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一种用于一维和二维凝胶电泳中蛋白质超灵敏检测的荧光天然产物。

A fluorescent natural product for ultra sensitive detection of proteins in one-dimensional and two-dimensional gel electrophoresis.

作者信息

Mackintosh James A, Choi Hung-Yoon, Bae Soo-Han, Veal Duncan A, Bell Philip J, Ferrari Belinda C, Van Dyk Derek D, Verrills Nicole M, Paik Young-Ki, Karuso Peter

机构信息

FLUOROtechnics Pty Ltd., Department of Chemistry, Macquarie University, Sydney, NSW 2109, Australia.

出版信息

Proteomics. 2003 Dec;3(12):2273-88. doi: 10.1002/pmic.200300578.

Abstract

Lightning Fast is a sensitive fluorescence-based stain for detecting proteins in one-dimensional and two-dimensional polyacrylamide electrophoresis gels. It contains the fluorophore epicocconone from the fungus Epicoccum nigrum that interacts noncovalently with sodium dodecyl sulfate and protein. Stained proteins can be excited optimally by near-ultraviolet light of about 395 nm or with visible light of about 520 nm. The stain can be excited using a range of sources used in image analysis systems including UVA (ca. 365 nm) and UVB (ca. 302 nm) transilluminators; Xenon-arc lamps; 488 nm and 457 nm Argon-ion lasers; 473 nm and 532 nm neodymium: yttrium aluminum garnet (Nd:YAG) solid-state lasers; 543 nm helium-neon lasers, and emerging violet, blue and green diode lasers. Maximum fluorescence emission of the dye is at approximately 610 nm. The limit of detection in one-dimensional gels stained with Lightning Fast protein gel stain is less than 100 pg of protein, rivaling the current limits of matrix-assisted laser desorption/ionization-mass spectrometry (MALDI-MS). Lightning Fast was found to be considerably more sensitive than SYPRO Ruby, SYPRO Orange, silver and Coomassie Brilliant Blue G-250 in matched experiments. Staining takes as little as 3.5 h and stained proteins displayed quantitative linearity over more than four orders of magnitude, thereby allowing visualization of entire proteomes. Lightning Fast protein gel staining is compatible with subsequent peptide mass fingerprinting using MALDI-MS and Edman-based sequencing chemistry.

摘要

“闪电快染”是一种基于荧光的灵敏染色剂,用于检测一维和二维聚丙烯酰胺电泳凝胶中的蛋白质。它含有来自真菌黑附球菌的荧光团表球壳菌素,该荧光团与十二烷基硫酸钠和蛋白质非共价相互作用。染色后的蛋白质可以用约395nm的近紫外光或约520nm的可见光进行最佳激发。该染色剂可以使用图像分析系统中使用的一系列光源进行激发,包括UVA(约365nm)和UVB(约302nm)透照仪;氙弧灯;488nm和457nm氩离子激光器;473nm和532nm钕:钇铝石榴石(Nd:YAG)固态激光器;543nm氦氖激光器,以及新兴的紫光、蓝光和绿光二极管激光器。该染料的最大荧光发射波长约为610nm。用“闪电快染”蛋白质凝胶染色剂染色的一维凝胶中的检测限小于100pg蛋白质,可与当前基质辅助激光解吸/电离质谱(MALDI-MS)的检测限相媲美。在匹配实验中,发现“闪电快染”比SYPRO Ruby、SYPRO Orange、银染和考马斯亮蓝G-250灵敏得多。染色只需3.5小时,染色后的蛋白质在超过四个数量级上显示出定量线性,从而可以可视化整个蛋白质组。“闪电快染”蛋白质凝胶染色与随后使用MALDI-MS的肽质量指纹分析和基于埃德曼的测序化学兼容。

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