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1.
J Mass Spectrom ; 47(6): 786-94, 2012 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-22707171

RESUMO

The fragmentation behavior of the 2+ and 3+ charge states of eleven different phosphorylated tau peptides was studied using collision-induced dissociation (CID), electron transfer dissociation (ETD) and metastable atom-activated dissociation (MAD). The synthetic peptides studied contain up to two known phosphorylation sites on serine or threonine residues, at least two basic residues, and between four and eight potential sites of phosphorylation. CID produced mainly b-/y-type ions with abundant neutral losses of the phosphorylation modification. ETD produced c-/z-type ions in highest abundance but also showed numerous y-type ions at a frequency about 50% that of the z-type ions. The major peaks observed in the ETD spectra correspond to the charge-reduced product ions and small neutral losses from the charge-reduced peaks. ETD of the 2+ charge state of each peptide generally produced fewer backbone cleavages than the 3+ charge state, consistent with previous reports. Regardless of charge state, MAD achieved more extensive backbone cleavage than CID or ETD, while retaining the modification(s) in most cases. In all but one case, unambiguous modification site determination was achieved with MAD. MAD produced 15-20% better sequence coverage than CID and ETD for both the 2+ and 3+ charge states and very different fragmentation products indicating that the mechanism of fragmentation in MAD is unique and complementary to CID and ETD.


Assuntos
Espectrometria de Massas/métodos , Fosfopeptídeos/química , Análise de Sequência de DNA/métodos , Proteínas tau/química , Sequência de Aminoácidos , Íons/química , Dados de Sequência Molecular
2.
Talanta ; 83(4): 1260-8, 2011 Jan 30.
Artigo em Inglês | MEDLINE | ID: mdl-21215862

RESUMO

A fast method that can be used to classify unknown jet fuel types or detect possible property changes in jet fuel physical properties is of paramount interest to national defense and the airline industries. While fast gas chromatography (GC) has been used with conventional mass spectrometry (MS) to study jet fuels, fast GC was combined with fast scanning MS and used to classify jet fuels into lot numbers or origin for the first time by using fuzzy rule-building expert system (FuRES) classifiers. In the process of building classifiers, the data were pretreated with and without wavelet transformation and evaluated with respect to performance. Principal component transformation was used to compress the two-way data images prior to classification. Jet fuel samples were successfully classified with 99.8 ± 0.5% accuracy for both with and without wavelet compression. Ten bootstrapped Latin partitions were used to validate the generalized prediction accuracy. Optimized partial least squares (o-PLS) regression results were used as positively biased references for comparing the FuRES prediction results. The prediction results for the jet fuel samples obtained with these two methods were compared statistically. The projected difference resolution (PDR) method was also used to evaluate the fast GC and fast MS data. Two batches of aliquots of ten new samples were prepared and run independently 4 days apart to evaluate the robustness of the method. The only change in classification parameters was the use of polynomial retention time alignment to correct for drift that occurred during the 4-day span of the two collections. FuRES achieved perfect classifications for four models of uncompressed three-way data. This fast GC/fast MS method furnishes characteristics of high speed, accuracy, and robustness. This mode of measurement may be useful as a monitoring tool to track changes in the chemical composition of fuels that may also lead to property changes.


Assuntos
Classificação/métodos , Sistemas Inteligentes , Lógica Fuzzy , Cromatografia Gasosa-Espectrometria de Massas/métodos , Hidrocarbonetos/classificação , Meios de Transporte , Análise por Conglomerados , Cromatografia Gasosa-Espectrometria de Massas/instrumentação , Hidrocarbonetos/análise , Análise dos Mínimos Quadrados , Análise de Componente Principal , Reprodutibilidade dos Testes , Fatores de Tempo
3.
Ther Drug Monit ; 32(2): 216-23, 2010 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-20216108

RESUMO

We present the development of a new, faster analytical method for the determination of fatty acid ethyl esters (FAEEs) in human hair to detect potential alcohol abuse. FAEEs have been established as metabolites of ethanol consumption in humans and are embedded in the hair follicles during hair growth. The developed method has a total analysis time-including washing, extraction, concentration, separation, and detection-of less than 1 hour. Commonly used extraction procedures in the literature for these biomarkers are typically 15 hours. Analysis is performed using gas chromatography-tandem mass spectrometry (GC-MS/MS) with a GC separation time of less than 9 minutes. Using chemical ionization, mass spectrometric detection consists of selected reaction monitoring, which is widely considered to be one of the most selective and sensitive forms of mass spectrometric detection. Employing selected reaction monitoring helps to reduce interferences from the hair matrix, thereby making the method more selective for these biomarkers of interest. Limits of detection for each FAEE range from 0.002 to 0.030 ng/mg in hair. By using this faster extraction method, this research shows that this method could potentially be used to distinguish whether a person is a heavy drinker, moderate drinker, or nondrinker. The ability to rapidly analyze hair samples can be applied to a number of different areas, such as neonatal screening, parole violations, contributing factors in the cause of death, and any other application requiring the establishment of chronic versus acute alcohol abuse.


Assuntos
Consumo de Bebidas Alcoólicas/metabolismo , Alcoolismo/diagnóstico , Cromatografia Gasosa-Espectrometria de Massas/normas , Cabelo/química , Detecção do Abuso de Substâncias/normas , Alcoolismo/metabolismo , Biomarcadores/análise , Biomarcadores/metabolismo , Cromatografia Gasosa-Espectrometria de Massas/métodos , Cabelo/metabolismo , Humanos , Detecção do Abuso de Substâncias/métodos , Temperança
4.
J Forensic Sci ; 53(6): 1437-42, 2008 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-18717751

RESUMO

This paper describes the sequence of analyses used to determine the nature of a stain located on the floor of room in the former Athens Mental Health and Retardation Hospital in Athens, OH. The location of the stain was reported to be the position in which a decomposing body was discovered on January 11, 1979. The current stain is found to contain strong evidence for both natural decomposition products and deliberate adulteration. Microscopic analyses, solubility tests, FTIR, ICP-OES, pyrolysis-MS, and derivatization GC-MS were consistent in determining the removable parts of the stain to be composed mostly of calcium and sodium salts of free fatty acids, such as palmitic acid, consistent with previous descriptions of adipocere. The free fatty acids could have been formed via known bacterial degradation pathways or via saponification through the basic environment caused through contact with the concrete. To our knowledge, adipocere formation on an exposed indoor environment has not been described before. The stain and concrete also show signs of being chemically modified with an acidic reagent, such as Blu-Lite--a phosphoric acid-based cleaner that was a commonly used cleaner in the building from the time of discovery to the present day. The chemical etching appears to have been restricted to an area resembling the shape of a human body, which is consistent with deliberate adulteration of the appearance of the stain.


Assuntos
Materiais de Construção , Ácidos Graxos não Esterificados/análise , Pisos e Cobertura de Pisos , Mudanças Depois da Morte , Cálcio/análise , Detergentes , Feminino , Patologia Legal , Cromatografia Gasosa-Espectrometria de Massas , Humanos , Espectrometria de Massas , Microscopia , Pessoa de Meia-Idade , Sódio/análise , Análise Espectral
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