Kolpashchikov Dmitry M
Division of Experimental Therapeutics, Department of Medicine, Columbia University, Box 84, 630W 168th Street, New York, New York 10032, USA.
J Am Chem Soc. 2005 Sep 14;127(36):12442-3. doi: 10.1021/ja0529788.
A new probe that can fluorescently report the presence of specific nucleic acids in solution with extremely high selectivity was developed. The probe consists of malachite green-a triphenylmethane dye-and two short RNA strands, each of which comprises a fragment complementary to an analyte molecule and a fragment of a malachite green aptamer (MGA). The two RNA strands form MGA upon hybridization to the adjacent positions of the nucleic acid analyte. MGA is able to bind malachite green and enhance the fluorescence of the dye, thus monitoring the presence of the nucleic acid in solution. The probe reliably discriminates against 41 out of 42 possible single nucleotide substitutions in 14-mer DNA analyte at room temperature in physiological buffer. Consisting of unmodified RNA strands, which can be expressed in living cells, binary MGA probe represents a promising instrument for real-time nucleic acid monitoring in vivo.
开发出了一种新型探针,它能够以极高的选择性荧光报告溶液中特定核酸的存在。该探针由孔雀石绿(一种三苯甲烷染料)和两条短RNA链组成,每条RNA链都包含与分析物分子互补的片段和孔雀石绿适体(MGA)的片段。两条RNA链在与核酸分析物的相邻位置杂交时形成MGA。MGA能够结合孔雀石绿并增强染料的荧光,从而监测溶液中核酸的存在。在生理缓冲液中室温下,该探针能可靠地区分14聚体DNA分析物中42种可能的单核苷酸替换中的41种。由可在活细胞中表达的未修饰RNA链组成的二元MGA探针是一种用于体内实时核酸监测的有前景的工具。