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使用光可裂解生物素的DNA基质辅助激光解吸/电离质谱分析

Matrix-assisted laser desorption/ionization mass spectrometry of DNA using photocleavable biotin.

作者信息

Hahner S, Olejnik J, Lüdemann H C, Krzymañska-Olejnik E, Hillenkamp F, Rothschild K J

机构信息

AmberGen, Inc., Boston, MA 02215, USA.

出版信息

Biomol Eng. 1999 Dec 31;16(1-4):127-33. doi: 10.1016/s1050-3862(99)00049-2.

Abstract

Oligonucleotides containing a photocleavable biotin (5'-PC-biotin) were analyzed by matrix assisted laser desorption/ionization mass spectrometry (MALDI-MS) with wavelengths in the ultraviolet (UV) and infrared (IR) from solution and after capture on streptavidin-coated agarose or magnetic beads. The analysis was used to monitor the release of the oligonucleotides as a result of photochemical cleavage of the biotinylated linker. Near-UV pulses (UV-MALDI) led to predominant release of the photocleaved product. In contrast, only the uncleaved analyte was detected using IR pulses (IR-MALDI). Results from MALDI analysis are also presented for DNA containing a photocleavable 5'-amino group which can be covalently linked to a variety of activated surfaces and marker molecules. In a demonstration of this approach, a 5'-PC-biotinylated 49 nt RNA oligonucleotide was enzymatically synthesized using a PC-biotin-r(AG) dinucleotide primer, captured on streptavidin coated magnetic beads and analyzed by UV-MALDI. Potential applications of photocleavable linkers combined with MALDI for the analysis of nucleic acids are discussed.

摘要

含有可光裂解生物素(5'-PC-生物素)的寡核苷酸,通过基质辅助激光解吸/电离质谱(MALDI-MS)进行分析,该质谱采用来自溶液以及捕获在链霉亲和素包被的琼脂糖或磁珠上后的紫外(UV)和红外(IR)波长。该分析用于监测由于生物素化连接子的光化学裂解而导致的寡核苷酸释放。近紫外脉冲(UV-MALDI)导致光裂解产物的主要释放。相比之下,使用红外脉冲(IR-MALDI)仅检测到未裂解的分析物。还展示了含有可光裂解5'-氨基基团的DNA的MALDI分析结果,该基团可共价连接到各种活化表面和标记分子。在这种方法的一个实例中,使用PC-生物素-r(AG)二核苷酸引物酶促合成了一个5'-PC-生物素化的49 nt RNA寡核苷酸,将其捕获在链霉亲和素包被的磁珠上并通过UV-MALDI进行分析。讨论了可光裂解连接子与MALDI相结合用于核酸分析的潜在应用。

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