Medicum, Faculty of Medicine, University of Helsinki, 00290 Helsinki, Finland.
Department of Genetics and Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Int J Mol Sci. 2023 Mar 30;24(7):6526. doi: 10.3390/ijms24076526.
Optogenetic systems driven by yellow-orange light are required for the simultaneous regulation of several cellular processes. We have engineered the red fluorescent protein FusionRed into a 26 kDa monomeric optogenetic module, called degFusionRed. Unlike other fluorescent protein-based optogenetic domains, which exhibit light-induced self-inactivation by generating reactive oxygen species, degFusionRed undergoes proteasomal degradation upon illumination with 567 nm light. Similarly to the parent protein, degFusionRed has minimal absorbance at 450 nm and above 650 nm, making it spectrally compatible with blue and near-infrared-light-controlled optogenetic tools. The autocatalytically formed chromophore provides degFusionRed with an additional advantage over most optogenetic tools that require the binding of the exogenous chromophores, the amount of which varies in different cells. The degFusionRed efficiently performed in the engineered light-controlled transcription factor and in the targeted photodegradation of the protein of interest, demonstrating its versatility as the optogenetic module of choice for spectral multiplexed interrogation of various cellular processes.
需要使用黄橙色光驱动的光遗传学系统来同时调节多个细胞过程。我们将红色荧光蛋白 FusionRed 工程化为一个 26 kDa 的单体光遗传学模块,称为 degFusionRed。与其他基于荧光蛋白的光遗传学结构域不同,这些结构域通过产生活性氧而发生光诱导的自我失活,而 degFusionRed 在受到 567nm 光照射时会经历蛋白酶体降解。与母体蛋白相似,degFusionRed 在 450nm 以上和 650nm 以上的光吸收最小,使其与蓝光和近红外光控制的光遗传学工具在光谱上兼容。自催化形成的生色团使 degFusionRed 具有相对于大多数光遗传学工具的另一个优势,大多数光遗传学工具需要结合外源生色团,而外源生色团在不同细胞中的含量不同。degFusionRed 在工程化的光控转录因子中以及在目标蛋白的光降解中都能有效地发挥作用,证明了它作为光遗传学模块的多功能性,可用于对各种细胞过程进行光谱多路复用检测。