Detection of non-covalent protein interactions by 'intensity fading' MALDI-TOF mass spectrometry: Applications to proteases and protease inhibitors Journal Article


Authors: Yanes, O.; Villanueva, J.; Querol, E.; Aviles, F. X.
Article Title: Detection of non-covalent protein interactions by 'intensity fading' MALDI-TOF mass spectrometry: Applications to proteases and protease inhibitors
Abstract: Among the main objectives of biomedical and proteomic research is to identify non-covalent interactions involving proteins. Here we provide a detailed protocol to apply matrix-assisted laser desorption ionization (MALDI) time-of-flight (TOF) mass spectrometry for such a purpose using proteases and protease inhibitors in complex biological samples. Our methodology is based on monitoring the reduction in intensity of inhibitors' mass spectrometric signals when their protease target is added to the MALDI sample. The versatility of the protocol permits the target to be added in a soluble form (direct protocol) or immobilized form (indirect protocol). The 'intensity fading' phenomenon is greatly favored when the binding assay is carried out in the sub-micromolar range and the interacting partners occur in mixtures of non-binding compounds. This protocol can be completed in 10 h, taking 20 or 30 min per sample to perform the mass spectrometric data acquisition, depending on whether a soluble or an immobilized target is used.
Keywords: controlled study; methodology; mass spectrometry; aprotinin; metabolism; protease inhibitors; protein targeting; protein interaction; information processing; proteomics; time; chemistry; serine proteinase; proteinase; matrix assisted laser desorption ionization time of flight mass spectrometry; signal processing; proteinase inhibitor; peptide hydrolases; peptide hydrolase; spectrometry, mass, matrix-assisted laser desorption-ionization; biomedicine; binding assay; reversed phase high performance liquid chromatography; n [n (3 carboxyoxirane 2 carbonyl)leucyl]agmatine; papain; process monitoring
Journal Title: Nature Protocols
Volume: 2
Issue: 1
ISSN: 1754-2189
Publisher: Nature Publishing Group  
Date Published: 2007-02-01
Start Page: 119
End Page: 130
Language: English
DOI: 10.1038/nprot.2006.487
PUBMED: 17401346
PROVIDER: scopus
DOI/URL:
Notes: --- - "Cited By (since 1996): 11" - "Export Date: 17 November 2011" - "Source: Scopus"
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