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A fluorescent natural product for ultra sensitive detection of proteins in one‐dimensional and two‐dimensional gel electrophoresis
Author(s) -
Mackintosh James A.,
Choi HungYoon,
Bae SooHan,
Veal Duncan A.,
Bell Philip J.,
Ferrari Belinda C.,
Van Dyk Derek D.,
Verrills Nicole M.,
Paik YoungKi,
Karuso Peter
Publication year - 2003
Publication title -
proteomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.26
H-Index - 167
eISSN - 1615-9861
pISSN - 1615-9853
DOI - 10.1002/pmic.200300578
Subject(s) - chemistry , fluorescence , analytical chemistry (journal) , mass spectrometry , fluorophore , chromatography , optics , physics
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.