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1.
Clin Chim Acta ; 492: 102-113, 2019 May.
Artículo en Inglés | MEDLINE | ID: mdl-30776362

RESUMEN

BACKGROUND: Type II Congenital Disorders of Glycosylation (CDG-II) are a group of diseases with challenging diagnostics characterized by defects in the processing of glycans in the Golgi apparatus. Mass Spectrometry (MS) has been a valuable tool in the definition of CDG-II subtypes. While some CDG-II subtypes are associated with specific N-glycan structures, others only produce changes in relative levels, reinforcing the demand for quantification methods. METHODS: Plasma samples from control individuals were pooled, derivatized with deuterated iodomethane (I-CD3), and used as internal standards for controls and patients whose glycans were derivatized with iodomethane (I-CH3), followed by MALDI MS, LC-MS and -MS/MS analyses. RESULTS: Total N-glycans from fifteen CDG-II patients were evaluated, and 4 cases with molecular diagnosis were considered in detail: 2ATP6V0A2-CDG siblings, and 2 MAN1B1-CDG patients, one of them carrying a previously undescribed p.Gly536Val mutation. CONCLUSIONS: Our methodology offers a feasible alternative to the current methods for CDG-II diagnosis by MS, which quantify glycan structures as fractions of the total summed signal across a mass spectrum, a strategy that lowers the variability of minor components. Moreover, given its sensitivity for less concentrated yet biologically relevant structures, it might assist the uncovering of novel diagnostic glycans in other CDG-II subtypes.


Asunto(s)
Análisis Químico de la Sangre/métodos , Trastornos Congénitos de Glicosilación/sangre , Polisacáridos/sangre , Espectrometría de Masa por Láser de Matriz Asistida de Ionización Desorción/métodos , Adolescente , Niño , Preescolar , Trastornos Congénitos de Glicosilación/genética , Femenino , Genotipo , Humanos , Lactante , Masculino , Mutación
2.
Biochim Biophys Acta ; 1383(1): 165-74, 1998 Mar 03.
Artículo en Inglés | MEDLINE | ID: mdl-9546058

RESUMEN

We studied the effect of pressure up to 300 bar on the catalytic efficiency of subtilisin Carlsberg suspended in compressed propane, near-critical ethane, near-critical carbon dioxide and tert-amyl alcohol, at constant temperature and fixed enzyme hydration. Increasing pressure lowered the catalytic efficiency of the enzyme in all the solvents, resulting in positive activation volumes, delta V#. The delta V# values in compressed propane and in tert-amyl alcohol were similar and larger in magnitude than the value reported in the literature for the same reaction in an aqueous buffer, although within the range of typical delta V# values in aqueous media. In the near-critical fluids, the delta V# were much larger, e.g., an increase in pressure of only 200 bar causing a sixfold decrease in the catalytic efficiency of subtilisin in carbon dioxide. These data should reflect the proximity of ethane and carbon dioxide to the critical point, and the resulting condensation of solvent molecules about the solutes, yielding negative solute partial molar volumes.


Asunto(s)
Dióxido de Carbono , Etano , Propano , Subtilisinas/química , Catálisis , Modelos Logísticos , Pentanoles , Presión
3.
Biotechnol Prog ; 17(2): 355-8, 2001.
Artículo en Inglés | MEDLINE | ID: mdl-11312714

RESUMEN

We report on the performance of cross-linked enzyme microcrystals (CLECs) of subtilisin Carlsberg in supercritical fluids (SC-fluids). The catalytic activity of CLECs in SC-ethane was found to be 2- to 10-fold greater than in hexane under the same conditions, using CLECs dried by propanol washing. Air-dried CLECs and lyophilized powders showed much lower activities, reflecting the same hydration hysteresis effects as in organic solvents. Reaction rates were much lower in SC-CO(2), especially at higher water activity, probably as a result of acid-base effects of carbonic acid on the enzyme.


Asunto(s)
Subtilisinas/metabolismo , Catálisis , Cristalización , Esterificación , Cinética , Subtilisinas/química
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