Grinstead Kristen M, Rowe Laura, Ensor Charles M, Joel Smita, Daftarian Pirouz, Dikici Emre, Zingg Jean-Marc, Daunert Sylvia
Department of Biochemistry and Molecular Biology, R. Bunn Gautier Bldg., 1011 NW 15th Street, Miller School of Medicine, University of Miami, Miami, FL, 33136, United States of America.
Department of Chemistry, 1610 Campus Drive East, Valparaiso University, Valparaiso, IN, 46385, United States of America.
PLoS One. 2016 Jul 1;11(7):e0158579. doi: 10.1371/journal.pone.0158579. eCollection 2016.
The increased importance of in vivo diagnostics has posed new demands for imaging technologies. In that regard, there is a need for imaging molecules capable of expanding the applications of current state-of-the-art imaging in vivo diagnostics. To that end, there is a desire for new reporter molecules capable of providing strong signals, are non-toxic, and can be tailored to diagnose or monitor the progression of a number of diseases. Aequorin is a non-toxic photoprotein that can be used as a sensitive marker for bioluminescence in vivo imaging. The sensitivity of aequorin is due to the fact that bioluminescence is a rare phenomenon in nature and, therefore, it does not suffer from autofluorescence, which contributes to background emission. Emission of bioluminescence in the blue-region of the spectrum by aequorin only occurs when calcium, and its luciferin coelenterazine, are bound to the protein and trigger a biochemical reaction that results in light generation. It is this reaction that endows aequorin with unique characteristics, making it ideally suited for a number of applications in bioanalysis and imaging. Herein we report the site-specific incorporation of non-canonical or non-natural amino acids and several coelenterazine analogues, resulting in a catalog of 72 cysteine-free, aequorin variants which expand the potential applications of these photoproteins by providing several red-shifted mutants better suited to use in vivo. In vivo studies in mouse models using the transparent tissue of the eye confirmed the activity of the aequorin variants incorporating L-4-iodophehylalanine and L-4-methoxyphenylalanine after injection into the eye and topical addition of coelenterazine. The signal also remained localized within the eye. This is the first time that aequorin variants incorporating non-canonical amino acids have shown to be active in vivo and useful as reporters in bioluminescence imaging.
体内诊断重要性的日益增加对成像技术提出了新的要求。在这方面,需要能够扩展当前最先进的体内诊断成像应用的成像分子。为此,人们期望有新的报告分子,它们能够提供强信号、无毒,并且能够针对多种疾病的诊断或病情进展监测进行定制。水母发光蛋白是一种无毒的光蛋白,可作为体内成像生物发光的灵敏标记物。水母发光蛋白的灵敏度源于生物发光在自然界中是一种罕见现象这一事实,因此它不存在自体荧光问题,而自体荧光会导致背景发射。只有当钙及其荧光素腔肠素与该蛋白结合并引发导致发光的生化反应时,水母发光蛋白才会在光谱的蓝光区域发出生物发光。正是这种反应赋予了水母发光蛋白独特的特性,使其非常适合生物分析和成像中的多种应用。在此我们报告了非标准或非天然氨基酸以及几种腔肠素类似物的位点特异性掺入,从而得到了72种不含半胱氨酸的水母发光蛋白变体目录,这些变体通过提供几种更适合体内使用的红移突变体扩展了这些光蛋白的潜在应用。使用小鼠眼睛透明组织进行的体内研究证实,在向眼睛注射并局部添加腔肠素后,掺入L-4-碘苯丙氨酸和L-4-甲氧基苯丙氨酸的水母发光蛋白变体具有活性。信号也保留在眼睛内。这是首次证明掺入非标准氨基酸的水母发光蛋白变体在体内具有活性并可作为生物发光成像中的报告分子。