Center for Biosignatures Discovery Automation, Biodesign Institute, Arizona State University, 1001 McAllister Ave, Tempe, AZ 85287, USA.
Biomaterials. 2010 Oct;31(29):7411-22. doi: 10.1016/j.biomaterials.2010.06.023. Epub 2010 Jul 8.
A series of new naphthalimide derivatives were synthesized and studied. Three of the materials (SM1, SM2, and SM3) possess methacrylate(s) moieties as pH sensor monomers, enabling these compounds to be polymerized with other monomers for thin film preparation for extracellular pH sensing. Herein, poly(2-hydroxyethyl methacrylate)-co-poly(acrylamide) (PHEMA-co-PAM) was chosen as the polymer matrix. Structure influences on pH responses and pK(a) values were studied. The film P3 composed of the sensing moiety SM3 has a pK(a) close to the usual biological environmental pH of approximately 7. It was used as an extracellular pH sensor to monitor pH change during the metabolism of prokaryotic Escherichia coli (E. coil). On the other hand, the three sensor monomers are new intracellular biomarkers to sense lysosomes of eukaryotic cells since (1) their pK(a) values are in a range of 5.9-6.8; (2) their emission intensities at acidic conditions (such as at pH 5) are much stronger than those at a neutral condition of pH 7; (3) lysosomes range in size from 0.1 to 1.2 mum in diameter with pH ranging from 4.5 to 5.0, which is much more acidic than the pH value of the cytoplasm (usually with a pH value of approximately 7.2); and (4) the acidity of lysosomes enables a protonation of the amino groups of the pH probes making the sensors emit brightly in acidic organelles by inhibiting the photo-induced electron transfer from the amino groups to the fluorophores. Lysosome sensing was demonstrated using live human brain glioblastoma U87MG cell line, human cervical cancer HeLa cell line, and human esophagus premalignant CP-A and CP-D cell lines by observations of small acidic spherical organelles (lysosomes) and significant colocalizations (82-95%) of the sensors with a commercially available lysosome-selective staining probe LysoTracker Red under confocal fluorescence microscopy.
合成并研究了一系列新的萘二甲酰亚胺衍生物。其中三种材料(SM1、SM2 和 SM3)具有作为 pH 传感器单体的甲基丙烯酯部分,使得这些化合物能够与其他单体聚合以制备用于细胞外 pH 传感的薄膜。在此,选择聚(2-羟乙基甲基丙烯酸酯)-共-聚(丙烯酰胺)(PHEMA-co-PAM)作为聚合物基质。研究了结构对 pH 响应和 pK(a)值的影响。由传感部分 SM3 组成的薄膜 P3 的 pK(a)接近约 7 的通常生物环境 pH。它被用作细胞外 pH 传感器,以监测原核大肠杆菌(E. coil)代谢过程中的 pH 变化。另一方面,这三种传感器单体是新的细胞内生物标志物,可用于检测真核细胞的溶酶体,原因是:(1) 它们的 pK(a) 值在 5.9-6.8 范围内;(2) 在酸性条件(如 pH 5)下的发射强度比在中性条件(pH 7)下强得多;(3) 溶酶体的直径从 0.1 到 1.2 µm,pH 值从 4.5 到 5.0,比细胞质的 pH 值(通常约为 7.2)酸性大得多;(4) 溶酶体的酸度使 pH 探针的氨基质子化,通过抑制从氨基到荧光团的光致电子转移,使传感器在酸性细胞器中发出明亮的光。通过观察小的酸性球形细胞器(溶酶体)和传感器与商业上可用的溶酶体选择性染色探针 LysoTracker Red 的显著共定位(82-95%),用人脑神经胶质瘤 U87MG 细胞系、人宫颈癌 HeLa 细胞系和人食管癌前病变 CP-A 和 CP-D 细胞系证实了溶酶体的传感。共聚焦荧光显微镜。