RESUMEN
Differential diagnosis of bacterial and viral meningitis is an urgent problem of the modern clinical medicine. Early and accurate detection of meningitis etiology largely determines the strategy of its treatment and significantly increases the likelihood of a favorable outcome for the patient. In the present work, we analyzed the peptidome and cytokine profiles of cerebrospinal fluid (CSF) of 17 patients with meningitis of bacterial and viral etiology and of 20 neurologically healthy controls. In addition to the identified peptides (potential biomarkers), we found significant differences in the cytokine status of the CSF of the patients. We found that cut-off of 100 pg/ml of IL-1ß, TNF, and GM-CSF levels discriminates bacterial and viral meningitis with 100% specificity and selectivity. We demonstrated for the first time the reduction in the level of two cytokines, IL-13 and GM-CSF, in the CSF of patients with viral meningitis in comparison with the controls. The decrease in GM-CSF level in the CSF of patients with viral meningitis can be explained by a disproportionate increase in the levels of cytokines IL-10, IFN-γ, and IL-4, which inhibit the GM-CSF expression, whereas IL-1, IL-6, and TNF activate it. These observations suggest an additional approach for differential diagnosis of bacterial and viral meningitis based on the normalized ratio IL-10/IL-1ß and IL-10/TNF > 1, as well as on the ratio IFN-γ/IL-1ß and IFN-γ/TNF < 0.1. Our findings extend the panel of promising clinical and diagnostic biomarkers of viral and bacterial meningitis and reveal opposite changes in the cytokine expression in meningitis due to compensatory action of pro- and antiinflammatory factors.
Asunto(s)
Citocinas/líquido cefalorraquídeo , Mediadores de Inflamación/líquido cefalorraquídeo , Meningitis Bacterianas/líquido cefalorraquídeo , Meningitis Viral/líquido cefalorraquídeo , Adulto , Anciano , Anciano de 80 o más Años , Biomarcadores/líquido cefalorraquídeo , Citocinas/inmunología , Femenino , Humanos , Mediadores de Inflamación/inmunología , Masculino , Meningitis Bacterianas/inmunología , Meningitis Viral/inmunología , Persona de Mediana EdadRESUMEN
The bacterial cell wall muramyl dipeptides MDP and glucosaminyl-MDP (GMDP) are powerful immunostimulators but their binding target remains controversial. We previously reported expression cloning of GMDP-binding polypeptides and identification of Y-box protein 1 (YB-1) as their sole target. Here we show specific binding of GMDP to recombinant YB-1 protein and subcellular colocalization of YB-1 and GMDP. GMDP binding to YB-1 upregulated gene expression levels of NF-κB2, a mediator of innate immunity. Furthermore, YB-1 knockdown abolished GMDP-induced Nfkb2 expression. GMDP/YB-1 stimulation led to NF-κB2 cleavage, transport of activated NF-κB2 p52 to the nucleus, and upregulation of NF-κB2-dependent chemokine Cxcr4 gene expression. Therefore, our findings identify YB-1 as new target for muramyl peptide signaling.
Asunto(s)
Acetilmuramil-Alanil-Isoglutamina/análogos & derivados , Bacterias/metabolismo , Pared Celular/metabolismo , Inmunidad Innata , Proteína 1 de Unión a la Caja Y/metabolismo , Acetilmuramil-Alanil-Isoglutamina/metabolismo , Animales , Secuencia de Bases , Sitios de Unión , Células Cultivadas , Cartilla de ADN , RatonesRESUMEN
16 DSIP analogues with substitutions of 1-2 amino acid residues were synthesized in order to investigate their potential use in medicine. Antioxidative properties of these peptides were studied in vitro and their detoxifying activity was examined in vivo on a model of toxicosis that was induced by the cisplatin cytostatic, which has been widely used in the cancer treatment. Practically all the studied DSIP analogues were shown to exhibit considerable direct antioxidative activity (AOA), and that of the ID-6 analogue was higher than AOA of DSIP and comparable with AOA of vitamin C and ß-carotine. This analogue also demonstrated the most pronounced detoxifying effect towards cisplatin action, resulting in a decrease in the animal death from the acute cisplatin toxicity to 17% (in comparison with 50-67% for the control animals) and restoration of a number of cisplatin-sensitive biochemical blood parameters: decrease in the activity of aspartate aminotransferase and alanine aminotransferase and downregulation of the concentration of the final products of nitrogen exchange (creatinine and urea). Thus, the DSIP-relative peptides could be promising agents for the decrease in the toxic effects of cytostatics that are used in oncology.
Asunto(s)
Antioxidantes/farmacología , Cisplatino/efectos adversos , Péptido Inductor del Sueño Delta/análogos & derivados , Neuropéptidos/farmacología , Sustitución de Aminoácidos , Animales , Antioxidantes/química , Ácido Ascórbico/farmacología , Cisplatino/toxicidad , Femenino , Inactivación Metabólica/efectos de los fármacos , Peroxidación de Lípido/efectos de los fármacos , Ratones Endogámicos , Neuropéptidos/síntesis química , Neuropéptidos/química , Técnicas de Síntesis en Fase Sólida , Relación Estructura-Actividad , beta Caroteno/farmacologíaRESUMEN
We have undertaken a comparative study on physiological activity of well known neuropeptide DSIP (WAGGDASG E) and new closely related peptide KND (WKGGNASGE) in vivo assays. The sequence of K2, N5-DSIP (KND) was found recently by the computer search for DSIP homologous sequences in available nucleotide and protein databases at 324-332 site of Lysine-specific demethylase 3 B (EC 1.14.11, Swiss-Prot: Q7LBC6.1, 1-1761aa). This human lysine-specific histone demethylase is a representative of the recently discovered family of so called JmjC-domain-containing histone demethylases encoded by JMJD1B gene and ubiquitously expressed in tissues of various mammalian species. Biological investigations performed in this work confirm our preliminary data that DSIP-related peptide KND exhibits the similar biological properties in comparison with DSIP. Assessed by us antioxidative, anticonvulsive and behavioral effects of KND were even more expressed than in DSIP case. These results provide the additional evidences to support our suggestion that KND can be a possible endogenous prototype of "real" DSIP.
Asunto(s)
Conducta Animal/efectos de los fármacos , Péptido Inductor del Sueño Delta/administración & dosificación , Histona Demetilasas con Dominio de Jumonji/metabolismo , Péptidos/administración & dosificación , Altitud , Animales , Antioxidantes/administración & dosificación , Péptido Inductor del Sueño Delta/química , Humanos , Hipoxia/tratamiento farmacológico , Hipoxia/patología , Histona Demetilasas con Dominio de Jumonji/genética , Peroxidación de Lípido/efectos de los fármacos , Pentilenotetrazol/toxicidad , Péptidos/química , Péptidos/metabolismo , Ratas , Convulsiones/inducido químicamente , Convulsiones/tratamiento farmacológico , Convulsiones/patologíaRESUMEN
Synthetic peptides corresponding to the 59-72 (I), 60-72 (II) and 61-72 (III) sequences of human interleukin 2 with their N(alpha) acetylated and C(alpha) methylated termini were shown to exhibit pronounced hepatoprotective properties. These peptides neutralized hepatotoxic effects of such agents as tetrachloromethane and galactosamine in experiments in vivo. The peptide action revealed as normalization of duration of the thiopental narcosis of experimental animals and the level of hepatospecific enzymes in their blood. The effects of peptides (I)-(III) proved to be similar to that of prednisolone (the well-known anti-inflammatory agent), whereas the bestatine cytotoxic dipeptide had no hepatoprotecting effect. The target of the hepatoprotective activity of the peptides was shown to be the preliminary activated macrophages. We proposed that this activity of the peptides was associated with their interaction with the a-subunit of the interleukin 2 receptor (IL-2Ralpha), because the X-Ray analysis pointed to this region as one of binding sites of IL-2 with IL-2Ralpha. Experiments on the influence of the most active (59-72)-peptide on growth of the IL-2 dependent cell line (CTLL) confirmed this proposal. The 3H-labeled peptide corresponding to the 59-72 sequence ofthe human IL-2 was shown to bind to the CTLL cels. We assumed that the binding of this peptide was specific and occurred precisely with IL-2Ra and virtually determined the binding constant. Its value (1.41 x 10(-6) M) was comparable with that of the interaction of IL-2 with IL-2Ralpha (approximately 10(-7) M).
Asunto(s)
Subunidad alfa del Receptor de Interleucina-2 , Interleucina-2 , Fragmentos de Péptidos , Sustancias Protectoras , Animales , Sitios de Unión , Tetracloruro de Carbono/toxicidad , Línea Celular , Proliferación Celular/efectos de los fármacos , Galactosamina/toxicidad , Hepatocitos/citología , Hepatocitos/efectos de los fármacos , Hepatocitos/enzimología , Humanos , Interleucina-2/síntesis química , Interleucina-2/genética , Interleucina-2/metabolismo , Interleucina-2/farmacología , Subunidad alfa del Receptor de Interleucina-2/química , Subunidad alfa del Receptor de Interleucina-2/metabolismo , Macrófagos/efectos de los fármacos , Fragmentos de Péptidos/síntesis química , Fragmentos de Péptidos/farmacología , Sustancias Protectoras/síntesis química , Sustancias Protectoras/farmacologíaRESUMEN
The review is focused on current issues of biomedical proteomics and peptidomics. The main attention is paid to modem proteomics technologies applied in medical research--extraction, detection and data analysis techniques. The use of chromatography, mass spectrometry and chromato mass spectrometry in proteogenomic, biomedical studies and biomarker discovery is discussed in detail.
Asunto(s)
Mezclas Complejas/química , Fragmentos de Péptidos/análisis , Proteínas/análisis , Proteómica , Animales , Biomarcadores/análisis , Investigación Biomédica , Cromatografía , Humanos , Espectrometría de Masas , Proteómica/métodosRESUMEN
In the current study the isolation and identification of Physcomitrella patens (Hedw.) B.S.G. moss peptides are described. Physcomitrella patens moss is actively used in recent years as a model organism to study the biology of plants. Protoplasts, protonemata and gametophores of the moss are demonstrated for the first time to contain diverse small peptides. From gametophores was isolated and identified 58 peptides that are fragments of 14 proteins, and from protonemata - 49 peptides, fragments of 15 proteins. It was found that the protonemata and gametophores Ph. patens, which are the successive stages of development of this plant, significantly different from each other as a peptide composition and the spectrum of the precursor protein of identified peptides. Isolation of protoplasts of the enzymatic destruction of cell wall protonemata accompanied by massive degradation of intracellular proteins, many of whom are proteins of photosynthesis, which is a characteristic response of plants to stress the impact of environmental factors. A total of moss protoplasts were isolated and identified 323 peptides that are fragments of 79 proteins.
Asunto(s)
Bryopsida/química , Péptidos/análisis , Proteínas de Plantas/análisis , Secuencia de Aminoácidos , Cromatografía en Gel , Biología Computacional , Datos de Secuencia Molecular , Proteínas de Plantas/aislamiento & purificación , Plastidios/química , Protoplastos/químicaRESUMEN
Review is devoted to studying the interaction muramyl peptides with protein components of immune system cells. Systems analysis of published results may be useful to select not only the strategy to further explore the function of this class of glycopeptides, but their use in clinical practice.
Asunto(s)
Acetilmuramil-Alanil-Isoglutamina/farmacología , Adyuvantes Inmunológicos/farmacología , Péptidos y Proteínas de Señalización Intracelular/metabolismo , Transducción de Señal/efectos de los fármacos , Inmunidad Adaptativa/efectos de los fármacos , Inmunidad Adaptativa/inmunología , Animales , Línea Celular , Humanos , Inmunidad Innata/efectos de los fármacos , Inmunidad Innata/inmunología , Proteínas Quinasas Activadas por Mitógenos/metabolismo , FN-kappa B/metabolismo , Proteína Adaptadora de Señalización NOD2/metabolismo , Mapeo de Interacción de Proteínas , Transducción de Señal/inmunología , Receptores Toll-Like/metabolismoRESUMEN
Profiles of endogenous peptides of the brain, heart, lungs, and spleen of a rat have been obtained by chromatographic and mass spectrometric analysis of low-molecular-mass fractions of tissues extracts. The concentrations of the corresponding components have been estimated from the intensities of 119 major chromatographic peaks. The total content of peptides in tissues, nmol/g (mg/g), was 3-13 (0.005-0.05) for the brain, 7-27 (0.01-0.10) for the heart, 17-68 (0.02-0.25) for the lungs, and 80-300 (0.08-1.30) for the spleen. A comparative analysis of the data obtained for the organs has been performed. The primary structures for 68 peptides have been determined; most substances (>70%) have been identified as hemoglobin fragments. It has been shown that many of the peptide components identified (>75%) are common for several organs. The relationship between the composition, the mechanism of formation, and the functional role of peptidomes of the organs, tissues, and cells of higher organisms has been discussed.
Asunto(s)
Química Encefálica , Pulmón/química , Miocardio/química , Péptidos/química , Péptidos/aislamiento & purificación , Bazo/química , Secuencia de Aminoácidos , Animales , Cromatografía Liquida , Femenino , Datos de Secuencia Molecular , Especificidad de Órganos , Ratas , Ratas Wistar , Espectrometría de Masa por Láser de Matriz Asistida de Ionización Desorción , Extractos de Tejidos/químicaRESUMEN
A new approach to the development of a vaccine against meningococci of serogroups A and B was proposed. It involves the synthesis of conjugates of high-molecular capsule polysaccharides of the serogroup A meningococcus (PsA) with earlier synthesized protective fragments of membrane proteins from serogroup B meningococci. The conjugates were synthesized using a method that consists of the generation of aldehyde groups by oxidizing free vicinal hydroxyl groups of PsA and subsequent reaction of these groups with amino groups of the peptide. The reaction proceeds with the intermediate formation of the Schiff base, which is reduced to the stable secondary amine. The main parameters of the reaction were optimized in the synthesis of a PsA conjugate with a model peptide and methods of their characterization were developed. The reproducibility and efficiency of the synthetic procedure were demonstrated by the example of synthesis of PsA conjugates with fragments of protein PorA from the outer membrane of the serogroup B meningococcus. It was shown that, when administered without adjuvant, a conjugate of PsA with a protective peptide, which represents an exposed conserved fragment 306-332 of protein PorA, stimulates the formation of antibodies to the peptide and polysaccharide moieties of the molecule and is also capable of decreasing the degree of bacteremia in animals infected with serogroup A and serogroup B meningococci. The approach can be applied to the development of a complex vaccine for serogroup A and serogroup B meningococci.
Asunto(s)
Antígenos Bacterianos/inmunología , Proteínas de la Membrana Bacteriana Externa/química , Vacunas Meningococicas/síntesis química , Neisseria meningitidis Serogrupo A/inmunología , Neisseria meningitidis Serogrupo B/inmunología , Fragmentos de Péptidos/química , Polisacáridos Bacterianos/química , Secuencia de Aminoácidos , Animales , Bacteriemia/inmunología , Bacteriemia/microbiología , Bacteriemia/prevención & control , Proteínas de la Membrana Bacteriana Externa/inmunología , Vacunas Meningococicas/inmunología , Ratones , Datos de Secuencia Molecular , Vacunas Sintéticas/química , Vacunas Sintéticas/inmunologíaRESUMEN
Using reverse-phase (MB-HIC 8 and HB-HIC 18) weak cation exchange (MB-WCX) and metal affinity ClinProt magnetoc beads peptides and protein factions were obtained from human sera for their profiling by MALDI-TOF mass spectrometry. Proteome profiling of sera from I-IV stage ovarian cancer patients (47 women, average age 51) and from healthy women (47 subjects, average age 49) using MB-WCX beads allowed calculation of the best diagnostic models based on the Genetic Algorithm and Supervised Neural Network classifiers; these model generated 100% sensitivity and specificity when the test set of subjects was analyzed. Introduction of additional sera from patients with colorectal cancer (19) and ulcerous colitis (5) to the statistical model confirmed 100% ovarian cancer recognition. Statistical mass-spectrometry analysis of mass-spectrometry peak areas included to the diagnostic classifiers showed 3 peaks distinctive for ovarian cancer and 4 peaks distinctive for ovarian and colorectal cancer.
Asunto(s)
Algoritmos , Biomarcadores de Tumor/sangre , Redes Neurales de la Computación , Neoplasias Ováricas/sangre , Neoplasias Ováricas/diagnóstico , Proteoma/análisis , Espectrometría de Masa por Láser de Matriz Asistida de Ionización Desorción , Proteínas Sanguíneas/análisis , Colitis Ulcerosa/sangre , Colitis Ulcerosa/diagnóstico , Neoplasias Colorrectales/sangre , Neoplasias Colorrectales/diagnóstico , Femenino , Humanos , Persona de Mediana Edad , Modelos Teóricos , Sensibilidad y EspecificidadRESUMEN
According to previously reported data, the supernatant of a primary culture of human erythrocytes contains 33 hemoglobin fragments. An analysis of the supernatant of a 20% (v/v) suspension of human erythrocytes allowed us to identify additionally four peptides whose precursors are cytoplasmic beta-actin (two fragments), fructose diphosphate aldolase B, and an unknown protein, as well as the amino acids tyrosine and tryptophan. The composition and the content of the components of the supernatant did not depend on the age or blood group of donors. The dynamics of accumulation in the supernatant (20-80 min of incubation) of the 14 hemoglobin fragments with the most reliably reproducible contents was obtained. The content of six peptides increased more than twofold between 20 and 40 min of incubation: the maximum increase in concentration was observed between 40 and 80 min (140%). The level of peptides that had the maximum concentration at the end of incubation was about 1000 pmol/ml of sedimented erythrocytes. The biological effects of the peptides identified in the supernatant of erythrocytes involve the stimulation of proliferation and hemopoiesis, suppression of proliferation, a bactericide effect, etc. These effects indicate the physiological importance of peptide release by erythrocytes. The English version of the paper: Russian Journal of Bioorganic Chemistry, 2008, vol. 34, no. 2; see also http://www.maik.ru.
Asunto(s)
Proteínas Sanguíneas/metabolismo , Eritrocitos/metabolismo , Péptidos/sangre , Adulto , Secuencia de Aminoácidos , Animales , Recuento de Células , Línea Celular Tumoral , Células Cultivadas , Cromatografía Líquida de Alta Presión , Eritrocitos/citología , Espacio Extracelular/metabolismo , Hemoglobinas/química , Hemoglobinas/metabolismo , Humanos , Masculino , Ratones , Persona de Mediana Edad , Datos de Secuencia Molecular , Fragmentos de Péptidos/sangre , Fragmentos de Péptidos/química , Fragmentos de Péptidos/farmacología , Péptidos/química , Péptidos/farmacologíaRESUMEN
The channel-forming activity of gramicidin A derivatives carrying positively charged amino acid sequences at their C-termini was studied on planar bilayer lipid membranes and liposomes. We showed previously that, at low concentrations, these peptides form classical cation-selective pores typical of gramicidin A, whereas, at high concentrations, they form large nonselective pores. The ability of the peptides to form nonselective pores, which was determined by the efflux of carboxyfluorescein, an organic dye, from liposomes, decreased substantially as the length of the gramicidin fragment in the series of cationic analogues was truncated. CD spectra showed that large pores are formed by peptides having both beta6.3 single-stranded and beta5.6 double-stranded helical conformations of the gramicidin fragment, with the C-terminal cationic sequence being extended. The dimerization of the peptides by the oxidation of the terminal cysteine promoted the formation of nonselective pores. It was shown that nonselective pores are not formed in membranes of erythrocytes, which may indicate a dependence of the channel-forming ability on the membrane type. The results may be of interest for the directed synthesis of peptides with antibacterial activity.
Asunto(s)
Antibacterianos/química , Gramicidina/análogos & derivados , Gramicidina/química , Canales Iónicos/química , Membrana Dobles de Lípidos/química , Secuencia de Aminoácidos , Dimerización , Membrana Eritrocítica/química , Gramicidina/síntesis química , Humanos , Liposomas/química , Péptidos/síntesis química , Péptidos/química , PorosidadRESUMEN
The level of proteolytic activity in tissues of oat seedlings was characterized under acidic conditions, and the number and content of the main components in low-molecular-mass fractions of the extract were determined. The structures of the majority of predominant peptide components isolated from the extract were studied. The use of a database of protein structures helped suggest possible structures of protein precursors of the peptides isolated. Detailed information on a plant peptidome was obtained for the first time.
Asunto(s)
Avena/química , Péptidos/aislamiento & purificación , Plantones/química , Cromatografía Líquida de Alta Presión , Péptidos/análisis , Proteínas de Plantas/químicaRESUMEN
Peptide fragments of conservative sites of PorA, OpaB, and NspA proteins of the outer membrane of serogroup B meningococci were synthesized. These peptides caused a pronounced protective effect in immunized mice infected with virulent homologous and heterologous strains of serogroups B and A meningococci. The protective effect appreciably increased, if the studied peptides were associated in a polycomponent preparation, which can be used in the construction of meningococcal bivalent B+A vaccine.
Asunto(s)
Proteínas de la Membrana Bacteriana Externa/inmunología , Neisseria meningitidis Serogrupo B/metabolismo , Péptidos/inmunología , Secuencia de Aminoácidos , Animales , Proteínas de la Membrana Bacteriana Externa/genética , Infecciones Meningocócicas/inmunología , Infecciones Meningocócicas/prevención & control , Vacunas Meningococicas , Ratones , Datos de Secuencia Molecular , Neisseria meningitidis Serogrupo B/química , Neisseria meningitidis Serogrupo B/patogenicidad , Péptidos/genéticaRESUMEN
Linear immunogenic peptides corresponding to amino acid sequences from the NS1 non-structural protein from tick-borne encephalitis virus (strain Sophyin) were predicted using established algorithms and synthesized. Of the 12 peptides predicted, 11 were able to induce peptide-specific antibodies in BALB/c mice but only 1 of these 11 was able to induce antibodies, which reacted with the native protein in a radio-immune precipitation assay. This peptide corresponds to amino acids 37--55, and forms one of the predicted structurally conserved alpha helices of the virus NS1 protein. It was able to protect 60% of animals against lethal challenge with the homologous highly pathogenic tick-borne encephalitis virus strain, and adoptive transfer experiments indicated the involvement of the antibodies induced by this peptide in its protective activity in mice.
Asunto(s)
Anticuerpos Antivirales/sangre , Virus de la Encefalitis Transmitidos por Garrapatas/inmunología , Encefalitis Transmitida por Garrapatas/prevención & control , Péptidos/síntesis química , Péptidos/inmunología , Proteínas no Estructurales Virales/inmunología , Secuencia de Aminoácidos , Animales , Anticuerpos Antivirales/inmunología , Especificidad de Anticuerpos , Modelos Animales de Enfermedad , Encefalitis Transmitida por Garrapatas/inmunología , Encefalitis Transmitida por Garrapatas/mortalidad , Inmunización , Ratones , Ratones Endogámicos BALB C , Datos de Secuencia Molecular , Péptidos/química , Proteínas no Estructurales Virales/química , Vacunas Virales/administración & dosificación , Vacunas Virales/inmunologíaRESUMEN
9- and 10-membered bridged dipeptides derived from L-aspartic acid and L- or D-glutamic acid were synthesized using aminoacyl incorporation reaction. Key intermediates containing internal pyroglutamyl moiety were prepared via side chain to backbone cyclization of related protected dipeptide derivatives of glutamic acid.
Asunto(s)
Ácido Aspártico/química , Dipéptidos/síntesis química , Ácido Glutámico/química , Lactamas/síntesis química , Hidrocarburos Aromáticos con Puentes/síntesis químicaRESUMEN
A number of protected proline-containing dipeptides Boc-Xaa-Pro-OBu(t) were converted via epimerization-free oxidation with RuO4 to dipeptides with an internal pyroglutamic acid residue, Boc-Xaa-Glp-OBu(t). The latter were subjected to oxidative Hoffman-type rearrangement induced by PhI[OC(O)CF3]2 to give N-(aminoacyl)-pyroglutamates. The behavior of these derivatives under basic conditions was studied, and for two such a derivatives an aminoacyl incorporation reaction was observed, producing otherwise poorly accessible 10-membered-ring dilactams derived from 1,4-diaminobutyric and glutamic acids in practicable yields.
Asunto(s)
Aminobutiratos/química , Ácido Glutámico/análogos & derivados , Ácido Glutámico/síntesis química , Péptidos Cíclicos/química , Péptidos Cíclicos/síntesis química , Aminoacilación , Ácido Glutámico/química , Estructura Molecular , Ornitina/química , Oxidación-Reducción , Ácido Pirrolidona Carboxílico/químicaRESUMEN
The antibodies to the bovine prion protein were produced by immunizing mice of three lines with five synthetic fragments of the protein and their six analogues. The analogues contained the amino acid substitutions that, according to theoretical calculation, should lead to an increase in the immunogenic activity of peptides. All the peptides, except for one, induced the formation of antibodies. All the sera containing the antipeptide antibodies were tested by an immunohistochemical method. The sera that were effectively bound to the brain preparations from the bovine with spongiform encephalopathy were identified; it was shown that they do not interact with the preparations of normal brain. Therefore, it was shown that the immunization of mice with the synthetic fragments of a prion protein helps obtain specific antibodies suitable for the study and diagnostics of prion diseases.
Asunto(s)
Anticuerpos Monoclonales/inmunología , Encéfalo/inmunología , Encefalopatía Espongiforme Bovina/inmunología , Fragmentos de Péptidos/inmunología , Priones/inmunología , Secuencia de Aminoácidos , Sustitución de Aminoácidos , Animales , Bovinos , Sueros Inmunes/inmunología , Inmunización , Técnicas para Inmunoenzimas , Ratones , Ratones Endogámicos BALB C , Ratones Endogámicos C57BL , Ratones Endogámicos CBA , Datos de Secuencia Molecular , Fragmentos de Péptidos/síntesis química , Especificidad de la EspecieRESUMEN
Previously unknown 9-membered bridged dipeptides derived from l or d isomers of 1,3-diaminopropionic acids and l-glutamic acid were synthesized using aminoacyl incorporation reaction. Key intermediates containing internal pyroglutamyl moiety were prepared via side chain to backbone cyclization of related protected dipeptide derivatives of glutamic acid.