Institut de Science et Ingénierie Supramoléculaires (ISIS-UMR 7006), Université de Strasbourg, CNRS, 8 allée Gaspard Monge, 67000 Strasbourg, France.
Chemistry. 2013 Jun 17;19(25):8182-9. doi: 10.1002/chem.201300060. Epub 2013 Apr 30.
Reactions templated by cellular nucleic acids are attractive for nucleic acid sensing or responsive systems. Herein we report the use of a photocatalyzed reductive cleavage of an immolative linker to unmask a rhodamine fluorophore, and its application to miRNA imaging. The reaction was found to proceed with a very high turnover (>4000) and provided reliable detection down to 5 pM of template by using γ-serine-modified peptide nucleic acid (PNA) probes. The reaction was used for the selective detection of miR-21 in BT474 cells and miR-31 in HeLa cells following irradiation for 30 min. The probes were introduced by using reversible permeation with streptolysin-O (SLO) or a transfection technique.
细胞核酸模板反应在核酸传感或响应系统中很有吸引力。本文报道了用光催化还原裂解无活性连接物来解屏蔽罗丹明荧光团的方法,并将其应用于 miRNA 成像。反应具有非常高的周转率(>4000),通过使用γ-丝氨酸修饰的肽核酸(PNA)探针,可以可靠地检测低至 5 pM 的模板。该反应用于在 BT474 细胞中选择性检测 miR-21 和在 HeLa 细胞中选择性检测 miR-31,在照射 30 分钟后进行。探针通过使用链球菌溶血素 O(SLO)的可逆渗透或转染技术引入。