Journal article

Affinity mass spectrometry-based approaches for the analysis of protein-protein interaction and complex mixtures of peptide-ligands


Authors listRüdiger, AH; Rüdiger, M; Carl, UD; Chakraborty, T; Roepstorff, P; Wehland, J

Publication year1999

Pages162-170

JournalAnalytical Biochemistry

Volume number275

Issue number2

ISSN0003-2697

DOI Linkhttps://doi.org/10.1006/abio.1999.4319

PublisherElsevier


Abstract
Combined applications of affinity purification procedures and mass-spectrometric analyses (affinity mass spectrometry or affinity-directed mass spectrometry) have gained broad interest in various fields of biological sciences. We have extended these techniques to the purification and analysis of closely related peptides from complex mixtures and to the characterization of binding motifs and relative affinities in protein-protein interactions. The posttranslational modifications in the carboxy-terminal region of porcine brain tubulin are used as an example for the applicability of affinity mass spectrometry in the characterization of complex patterns of related peptides. We also show that affinity mass spectrometry allows the mapping of sequential binding motifs of two interacting proteins. Using the ActA/Mena protein-protein complex as a model system, we show that we can selectively purify Mena-binding peptides from a tryptic digest of ActA. The results from this assay are compared to data sets obtained earlier by classical methods using synthetic peptides and molecular genetic experiments. As a further expansion of affinity mass spectrometry, we have established an internally standardized system that allows comparison of the affinities of related ligands for a given protein. Here the affinities of two peptide ligands for the monoclonal tubulin-specific antibody YL1/2 are determined in terms of half-maximal competition. (C) 1999 Academic Press.



Citation Styles

Harvard Citation styleRüdiger, A., Rüdiger, M., Carl, U., Chakraborty, T., Roepstorff, P. and Wehland, J. (1999) Affinity mass spectrometry-based approaches for the analysis of protein-protein interaction and complex mixtures of peptide-ligands, Analytical Biochemistry, 275(2), pp. 162-170. https://doi.org/10.1006/abio.1999.4319

APA Citation styleRüdiger, A., Rüdiger, M., Carl, U., Chakraborty, T., Roepstorff, P., & Wehland, J. (1999). Affinity mass spectrometry-based approaches for the analysis of protein-protein interaction and complex mixtures of peptide-ligands. Analytical Biochemistry. 275(2), 162-170. https://doi.org/10.1006/abio.1999.4319



Keywords


affinity mass spectrometryALPHA-TUBULINBIOMOLECULAR INTERACTION ANALYSISEPITOPELISTERIA-MONOCYTOGENESMALDI-TOF-MSmixtures of ligandsMONOCLONAL-ANTIBODYPROBE

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