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Volume 43 Issue 2, February 2025

Designing drugs with reversible activity

Illustration from a crystal structure of the coagulation factor thrombin inhibited by two drug–peptide nucleic acid (PNA) molecules (pink and purple) bound together by base pairing; a PNA antidote (green) can release the inhibitor through competitive binding. Dockerill et al. describe a PNA-based approach to creating drugs with on-demand reversibility.

See Dockerill et al.

Image: Kate Zvorykina and Ella Marushchenko (Ella Maru Studio). Cover design: Erin Dewalt

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  • Ultrasound neurotechnologies are moving quickly into clinical trials in a wide variety of applications, and initiatives to open-source their manufacture will make them more accessible.

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    • Recent patents relating to antibody compositions and methods of use.

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  • Cells interact with their local environment to enact global tissue function. By harnessing gene–gene covariation in cellular neighborhoods from spatial transcriptomics data, the covariance environment (COVET) niche representation and the environmental variational inference (ENVI) data integration method model phenotype–microenvironment interplay and reconstruct the spatial context of dissociated single-cell RNA sequencing datasets.

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