Dual SLIPT–A Lipid Mimic to Enable Spatiotemporally Defined, Sequential Protein Dimerization

Spatiotemporal control of proteins is crucial for cellular phenomena such as signal integration, propagation, as well as managing crosstalk. In membrane-associated signaling, this regulation is often enabled by lipids, wherein highly dynamic, sequential recruitment of interacting proteins is key to successful signaling. Here, we present dual SLIPT (self-localizing ligand-induced protein translocation), a lipid-analog tool, capable of emulating this lipid-mediated sequential recruitment of any two proteins of interest. Dual SLIPT self-localizes to the inner leaflet of the plasma membrane (PM). There, dual SLIPT presents trimethoprim (TMP) and HaloTag ligand (HTL) to cytosolic proteins of interest (POIs), whereupon POIs fused to the protein tags <sup>iK6</sup>eDHFR, or to HOB are recruited. A systematic extension of the linkers connecting the two mutually orthogonal headgroups was implemented to overcome the steric clash between the recruited POIs. Using Förster resonance energy transfer (FRET), we verify that the resulting probe is capable of simultaneous binding of both proteins of interest, as well as their dimerization. Dual SLIPT was found to be particularly suitable for use in physiologically relevant concentrations, such as recruitment via tightly regulated, transient lipid species. We further expanded dual SLIPT to the photocontrollable dual SLIPT<sup>NVOC</sup>, by introducing a photocaging group onto the TMP moiety. Dual SLIPT<sup>NVOC</sup> enables sequential and spatiotemporally defined dimerization upon blue light irradiation. Thus, dual SLIPT<sup>NVOC</sup> serves as a close mimic of physiology, enabling interrogation of dynamic cytosol-to-plasma membrane recruitment events and their impact on signaling.

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Journal
ACS Chemical Biology
Published
2025-04-15
DOI
https://doi.org/10.1021/acschembio.4c00856
Citations
1
Primary Topic
RNA and protein synthesis mechanisms
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article
Field-Weighted Citation Impact
0.81
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article

Dual SLIPT–A Lipid Mimic to Enable Spatiotemporally Defined, Sequential Protein Dimerization

M. Taeb, Shige H. Yoshimura, Richard Wombacher, Birgit Koch et al.
1 citations
ACS Chemical Biology
RNA and protein synthesis mechanisms
0.81
article

Dual SLIPT–A Lipid Mimic to Enable Spatiotemporally Defined, Sequential Protein Dimerization

M. Taeb, Shige H. Yoshimura, Richard Wombacher, Birgit Koch, Kristina Viktoria Bayer
article en
1 citations

Abstract

Spatiotemporal control of proteins is crucial for cellular phenomena such as signal integration, propagation, as well as managing crosstalk. In membrane-associated signaling, this regulation is often enabled by lipids, wherein highly dynamic, sequential recruitment of interacting proteins is key to successful signaling. Here, we present dual SLIPT (self-localizing ligand-induced protein translocation), a lipid-analog tool, capable of emulating this lipid-mediated sequential recruitment of any two proteins of interest. Dual SLIPT self-localizes to the inner leaflet of the plasma membrane (PM). There, dual SLIPT presents trimethoprim (TMP) and HaloTag ligand (HTL) to cytosolic proteins of interest (POIs), whereupon POIs fused to the protein tags <sup>iK6</sup>eDHFR, or to HOB are recruited. A systematic extension of the linkers connecting the two mutually orthogonal headgroups was implemented to overcome the steric clash between the recruited POIs. Using Förster resonance energy transfer (FRET), we verify that the resulting probe is capable of simultaneous binding of both proteins of interest, as well as their dimerization. Dual SLIPT was found to be particularly suitable for use in physiologically relevant concentrations, such as recruitment via tightly regulated, transient lipid species. We further expanded dual SLIPT to the photocontrollable dual SLIPT<sup>NVOC</sup>, by introducing a photocaging group onto the TMP moiety. Dual SLIPT<sup>NVOC</sup> enables sequential and spatiotemporally defined dimerization upon blue light irradiation. Thus, dual SLIPT<sup>NVOC</sup> serves as a close mimic of physiology, enabling interrogation of dynamic cytosol-to-plasma membrane recruitment events and their impact on signaling.

ACS Chemical BiologyVol. 20(5)
Kyoto University (JP), Heidelberg University (DE), Max Planck Institute for Medical Research (DE), Material Sciences (United States) (US), Living Systems (United States) (US)
Zero hunger
Openalex Percentile: Top 29%
RNA and protein synthesis mechanisms
0.81
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