Journalartikel

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


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

Jahr der Veröffentlichung1999

Seiten162-170

ZeitschriftAnalytical Biochemistry

Bandnummer275

Heftnummer2

ISSN0003-2697

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

VerlagElsevier


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.



Zitierstile

Harvard-ZitierstilRüdiger, 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-ZitierstilRüdiger, 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



Schlagwörter


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


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