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bioRxiv · 10.1101/2023.09.14.557726

Rapid optogenetic clustering of a cytoplasmic BcLOV4 variant

Abstract

Protein clustering is a powerful form of optogenetic control, yet there is currently only one protein --Cry2--whose light-induced clustering has been harnessed for these purposes. Recently, the photoreceptor BcLOV4 was found to form protein clusters in mammalian cells in response to blue light, although clustering coincided with its translocation to the plasma membrane, potentially constraining its application as an optogenetic clustering module. Herein we identify key amino acids that couple clustering to membrane binding, allowing us to engineer a variant of BcLOV4 that clusters in the cytoplasm and does not associate with the membrane in response to blue light. This variant, BcLOVclust, clustered over many cycles with dramatically faster clustering and de-clustering kinetics compared to Cry2. The magnitude of BcLOVclust clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by optimizing the fluorescent protein to which it was fused. BcLOVclust retained the temperature sensitivity of BcLOV4 such that light induced clustering was transient, and the rate of spontaneous declustering increased with temperature. At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates. BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells. Thus BcLOVclust provides an alternative to Cry2 for optogenetic clustering and a method for multiplexed clustering. While its usage is currently suited for organisms that can be cultured below [~]30 {degrees}C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=163 SRC="FIGDIR/small/557726v1_ufig1.gif" ALT="Figure 1"> View larger version (31K): org.highwire.dtl.DTLVardef@15e80f3org.highwire.dtl.DTLVardef@163d54corg.highwire.dtl.DTLVardef@1489845org.highwire.dtl.DTLVardef@10505c1_HPS_FORMAT_FIGEXP M_FIG C_FIG HighlightsO_LILight-responsive clustering of BcLOV4 can be decoupled from its membrane association C_LIO_LIBcLOVclust clusters in the cytoplasm with faster ON and OFF kinetics than Cry2 C_LIO_LIBcLOVclust and Cry2 can be multiplexed in the same cell C_LIO_LIBcLOVclust can control RhoA activity and stress granule formation C_LI

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BibTeXRIS

Huang, Z., Benman, W., Dong, L., Bugaj, L. J.. 2023-09-17. Rapid optogenetic clustering of a cytoplasmic BcLOV4 variant. https://doi.org/10.1101/2023.09.14.557726

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