Lee Clement M
Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai;
J Vis Exp. 2016 Feb 14(108):53632. doi: 10.3791/53632.
Fluorescence microscopy is employed to identify Kinesin-1 cargos. Recently, the heavy chain of Kinesin-1 (KIF5B) was shown to transport the nuclear transcription factor c-MYC for proteosomal degradation in the cytoplasm. The method described here involves the study of a motorless KIF5B mutant for fluorescence microscopy. The wild-type and motorless KIF5B proteins are tagged with the fluorescent protein tdTomato. The wild-type tdTomato-KIF5B appears homogenously in the cytoplasm, while the motorless tdTomato-KIF5B mutant forms aggregates in the cytoplasm. Aggregation of the motorless KIF5B mutant induces aggregation of its cargo c-MYC in the cytoplasm. Hence, this method provides a visual means to identify the cargos of Kinesin-1. A similar strategy can be utilized to identify cargos of other motor proteins.
荧光显微镜被用于识别驱动蛋白-1的货物蛋白。最近,有研究表明驱动蛋白-1的重链(KIF5B)可将核转录因子c-MYC转运至细胞质中进行蛋白酶体降解。本文所述方法涉及对用于荧光显微镜研究的无运动能力的KIF5B突变体进行研究。野生型和无运动能力的KIF5B蛋白都用荧光蛋白tdTomato进行标记。野生型tdTomato-KIF5B在细胞质中均匀分布,而无运动能力的tdTomato-KIF5B突变体则在细胞质中形成聚集体。无运动能力的KIF5B突变体的聚集会诱导其货物蛋白c-MYC在细胞质中聚集。因此,该方法提供了一种可视化手段来识别驱动蛋白-1的货物蛋白。类似的策略可用于识别其他运动蛋白的货物蛋白。