Abstract
Mass spectrometry and peptide-centric approaches are powerful techniques for the identification of differentially expressed proteins. Despite enormous improvements in MS technologies, sample preparation and efficient fractionation of target analytes are still major bottlenecks in MS-based protein analysis. The complexity of tryptically digested whole proteomes needs to be considerably reduced before low abundance proteins can be effectively analyzed using MS/MS. Sample preparation strategies that use peptide-specific antibodies are able to reduce the complexity of tryptic digests and lead to a substantial increase in throughput and sensitivity; however, the number of peptide-specific capture reagents is low, and consequently immunoaffinity-based approaches are only capable of detecting small sets of protein-derived peptides. In this proof-of-principle study, special anti-peptide antibodies were used to enrich peptides from a complex mixture. These antibodies recognize short amino acid sequences that are found directly at the termini of the peptides. The recognized epitopes consist of three or four amino acids only and include the terminally charged group of the peptide. Because of its limited length, antibodies recognizing the epitope will enrich not only one peptide but a whole class of peptides that share this terminal epitope. In this study, β-catenin-derived peptides were used to demonstrate that it is possible (i) to effectively generate antibodies that recognize short C-terminal peptide epitopes and (ii) to enrich and identify peptide classes from a complex mixture using these antibodies in an immunoaffinity MS approach. The expected β-catenin peptides and a set of 38 epitope-containing peptides were identified from trypsin-digested cell lysates. This might be a first step in the development of proteomics applications that are based on the use of peptide class-specific antibodies.
Highlights
From the ‡NMI Natural and Medical Sciences Institute at the University of Tubingen, Markwiesenstrasse 55, 72770 Reutlingen, Germany, ¶Centre for Bioinformatics, University of Tubingen, Sand 14, 72076 Tubingen, Germany, and ʈUniversity of Applied Sciences Albstadt-Sigmaringen, Anton-Gunther-Strasse 51, 72488 Sigmaringen, Germany
Triple X Proteomics Concept—The use of peptide-specific antibodies that recognize peptide fragments generated by the enzymatic digestion of a proteome is an effective method for enriching target peptides from highly complex samples
Combined with Mass spectrometry (MS) analysis, it is a valuable tool for targeted proteomics
Summary
Antigens were generated by conjugating the peptides to keyhole limpet hemocyanin (KLH). KLH (Pierce) was reconstituted in sterile double distilled H2O to a concentration of 10 mg/ml. Sulfo-m-maleimidobenzoyl-N-hydroxysuccinimide ester (sMBS; Pierce) was freshly dissolved in DMSO at a concentration of 40 mg/ml. 1 volume of sMBS solution was mixed with 10 volumes of KLH solution and incubated at room temperature (RT) for 1 h on an orbital shaker. Cysteine-containing peptide antigens were dissolved in PBS at a concentration of 4 mg/ml. The peptides were mixed 1:1 (w/w) with the preactivated KLH and gently mixed for 3 h at RT. Rabbits were immunized with these conjugates at Pineda Antibody Service, Berlin, Germany, and sacrificed after day 81 to obtain polyclonal serum. The peptides were purchased from Intavis, Reutlingen, Germany
Published Version (Free)
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.