvironments.
  • New strategies have broadened the utility of these tools, facilitating research across various aspects of chromatin biology.

Abstract

Studying protein and nucleic acid interactions within chromatin remains challenging, as these events occur in a densely packed and dynamic nuclear environment. Proximity labeling technologies now offer powerful solutions by enabling spatially and temporally resolved characterization of chromatin microenvironments in living cells. Recent advances in labeling chemistry, photocatalytic platforms, and targeting strategies have improved precision and efficiency, broadening their utility across chromatin biology. Here, we review protein-centered proximity labeling approaches-including nanoscale and mesoscale photocatalytic systems, genetically encoded modalities, and antibody-directed labeling-that reveal histone-associated interaction networks and PTM-dependent microenvironments. We also highlight nucleic-acid-centered platforms that use CRISPR guidance, hybridization-based targeting, or structure-specific sensors to map protein complexes at defined genomic loci, diverse RNA species, and noncanonical structures such as G-quadruplexes and R-loops. Together, these technologies are reshaping how chromatin interactomes are measured. We conclude by outlining key challenges and future opportunities that will guide next-generation proximity labeling tools for chromatin research.

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Cite This Study

Tong et al. (2026) studied this question.

synapsesocial.com/papers/69e864866e0dea528dde945chttps://doi.org/10.1016/j.cbpa.2026.102686
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