Gaytán Paul, Roldán-Salgado Abigail
Instituto de Biotecnología, Universidad Nacional Autónoma de México, Av. Universidad 2001, Col. Chamilpa, Cuernavaca, Morelos 62210, Mexico.
ACS Omega. 2024 Jun 14;9(26):28577-28582. doi: 10.1021/acsomega.4c02603. eCollection 2024 Jul 2.
Photoactivatable and photoswitchable fluorescent proteins (FPs) are sophisticated molecular tools that in combination with super-resolution microscopy are helping to elucidate many biological processes. Through the Y66H mutation in the chromophore of the violet fluorescent protein SumireF, we created the first photoactivatable blue fluorescent protein (PA-BFP). This protein is rapidly activated over ordinary UV transilluminators at 302 or 365 nm in irreversible mode and by direct exposition to sunlight. The maximum excitation and emission wavelengths of this protein, centered at 358 and 445 nm, respectively, resemble the values of DAPI-the blue stain widely used in fluorescence microscopy to visualize nucleic acids in cells. Therefore, the immediate use of PA-BFP in cellular biology is clear because the technology required to follow this new genetically encoded reporter at the microscopic level has already been established. PA-BFP can potentially be used together with other photoactivatable fluorescent proteins of different colors to label multiple proteins, which can be simultaneously tracked by advanced microscopic techniques.
光激活和光开关荧光蛋白(FPs)是复杂的分子工具,与超分辨率显微镜结合有助于阐明许多生物过程。通过对紫色荧光蛋白SumireF发色团进行Y66H突变,我们创建了首个光激活蓝色荧光蛋白(PA-BFP)。该蛋白在302或365nm的普通紫外透照仪下以不可逆模式快速激活,也可通过直接暴露在阳光下激活。该蛋白的最大激发和发射波长分别为358和445nm,与DAPI的值相似——DAPI是荧光显微镜中广泛用于可视化细胞内核酸的蓝色染料。因此,PA-BFP在细胞生物学中的直接应用显而易见,因为在微观水平追踪这种新的基因编码报告分子所需的技术已经建立。PA-BFP有可能与其他不同颜色的光激活荧光蛋白一起用于标记多种蛋白质,这些蛋白质可以通过先进的显微镜技术同时进行追踪。