Matrix-assisted laser desorption/ionization (MALDI) mass spectra were obtained from single biological aerosol particles using an aerosol time-of-flight mass spectrometer (ATOFMS). The inlet to the ATOFMS was coupled with an evaporation/condensation flow cell that allowed the aerosol to be coated wit
A Method for Application of Samples to Matrix-Assisted Laser Desorption Ionization Time-of-Flight Targets That Enhances Peptide Detection
β Scribed by France Landry; Christian R. Lombardo; Jeffrey W. Smith
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 268 KB
- Volume
- 279
- Category
- Article
- ISSN
- 0003-2697
No coin nor oath required. For personal study only.
β¦ Synopsis
Matrix-assisted laser desorption ionization time-offlight (MALDI-TOF) mass spectrometry has become a fundamental tool for the identification and analysis of peptides and proteins. MALDI-TOF is well suited for the analysis of complex biological mixtures because samples are crystallized onto a solid support that can be washed to remove contaminants and salts prior to laser desorption. A number of approaches for immobilizing samples onto MALDI targets have been put forth. These include the use of different chemical matrices and the immobilization of samples onto different solid supports. In large part though, the preparation of MALDI targets has been an empirical exercise that often requires a unique series of conditions for every sample. Here, a simple method for the application of peptide mixtures onto MALDI targets is put forth. This method differs because peptides are added directly to a sample of nitrocellulose dissolved in acetone, allowing them to interact in solution-phase organic solvent. This solution-phase mixture is then spotted to the MALDI target and evaporated, forming a homogenous solid surface for laser desorption. This procedure is robust, highly sensitive, tolerant to detergents, and easily learned. In our hands, the method provides as much as a 10-fold enhancement to the detection of tryptic peptide fragments derived from ingel digests.
π SIMILAR VOLUMES
Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) has been used as a rapid method for the detection of human genetic polymorphisms. In particular, the mutations in the human HEXA gene that cause the infantile Tay-Sachs disease have been studied using MALDI-MS to demonstrate th
## Abstract The circuit shape of the ion path, or the multiβturn, provides a solution for achieving unrestricted mass resolution from timeβofβflight mass analyzers. The potential of a multiβturn type mass spectrometer, the MULTUM II, with a 1.308 m circuit controlled by four toroidal electric secto
for a good recovery, whereas no effect was observed from protease inhibitors. No detectable loss was observed in the lyophilized product. In a subsequent experiment, the stability of alb-OC was analyzed under optimal conditions for prolonged periods of time. Storage conditions for the diluted produc
Two methods for the collection of capillary electrophoresis fractions for analysis by matrix-assisted laser desorption/ionization have been investigated; the first using a novel ion-porous joint design for dropwise fraction collection and the second, a process of electrospray deposition. Sensitivity
analyst is faced with a mixture of carbohydrate struc-On-the-probe sample cleanup strategies were develtures to characterize given most glycosylation sites exoped for matrix-assisted laser desorption-ionization hibit structural microheterogenetity (1). Direct analy-(MALDI) time-of-flight mass spectr