Optimizing multifunctional fluorescent ligands for intracellular labeling.

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Proc Natl Acad Sci U S A. 2025 Nov 04;122(44):e2510046122. doi: 10.1073/pnas.2510046122

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Optimizing multifunctional fluorescent ligands for intracellular labeling. Lavis Lab

Kumar P, Vevea JD, Tkachuk AN, Campbell KR, Watson ET, Ayala AX, Grimm JB, Chapman ER, Solecki DJ, Lavis LD

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Abstract

Enzyme-based self-labeling tags enable the covalent attachment of synthetic molecules to proteins inside living cells. A frontier of this field is designing cell-permeable multifunctional ligands that contain fluorophores in combination with affinity tags or pharmacological agents. This is challenging since attachment of additional chemical moieties onto fluorescent ligands can adversely affect membrane permeability. To address this problem, we examined the chemical properties of rhodamine-based self-labeling tag ligands through the lens of medicinal chemistry. We found that the lactone-zwitterion equilibrium constant () of rhodamines inversely correlates with their distribution coefficients (log), suggesting that ligands based on dyes exhibiting low and high log values, such as Si-rhodamines, would efficiently enter cells. We designed cell-permeable multifunctional HaloTag ligands with a biotin moiety to purify mitochondria or a JQ1 appendage to translocate BRD4 within the nucleus. We found that translocation of BRD4 to constitutive heterochromatin in cells leads to apparent increases in transcriptional activity. These fluorescent reagents enable affinity capture and translocation of intracellular proteins in living cells, and our general design concepts will facilitate the design of multifunctional chemical tools for biology.

Preprint: https://doi.org/10.1101/2022.07.02.498544
Preprint: https://doi.org/10.32388/0xcyuc