Continuous free-flow electrophoresis separation of cytosolic proteins from the human colon carcinoma cell line LIM 1215: A non two-dimensional gel electrophoresis-based proteome analysis strategy

Hoffmann, P; Ji, H; Moritz, RL; Connolly, LM; Frecklington, DF; Layton, MJ; Eddes, JS; Simpson, RJ

Author(s): Hoffmann, P; Ji, H; Moritz, RL; Connolly, LM; Frecklington, DF; Layton, MJ; Eddes, JS; Simpson, RJ;
Details: Publication Year 2001-07,Volume 1,Issue #7,Page 807-818
Journal Title: PROTEOMICS
Publication Type: Journal Article
Abstract: The conventional approach for analyzing the protein complement of a genome involves the combination of two-dimensional gel electrophoresis (2-DE) and mass spectrometric based protein identification technologies. While 2-DE is a powerful separation technique, it is severely limited by the insolubility of certain classes of proteins (e.g. hydrophobic membrane proteins), as well as the amount of protein that can be processed. Here, we describe a simple procedure for resolving complex mixtures of proteins that involves a combination of free flow electrophoresis (FFE), a liquid-based isoelectric focussing (IEF) method, and sodium doclecylsulfate-polyacrylamide gel electrophoresis (SDS-PAGE). Resolved proteins were identified by peptide fragment sequencing using capillary column reversed-phase high performance liquid chromatography (RP-HPLC)/mass spectrometry (MS). An initial demonstration of the method was performed using digitonin/ethylenediaminetetraacetic acid EDTA extracted cytosolic proteins from the human colon carcinoma cell line, LIM 1215. Cytosolic proteins were separated by liquid-based IEF (pH range 3-10) into 96 fractions, and each FFE fraction was further fractionated by SDS-PAGE. Selected protein bands were excised from the SDS-PAGE gel, digested in situ with trypsin, and subsequently identified by on-line RP-HPLC/electrospray-ionization ion trap MS. Our results indicate that FIFE is: (i) an extremely powerful liquid-based IEF method for resolving proteins; (ii) not limited by the amount of sample that can be loaded onto the instrument; and (iii) capable of fractionating intact protein complexes (a potentially powerful tool for cell-mapping proteomics). An up-to-date list of cytosolic proteins from the human colorectal carcinoma cell line LIM 1215 can be found in the Joint Protein Structure Laboratory (JPSL) proteome database. This information will provide an invaluable resource for future proteomics-based biological studies of colon cancer. The JPSL proteome database can be accessed through the World Wide Web (WWW) network (http://www.ludwig.edu.au/ jpsl/jpslhome.html).
Publisher: WILEY-V C H VERLAG GMBH
Keywords: ASSISTED-LASER-DESORPTION/IONIZATION; PERFORMANCE LIQUID-CHROMATOGRAPHY; AMINO-ACID-SEQUENCES; MASS-SPECTROMETRY; DATABASE; PEPTIDES; STATHMIN; LIM-1215; CRYPTS
Publisher's Version: https://doi.org/10.1002/1615-9861(200107)1:7<807::AID-PROT807>3.0.CO;2-6
Terms of Use/Rights Notice: Refer to copyright notice on published article.

Creation Date: 2001-07-01 12:00:00