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

被引:94
作者
Mackintosh, JA
Choi, HY
Bae, SH
Veal, DA
Bell, PJ
Ferrari, BC
Van Dyk, DD
Verrills, NM
Paik, YK
Karuso, P [1 ]
机构
[1] Macquarie Univ, Dept Chem, FLUOROtech Pty Ltd, Sydney, NSW 2109, Australia
[2] Yonsei Univ, Proteome Res Ctr, Seoul 120749, South Korea
[3] Yonsei Univ, Dept Biochem, Seoul 120749, South Korea
[4] Macquarie Univ, Dept Biol Sci, Sydney, NSW 2109, Australia
[5] Macquarie Univ, Australian Proteome Anal Facil, Sydney, NSW 2109, Australia
[6] Macquarie Univ, Dept Chem, Sydney, NSW 2109, Australia
关键词
electrophoresis; fluorescence; mass spectrometry; natural product; SYPRO;
D O I
10.1002/pmic.200300578
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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 nrn 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 nrn Argon-ion lasers; 473 nrn 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.
引用
收藏
页码:2273 / 2288
页数:16
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