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1.
Int J Mol Sci ; 24(24)2023 Dec 05.
Artículo en Inglés | MEDLINE | ID: mdl-38138989

RESUMEN

Regulatory adenine nucleotide-binding cystathionine ß-synthase (CBS) domains are widespread in proteins; however, information on the mechanism of their modulating effects on protein function is scarce. The difficulty in obtaining structural data for such proteins is ascribed to their unusual flexibility and propensity to form higher-order oligomeric structures. In this study, we deleted the most movable domain from the catalytic part of a CBS domain-containing bacterial inorganic pyrophosphatase (CBS-PPase) and characterized the deletion variant both structurally and functionally. The truncated CBS-PPase was inactive but retained the homotetrameric structure of the full-size enzyme and its ability to bind a fluorescent AMP analog (inhibitor) and diadenosine tetraphosphate (activator) with the same or greater affinity. The deletion stabilized the protein structure against thermal unfolding, suggesting that the deleted domain destabilizes the structure in the full-size protein. A "linear" 3D structure with an unusual type of domain swapping predicted for the truncated CBS-PPase by Alphafold2 was confirmed by single-particle electron microscopy. The results suggest a dual role for the CBS domains in CBS-PPase regulation: they allow for enzyme tetramerization, which impedes the motion of one catalytic domain, and bind adenine nucleotides to mitigate or aggravate this effect.


Asunto(s)
Cistationina betasintasa , Pirofosfatasas , Pirofosfatasas/metabolismo , Cistationina betasintasa/genética , Cistationina betasintasa/metabolismo , Dominio Catalítico , Proteínas Bacterianas/metabolismo , Nucleótidos
2.
Biochim Biophys Acta Gen Subj ; 1865(1): 129762, 2021 01.
Artículo en Inglés | MEDLINE | ID: mdl-33053413

RESUMEN

BACKGROUND: Previous studies have demonstrated the formation of stable complexes between inorganic pyrophosphatase (PPase) and three other Escherichia coli enzymes - cupin-type phosphoglucose isomerase (cPGI), class I fructose-1,6-bisphosphate aldolase (FbaB) and l-glutamate decarboxylase (GadA). METHODS: Here, we determined by activity measurements how complex formation between these enzymes affects their activities and oligomeric structure. RESULTS: cPGI activity was modulated by all partner proteins, but none was reciprocally affected by cPGI. PPase activity was down-regulated upon complex formation, whereas all other enzymes were up-regulated. For cPGI, the activation was partially counteracted by a shift in dimer ⇆ hexamer equilibrium to inactive hexamer. Complex stoichiometry appeared to be 1:1 in most cases, but FbaB formed both 1:1 and 1:2 complexes with both GadA and PPase, FbaB activation was only observed in the 1:2 complexes. FbaB and GadA induced functional asymmetry (negative kinetic cooperativity) in hexameric PPase, presumably by favoring partial dissociation to trimers. CONCLUSIONS: These four enzymes form all six possible binary complexes in vitro, resulting in modulated activity of at least one of the constituent enzymes. In five complexes, the effects on activity were unidirectional, and in one complex (FbaB⋅PPase), the effects were reciprocal. The effects of potential physiological significance include inhibition of PPase by FbaB and GadA and activation of FbaB and cPGI by PPase. Together, they provide a mechanism for feedback regulation of FbaB and GadA biosynthesis. GENERAL SIGNIFICANCE: These findings indicate the complexity of functionally significant interactions between cellular enzymes, which classical enzymology treats as individual entities, and demonstrate their moonlighting activities as regulators.


Asunto(s)
Proteínas de Escherichia coli/metabolismo , Escherichia coli/metabolismo , Fructosa-Bifosfato Aldolasa/metabolismo , Glucosa-6-Fosfato Isomerasa/metabolismo , Glutamato Descarboxilasa/metabolismo , Pirofosfatasa Inorgánica/metabolismo , Proteínas de la Membrana/metabolismo , Escherichia coli/química , Infecciones por Escherichia coli/microbiología , Proteínas de Escherichia coli/química , Fructosa-Bifosfato Aldolasa/química , Glucosa-6-Fosfato Isomerasa/química , Glutamato Descarboxilasa/química , Humanos , Pirofosfatasa Inorgánica/química , Cinética , Proteínas de la Membrana/química , Multimerización de Proteína
3.
PLoS One ; 11(5): e0156105, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27227414

RESUMEN

The structural analyses of four metabolic enzymes that maintain and regulate the stationary growth phase of Escherichia coli have been performed primarily drawing on the results obtained from solution small angle X-ray scattering (SAXS) and other structural techniques. The proteins are (i) class I fructose-1,6-bisphosphate aldolase (FbaB); (ii) inorganic pyrophosphatase (PPase); (iii) 5-keto-4-deoxyuronate isomerase (KduI); and (iv) glutamate decarboxylase (GadA). The enzyme FbaB, that until now had an unknown structure, is predicted to fold into a TIM-barrel motif that form globular protomers which SAXS experiments show associate into decameric assemblies. In agreement with previously reported crystal structures, PPase forms hexamers in solution that are similar to the previously reported X-ray crystal structure. Both KduI and GadA that are responsible for carbohydrate (pectin) metabolism and acid stress responses, respectively, form polydisperse mixtures consisting of different oligomeric states. Overall the SAXS experiments yield additional insights into shape and organization of these metabolic enzymes and further demonstrate the utility of hybrid methods, i.e., solution SAXS combined with X-ray crystallography, bioinformatics and predictive 3D-structural modeling, as tools to enrich structural studies. The results highlight the structural complexity that the protein components of metabolic networks may adopt which cannot be fully captured using individual structural biology techniques.


Asunto(s)
Isomerasas Aldosa-Cetosa/química , Escherichia coli/enzimología , Fructosa-Bifosfato Aldolasa/química , Glutamato Descarboxilasa/química , Pirofosfatasa Inorgánica/química , Dispersión del Ángulo Pequeño , Difracción de Rayos X/métodos , Isomerasas Aldosa-Cetosa/metabolismo , Biología Computacional , Fructosa-Bifosfato Aldolasa/metabolismo , Glutamato Descarboxilasa/metabolismo , Pirofosfatasa Inorgánica/metabolismo , Modelos Moleculares , Conformación Proteica , Soluciones
4.
Wien Klin Wochenschr ; 114(13-14): 610-2, 2002 Jul 31.
Artículo en Inglés | MEDLINE | ID: mdl-12422610

RESUMEN

A clinical-laboratory survey of 1952 patients with acute feverish diseases developing after tick bite was carried out in the Pre-Ural region of Russia, which is endemic for tick-borne encephalitis and ixodid tick-borne borreliosis, in 1999-2001. Enzyme-linked immunosorbent assay and indirect immunofluorescence assay were used for the detection of tick-borne encephalitis, ixodid tick-borne borreliosis and ehrlichiosis specific antibodies. Tick-borne encephalitis was diagnosed in 22.8% of patients, ixodid tick-borne borreliosis in 50.5%, ehrlichiosis in 4.5% and mixed infections in 2.9%. For the first time in Russia, a new transmitted disease that appeared to be human monocytic ehrlichiosis was identified and its clinical manifestations were described. The common feature of these infections is the acute course and the marked general infectious syndrome at the early period of the disease. Disorders of the nervous system predominate in tick-borne encephalitis. In ixodid tick-borne borreliosis the development of erythema migrans and organic pathology (disorders of the cardio-vascular system and liver) associated with the involvement of the nervous and locomotor system are pathognomonically significant. The specific characteristics of human monocytic ehrlichiosis include nervous impairments, hepatic lesions, the frequent development of a two-wave course and hemogram changes.


Asunto(s)
Enfermedades Endémicas , Enfermedades por Picaduras de Garrapatas/diagnóstico , Enfermedad Aguda , Animales , Mordeduras y Picaduras/complicaciones , Estudios Transversales , Ehrlichiosis/diagnóstico , Ehrlichiosis/epidemiología , Ehrlichiosis/transmisión , Encefalitis Transmitida por Garrapatas/diagnóstico , Encefalitis Transmitida por Garrapatas/epidemiología , Encefalitis Transmitida por Garrapatas/transmisión , Eritema Crónico Migrans/diagnóstico , Eritema Crónico Migrans/epidemiología , Eritema Crónico Migrans/transmisión , Humanos , Ixodes , Enfermedad de Lyme/diagnóstico , Enfermedad de Lyme/epidemiología , Enfermedad de Lyme/transmisión , Federación de Rusia/epidemiología , Enfermedades por Picaduras de Garrapatas/epidemiología , Enfermedades por Picaduras de Garrapatas/transmisión
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