Intensity-fading MALDI-TOF-MS: Novel screening for ligand binding and drug discovery Journal Article


Authors: Yanes, Ó; Villanueva, J.; Querol, E.; Aviles, F. X.
Article Title: Intensity-fading MALDI-TOF-MS: Novel screening for ligand binding and drug discovery
Abstract: Ligand discovery technologies largely rely on a primary screening for molecules showing affinity to a target, coupled with an approach to identify these molecules. Matrix-assisted laser desorption ionization (MALDI) time-of-flight (TOF) mass spectrometry (MS) is attracting increasing attention as a suitable analytical technique for ligand identification owing to its high sensitivity and capacity for discrimination, its fast analysis and its ease of automation. There is now a range of related strategies for drug discovery, including a novel MS-based methodology to screen noncovalent interactions between macromolecular targets (proteases) and peptide or organic ligands (protease inhibitors) called intensity-fading (IF) MALDI-TOF-MS. © 2004 Elsevier Ltd. All rights reserved.
Keywords: review; nonhuman; drug targeting; binding affinity; accuracy; protein analysis; protein targeting; drug screening; peptide; automation; drug research; capillary electrophoresis; matrix assisted laser desorption ionization time of flight mass spectrometry; surface plasmon resonance; proteinase inhibitor; ligand binding; protein cross linking; protein immobilization; affinity chromatography; gel permeation chromatography
Journal Title: Drug Discovery Today: TARGETS
Volume: 3
Issue: 2 Suppl.
ISSN: 1741-8372
Publisher: Elsevier Inc.  
Date Published: 2004-04-01
Start Page: S23
End Page: S30
Language: English
PROVIDER: scopus
DOI: 10.1016/S1741-8372(04)02417-X
DOI/URL:
Notes: Drug Discov. Today Targets -- Cited By (since 1996):8 -- Export Date: 16 June 2014 -- CODEN: DDTTA -- Source: Scopus
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