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单体远红和近红外高亮度荧光胆红素蛋白。

Monomeric Far-red and Near-infrared Fluorescent Biliproteins of Ultrahigh Brightness.

机构信息

National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, 430070, P.R. China.

出版信息

Chembiochem. 2024 Jun 3;25(11):e202400068. doi: 10.1002/cbic.202400068. Epub 2024 May 14.

Abstract

Far-red and near-infrared fluorescent proteins have regions of maximum transmission in most tissues and can be widely used as fluorescent biomarkers. We report that fluorescent phycobiliproteins originating from the phycobilisome core subunit ApcF2 can covalently bind biliverdin, named BDFPs. To further improve BDFPs, we conducted a series of studies. Firstly, we mutated K53Q and T144A of BDFPs to increase their effective brightness up to 190 % in vivo. Secondly, by homochromatic tandem fusion of high-brightness BDFPs to achieve monomerization, which increases the effective brightness by up to 180 % in vivo, and can effectively improve the labeling effect. By combining the above two approaches, the brightness of the tandem BDFPs was much improved compared with that of the previously reported fluorescent proteins in a similar spectral range. The tandem BDFPs were expressed stably while maintaining fluorescence in mammalian cells and Caenorhabditis elegans. They were also photostable and resistant to high temperature, low pH, and chemical denaturation. The tandem BDFPs advantages were proved in applications as biomarkers for imaging in super-resolution microscopy.

摘要

远红和近红外荧光蛋白在大多数组织中有最大的透射区域,可广泛用作荧光生物标志物。我们报告说,源自藻胆体核心亚基 ApcF2 的荧光藻胆蛋白可以与胆绿素共价结合,命名为 BDFP。为了进一步提高 BDFP 的性能,我们进行了一系列研究。首先,我们对 K53Q 和 T144A 进行突变,使 BDFP 的有效亮度在体内提高了 190%。其次,通过高亮度 BDFP 的同色串联融合实现单体化,使体内有效亮度提高了 180%,可以有效提高标记效果。通过结合这两种方法,串联 BDFP 的亮度与类似光谱范围内之前报道的荧光蛋白相比有了很大的提高。串联 BDFP 在哺乳动物细胞和秀丽隐杆线虫中稳定表达,同时保持荧光。它们还具有光稳定性,能够耐受高温、低 pH 值和化学变性。串联 BDFP 在超分辨率显微镜成像的生物标志物应用中得到了验证。

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