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1.
Philos Trans A Math Phys Eng Sci ; 382(2273): 20230197, 2024 Jun 09.
Artículo en Inglés | MEDLINE | ID: mdl-38736334

RESUMEN

The origin of micrometeorites (MMs) from asteroids and comets is well-established, but the relative contribution from these two classes remains poorly resolved. Likewise, determining the precise origin of individual MMs is an open challenge. Here, cosmic-ray exposure ages are used to resolve the spatial origins of 12 MMs collected from urban areas and Antarctica. Their 26Al and 10Be concentration, produced during cosmic-ray irradiation in space, were measured by accelerator mass spectrometry. These data are compared to results from a model simulating the transport and irradiation of the MM precursors in space. This model, for the first time, considers a variety of orbits, precursor particle sizes, compositions and densities and incorporates non-isotropic solar and galactic cosmic-ray flux profiles, depth-dependent production rates, as well as spherical evaporation during atmospheric entry. While the origin for six MMs remains ambiguous, two MMs show a preferential tendency towards an origin in the Inner Solar System (Near Earth Objects to the Asteroid Belt) and four towards an origin in the Outer Solar System (Jupiter Family Comets to the Kuiper Belt). These findings challenge the notion that dust originating from the Outer Solar System is unlikely to survive long-term transport and delivery to the terrestrial planets. This article is part of the theme issue 'Dust in the Solar System and beyond'.

2.
J Chem Phys ; 154(2): 024501, 2021 Jan 14.
Artículo en Inglés | MEDLINE | ID: mdl-33445919

RESUMEN

Experimental studies of the glassy slowdown in molecular liquids indicate that the high-temperature activation energy E∞ of glass-forming liquids is directly related to their glass transition temperature Tg. To further investigate such a possible relation between high- and low-temperature dynamics in glass-forming liquids, we analyze the glassy dynamics of binary mixtures using molecular dynamics simulations. We consider a binary mixture of charged Lennard-Jones particles and vary the partial charges of the particles and, thus, the high-temperature activation energy and the glass transition temperature of the system. Based on previous results, we introduce a phenomenological model describing relaxation times over the whole temperature regime from high temperatures to temperatures well inside the supercooled regime. By investigating the dynamics of both particle species on molecular and diffusive length scales along isochoric and isobaric pathways, we find a quadratic charge dependence of both E∞ and Tg, resulting in an approximately constant ratio of both quantities independent of the underlying observable, the thermodynamic ensemble, and the particle species, and this result is robust against the actual definition of Tg. This generic relation between the activation energy and the glass transition temperature indicates that high-temperature dynamics and the glassy slowdown are related phenomena, and the knowledge of E∞ may allow us to approximately predict Tg.

3.
Sci Adv ; 7(14)2021 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-33789890

RESUMEN

Large airbursts, the most frequent hazardous impact events, are estimated to occur orders of magnitude more frequently than crater-forming impacts. However, finding traces of these events is impeded by the difficulty of identifying them in the recent geological record. Here, we describe condensation spherules found on top of Walnumfjellet in the Sør Rondane Mountains, Antarctica. Affinities with similar spherules found in EPICA Dome C and Dome Fuji ice cores suggest that these particles were produced during a single-asteroid impact ca. 430 thousand years (ka) ago. The lack of a confirmed crater on the Antarctic ice sheet and geochemical and 18O-poor oxygen isotope signatures allow us to hypothesize that the impact particles result from a touchdown event, in which a projectile vapor jet interacts with the Antarctic ice sheet. Numerical models support a touchdown scenario. This study has implications for the identification and inventory of large cosmic events on Earth.

4.
Trials ; 20(1): 523, 2019 Aug 22.
Artículo en Inglés | MEDLINE | ID: mdl-31439049

RESUMEN

BACKGROUND: The global prevalence of diabetes mellitus (DM) has been increasing over recent decades. In Germany, the prevalence for DM type 1 and type 2 in adults is estimated at about 7.7%. Hence, diabetes has to be classified as a serious public health concern. Being diagnosed with DM and facing possible sequelae might have a negative impact on patients' mental and physical well-being. However, diabetes not only affects patients themselves, but also their close relatives. To improve the quality of life for patients and relatives alike, the German Association of Diabetes Nurses and Education experts (VDBD) elaborated the first education program tailor-made for relatives of diabetes patients. This article describes the concept and design of the trial evaluating the efficacy of this education program called "DiaLife-Living Together with Diabetes". METHODS: This evaluation study is a cluster randomized controlled trial, in which the study centers will be randomly assigned either to the intervention group or the control group. Study centers will recruit relatives of and patients with DM type 1 and type 2. Members of the intervention group will participate in the education program DiaLife, whereas participants randomized in the control group will act as waiting-list controls. The study will assess the efficacy of DiaLife by comparing diabetes-related knowledge between the intervention and control groups as the primary outcome for participants. As the primary outcome in patients, the Hba1c value will be assessed. In addition, diabetes-related distress, family interaction, and other secondary endpoints will be considered as secondary outcomes. Long-term efficacy will be assessed 6 and 12 months after intervention. Hierarchical regression models will be used to analyze effects over time. DISCUSSION: While there is scientific evidence for the efficacy of education programs addressed to (diabetes) patients, there is a research gap with regard to intervention studies evaluating the efficacy of education programs designed for patients' relatives. The study results will provide information on the efficacy of the DiaLife education program. In addition, factors that might hinder a successful implementation of an education program for relatives will be identified. TRIAL REGISTRATION: German Clinical Trials Register, DRKS00015157 . Registered on 24 August 2018.


Asunto(s)
Diabetes Mellitus Tipo 1/terapia , Diabetes Mellitus Tipo 2/terapia , Familia/psicología , Educación en Salud/métodos , Conocimientos, Actitudes y Práctica en Salud , Adaptación Psicológica , Biomarcadores/sangre , Costo de Enfermedad , Diabetes Mellitus Tipo 1/sangre , Diabetes Mellitus Tipo 1/diagnóstico , Diabetes Mellitus Tipo 1/psicología , Diabetes Mellitus Tipo 2/sangre , Diabetes Mellitus Tipo 2/diagnóstico , Diabetes Mellitus Tipo 2/psicología , Relaciones Familiares , Alemania , Hemoglobina Glucada/metabolismo , Humanos , Estudios Multicéntricos como Asunto , Ensayos Clínicos Controlados Aleatorios como Asunto , Factores de Tiempo
5.
Urologe A ; 45(11): 1431-4, 2006 Nov.
Artículo en Alemán | MEDLINE | ID: mdl-16933122

RESUMEN

Adenomatoid tumor with intra-testicular localization is rare. Although most reported cases arise from the epididymis, rare cases have been reported in the testicular tunica, spermatic cord, ejaculatory ducts, prostate and suprarenal recess. Adenomatoid tumors occur in both sexes and are also found in the uterus, ovary and fallopian tubes of the female genital tract. Adenomatoid tumors are benign proliferations of mesothelial origin. We report the case of a 50-year-old male with an adenomatoid tumor of the left testis. Because of its rarity, the clinical, diagnostic and therapeutic aspects as well as the possibilities of testicular preservation are discussed.


Asunto(s)
Tumor Adenomatoide/diagnóstico , Neoplasias Testiculares/diagnóstico , Tumor Adenomatoide/patología , Biomarcadores de Tumor/análisis , Biopsia , Calbindina 2 , Diagnóstico Diferencial , Humanos , Queratinas/análisis , Masculino , Persona de Mediana Edad , Orquiectomía , Pronóstico , Proteína G de Unión al Calcio S100/análisis , Neoplasias Testiculares/patología , Testículo/patología , Tomografía Computarizada por Rayos X , Ultrasonografía , Vimentina/análisis
6.
Prog Biophys Mol Biol ; 73(1): 1-49, 2000.
Artículo en Inglés | MEDLINE | ID: mdl-10781828

RESUMEN

Raman optical activity (ROA) measures vibrational optical activity by means of a small difference in the intensity of Raman scattering from chiral molecules in right and left circularly polarized incident laser light. The ROA spectra of a wide range of biomolecules in aqueous solution can now be measured routinely. Because of its sensitivity to the chiral elements of biomolecular structure, ROA provides new information about solution structure and dynamics complementary to that supplied by conventional spectroscopic techniques. This article provides a brief introduction to the theory and practice of ROA spectroscopy followed by a review of recent ROA results on polypeptides, proteins, carbohydrates, nucleic acids and viruses which illustrate how new insight into current problems of structure, folding and function may be obtained from ROA studies.


Asunto(s)
Espectrometría Raman/métodos , Animales , Carbohidratos/química , Humanos , Ácidos Nucleicos/química , Péptidos/química , Proteínas/química , Virus/química
7.
J Mol Biol ; 261(3): 341-7, 1996 Aug 23.
Artículo en Inglés | MEDLINE | ID: mdl-8780777

RESUMEN

On account of its ability to discriminate between secondary, loop and sidegroup structure and its special sensitivity to conformational mobility, vibrational Raman optical activity (ROA) has provided new insights into the complexity of order within the molten globule state from measurements on alpha-lactalbumin at pH 2.0 over the temperature range 2 to 45 degrees C. Thus while much of the secondary structure present in the native protein persists with only a small gradual decrease with increasing temperature, the tertiary backbone fold changes dramatically, being almost complete and native-like at 2 degrees C and almost completely disordered at 35 degrees C. The change of the tertiary fold with temperature is cooperative but has no latent heat, and so has the approximate characteristics of a continuous phase transition, being of the order-disorder type since it involves the interconversion of rigid, locally-ordered loop structure with disordered mobile backbone structure. This has implications for protein folding because the long-range correlations that exist in the critical region of a continuous (but not in a first-order) phase transition could resolve, in principle, the problem of how the protein finds its native-like folding pattern at the molten globule stage.


Asunto(s)
Lactalbúmina/química , Pliegue de Proteína , Estructura Terciaria de Proteína , Espectrometría Raman
8.
J Mol Biol ; 254(4): 747-60, 1995 Dec 08.
Artículo en Inglés | MEDLINE | ID: mdl-7500347

RESUMEN

Proteins in aqueous solution are now accessible to Raman optical activity (ROA) measurements, which provide an incisive new probe of secondary and tertiary structure illustrated here by a study of bovine alpha-lactalbumin. The room-temperature ROA spectrum of native bovine alpha-lactalbumin is similar to that of native hen egg-white lysozyme except for features attributable to differences in the loop regions: in particular, a positive ROA band at approximately 1338 cm-1 assigned to conformationally homogeneous loop structure, possibly with local order corresponding to 3(10)-helix, has more than double the intensity in alpha-lactalbumin compared with lysozyme. This is consistent with the two proteins having similar secondary structure but different local details in the tertiary fold. ROA measurements on alpha-lactalbumin at pH 2.0 over a range of temperatures have provided a new perspective on the molten globule state. Thus at 35 degrees C ROA reveals the presence of some secondary structure but an almost complete loss of the tertiary loop structure; whereas at 2 degrees C the ROA spectrum is almost identical with that of the native protein, which is strong evidence that virtually all of the secondary structure and the tertiary backbone fold persist, albeit within a looser framework associated with increased solvent exposure and change of environment of many of the side-chains as evidenced by an increase in noise and bandwidth of some of the ROA signals together with aromatic fluorescence and near-UV circular dichroism signals characteristic of the molten globule state. Our sample of acid alpha-lactalbumin at 2 degrees C therefore appears to be an archetypal example of Ptitsyn's "native-like" molten globule, having a fixed native-like tertiary fold but with loss of tight packing of the side-chains; whereas at 35 degrees C it is a "disordered" molten globule. At 20 degrees C the acid molten globule appears to retain highly native-like secondary structure but with most of the tertiary fold already lost. A calcium-free sample of alpha-lactalbumin at neutral pH displayed a broad cooperative transition between native and molten globule states at approximately 15 degrees C, with the latter state showing similar but somewhat degraded tertiary loop ROA signatures to the native protein. In both the acid and apo molten globule states the ROA signatures of the secondary structure and the tertiary loops showed a gradual change with temperature.


Asunto(s)
Lactalbúmina/química , Muramidasa/química , Pliegue de Proteína , Estructura Terciaria de Proteína , Espectrometría Raman/métodos , Calcio/metabolismo , Lactalbúmina/metabolismo , Modelos Moleculares , Muramidasa/metabolismo , Conformación Proteica , Vibración
9.
J Mol Biol ; 290(1): 1-7, 1999 Jul 02.
Artículo en Inglés | MEDLINE | ID: mdl-10388553

RESUMEN

We report the first observations of vibrational Raman optical activity (ROA) on intact viruses. Specifically, ROA spectra of the filamentous bacteriophages Pf1, M13 and IKe in aqueous solution were measured in the range approximately 600-1800 cm-1. On account of its ability to probe directly the chiral elements of biomolecular structure, ROA has provided a new perspective on the solution structures of these well-studied systems. The ROA spectra of all three are dominated by signatures of helical elements in the major coat proteins, as expected from pre-existing data. The helical elements generate strong sharp positive ROA bands at approximately 1300 and 1342 cm-1in H2O solution, but in2H2O solution the approximately 1342 cm-1bands disappear completely. The spectra are similar to those of polypeptides under conditions that produce alpha-helical conformations. Our present results, together with results from other studies, suggest that the positive approximately 1342 cm-1ROA bands are generated by a highly hydrated form of alpha-helix, and that the positive approximately 1300 cm-1bands originate in alpha-helix in a more hydrophobic environment. The presence of significant amounts of highly hydrated helical sequences accords with the known flexibility of these viruses. Differences of spectral detail for Pf1, M13 and IKe demonstrate that ROA is sensitive to subtle variations of conformation and hydration within the major coat proteins, with M13 and IKe possibly containing more non-helical structure than Pf1. The ROA spectra of Pf1 at temperatures above and below that at which a structural transition is known to occur (approximately 10 degrees C) reveal little difference in the protein conformation between the two forms, but there are indications of changes in DNA structure.


Asunto(s)
Bacteriófagos/genética , ADN Viral/química , Conformación de Ácido Nucleico , Secuencia de Aminoácidos , Bacteriófagos/química , Cápside/química , Datos de Secuencia Molecular , Espectrometría Raman , Agua/química
10.
J Mol Biol ; 301(2): 553-63, 2000 Aug 11.
Artículo en Inglés | MEDLINE | ID: mdl-10926527

RESUMEN

The amyloidogenic prefibrillar partially denatured intermediate of human lysozyme, prepared by heating the native protein to 57 degrees C at pH 2.0, was studied using Raman optical activity (ROA). A positive band in the room temperature ROA spectrum of the native protein at approximately 1345 cm(-1), assigned to a hydrated form of alpha-helix, is not present in that of the prefibrillar intermediate, where a new strong positive band at approximately 1318 cm(-1) appears instead that is assigned to the poly(l-proline) II (PPII)-helical conformation. A sharp negative band at approximately 1241 cm(-1) in the native protein, assigned to beta-strand, shows little change in the ROA spectrum of the prefibrillar intermediate. The disappearance of a positive ROA band at approximately 1551 cm(-1) assigned to vibrations of tryptophan side-chains indicates that major conformational changes have occurred among the five tryptophan residues present in human lysozyme, four of which are located in the alpha-domain. The various ROA data suggest that a substantial loss of tertiary structure has occurred in the prefibrillar intermediate and that this is located more in the alpha-domain than in the beta-domain. There is no evidence for any increase in beta-structure. The ROA spectrum of hen lysozyme, which does not form amyloid fibrils so readily, remains much more native-like on heating to 57 degrees C at pH 2.0. The thermal behaviour of the alanine-rich alpha-helical peptide AK21 in aqueous solution was found to be similar to that of human lysozyme. Hydrated alpha-helix therefore appears to readily undergo a conformational change to PPII structure on heating, which may be a key step in the conversion of alpha-helix into beta-sheet in the formation of amyloid fibrils in human lysozyme. Since it is extended, flexible, lacks intrachain hydrogen bonds and is fully hydrated in aqueous solution, PPII helix has the appropriate characteristics to be implicated as a critical conformational element in many conformational diseases. Disorder of the PPII type may be a sine qua non for the formation of regular fibrils; whereas the more dynamic disorder of the random coil may lead only to amorphous aggregates.


Asunto(s)
Amiloide/química , Muramidasa/química , Péptidos/química , Animales , Pollos , Proteínas del Huevo/química , Calefacción , Humanos , Concentración de Iones de Hidrógeno , Proteínas de la Leche/química , Leche Humana/química , Desnaturalización Proteica , Estructura Terciaria de Proteína , Espectrometría Raman
11.
J Bone Miner Res ; 15(12): 2380-90, 2000 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-11127203

RESUMEN

Osteoblasts receive regulatory signals from hormones, growth factors, calcium, extracellular matrix, and other cells through a variety of receptors that utilize an array of signaling pathways and cytoplasmic messengers. This article addresses the nonuniform distribution of important signaling molecules (platelet-derived growth factor receptors [PDGFRs], nonreceptor tyrosine kinases, tyrosine kinase adaptor proteins, G proteins, and nitric oxide synthases [NOSs]) in the surface membranes of human and murine osteoblasts. We show that particular inner leaflet signaling molecules (e.g., heterotrimeric G proteins and Src family tyrosine kinases) are clustered and concentrated in Triton X-100-insoluble membranes that are enriched in caveolin, the major structural component of caveolae (50- to 100-nm flask-shaped invaginations of the plasma membrane that apparently are organized by oligomers of the protein caveolin). In addition, we show that a subset of highly ligand-responsive PDGFRs and mitogen-activated protein (MAP) kinase pathway effectors are present in the caveolin-enriched membrane fraction of osteoblasts.


Asunto(s)
Caveolas/metabolismo , Caveolinas/metabolismo , Proteínas de Unión al GTP/metabolismo , Óxido Nítrico Sintasa/metabolismo , Osteoblastos/metabolismo , Proteínas Tirosina Quinasas/metabolismo , Receptores del Factor de Crecimiento Derivado de Plaquetas/metabolismo , Animales , Caveolina 1 , Membrana Celular/metabolismo , Humanos , Immunoblotting , Ratones , Fosforilación , Pruebas de Precipitina , Ratas , Transducción de Señal , Tirosina/metabolismo
12.
Protein Sci ; 3(3): 435-9, 1994 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-7912598

RESUMEN

We have measured the aqueous solution vibrational Raman optical activity (ROA) spectra of concanavalin A, alpha-chymotrypsin, and beta-lactoglobulin, all of which are rich in beta-sheet, together with that of the model beta-turn peptide L-pro-L-leu-gly-NH2. Possible ROA signatures of antiparallel beta-sheet include a strong sharp positive band at approximately 1,313 cm-1 associated with backbone amide III C alpha H and NH deformations, and an amide I couplet, negative at low wavenumber and positive at high, centered at approximately 1,658 cm-1. Negative ROA bands in the range approximately 1,340-1,380 cm-1, which might originate in glycine CH2 deformations, appear to be characteristic of beta-turns. Our results provide further evidence that ROA is a more incisive probe of protein conformation than conventional vibrational spectroscopy, infrared, or Raman, because only those few vibrational coordinates within a given normal mode that sample the skeletal chirality directly contribute to the corresponding ROA band intensity.


Asunto(s)
Proteínas/química , Secuencia de Aminoácidos , Hormona Inhibidora de la Liberación de MSH/química , Modelos Químicos , Datos de Secuencia Molecular , Conformación Proteica , Estructura Secundaria de Proteína , Espectrometría Raman , Vibración
13.
Protein Sci ; 8(6): 1362-7, 1999 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-10386887

RESUMEN

We have studied the conformation of beta-lactoglobulin in aqueous solution at room temperature over the pH range approximately 2.0-9.0 using vibrational Raman optical activity (ROA). The ROA spectra clearly show that the basic up and down beta-barrel core is preserved over the entire pH range, in agreement with other studies. However, from the shift of a sharp positive ROA band at approximately 1268 to approximately 1294 cm(-1) on going from pH values below that of the Tanford transition, which is centered at pH approximately 7.5, to values above, the Tanford transition appears to be associated with changes in the local conformations of residues in loop sequences possibly corresponding to a migration into the alpha-helical region of the Ramachandran surface from a nearby region. These changes may be related to those detected in X-ray crystal structures which revealed that the Tanford transition is associated with conformational changes in loops which form a doorway to the interior of the protein. The results illustrate how the ability of ROA to detect loop and turn structure separately from secondary structure is useful for studying conformational plasticity in proteins.


Asunto(s)
Lactoglobulinas/química , Animales , Bovinos , Cristalografía por Rayos X , Concentración de Iones de Hidrógeno , Modelos Moleculares , Conformación Proteica , Espectrometría Raman
14.
Endocrinology ; 119(2): 470-80, 1986 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-3525118

RESUMEN

A protein kinase activity (S6PK) that phosphorylates ribosomal protein S6 has been detected in cytosolic extracts prepared from an insulin-sensitive mouse fibroblast-melanoma hybrid cell line. The activity of this enzyme is greatly increased in cells that have been stimulated with insulin or serum for 30 min before preparation of the extract. In the parental melanoma cells, which are insensitive to the growth-stimulatory action of insulin, the activity of the enzyme is lower than in the hybrid cells and is not increased in response to insulin. The insulin-sensitive, serum-sensitive S6PK from the hybrid cells is eluted as a single peak from diethylaminoethyl (DEAE)-cellulose between 0.15 and 0.2 M KCl. The apparent mol wt of the enzyme, as determined by gel permeation chromatography, is approximately 105,000. A second S6 kinase activity from the hybrid cells is trypsin dependent and elutes from DEAE-cellulose at a lower salt concentration than S6PK. In contrast to S6PK, the trypsin-dependent S6 kinase activity does not vary in a consistent manner in response to insulin or serum. Fractions obtained from DEAE-cellulose chromatography of extracts of the hybrid cells have also been assayed for ability to phosphorylate the synthetic octapeptide Arg-Arg-Leu-Ser-Ser-Leu-Arg-Ala (S6-1), the structure of which is based on a phosphorylated region of the S6 protein. Two trypsin-dependent peaks of protein kinase activity have been found to phosphorylate this peptide, one eluting at 0.05 M KCl and the other at 0.10-0.15 M KCl. The first peak elutes at the same salt concentration as the trypsin-dependent protein kinase(s) that phosphorylate ribosomal protein S6, while the second elutes slightly, but reproducibly ahead of S6PK. Several properties of the second peak of S6-1 phosphorylating activity suggest that it is not S6PK.


Asunto(s)
Fibroblastos/enzimología , Células Híbridas/enzimología , Insulina/farmacología , Melanoma/enzimología , Proteínas Quinasas/metabolismo , Proteínas Ribosómicas/metabolismo , Animales , Sangre , División Celular , Línea Celular , Cromatografía DEAE-Celulosa , Ratones , Oligopéptidos/metabolismo , Fosforilación , Proteína Quinasa C/metabolismo , Proteína S6 Ribosómica , Tripsina/farmacología
15.
Pediatrics ; 94(6 Pt 1): 878-82, 1994 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-7971005

RESUMEN

BACKGROUND AND OBJECTIVE: Although HIV counseling and testing of adolescents has increased rapidly in recent years due to increasing HIV seroprevalence rates, little is known about adolescents' use of HIV testing services. The aims of this study were to determine what proportion of high risk adolescent girls would use confidential HIV testing services linked to primary care and to explore the characteristics, beliefs, and experiences that distinguish those teenage girls who obtain HIV testing in this setting from those who do not. DESIGN: Prospective cohort study. SETTING: General pediatrics clinic with adolescent-specific appointments at a large urban HMO. PARTICIPANTS: Convenience sample of 124 adolescent girls engaging in risky behaviors identified by chart review before regularly scheduled clinic appointments. INTERVENTION: Subjects completed a self-report questionnaire assessing HIV-related knowledge, attitudes, beliefs, and behaviors before the medical visit. During their provider visit, teens were counseled about their risk behaviors and the availability of HIV testing services at the clinic. Subjects were also given the opportunity to view an educational video about HIV testing designed for adolescents. MAIN OUTCOME MEASURES: Use of HIV counseling and testing services at the clinic and HIV test results. RESULTS: Forty-one percent of these adolescent girls obtained HIV testing at the clinic on the day of their scheduled appointment. Univariate analysis revealed that adolescents who obtained testing had initiated sexual intercourse at a younger age (mean age 13.8 vs 14.4 years, P = .02) and were more likely to have had a prior discussion about HIV testing with a health care provider [RR = 2.02, 95% CIs (1.22, 3.36)]. Those who did not view the video were less likely to test [RR = 0.20, 95% CIs (0.07, 0.58)]. Multiple logistic regression modeling revealed that a prior discussion with a health care provider was the only independent predictor of obtaining an HIV test [OR = 3.47 95% CIs (1.26, 9.52)]. CONCLUSIONS: A significant proportion of adolescent girls engaging in risky behaviors will use confidential HIV counseling and testing services that are linked to primary care. Health care providers play an important role in helping teens address their risk for and concerns about HIV infection by engaging adolescents in repeated discussions about HIV testing.


Asunto(s)
Toma de Decisiones , Anticuerpos Anti-VIH/sangre , Personal de Salud , Psicología del Adolescente , Adolescente , Conducta del Adolescente/etnología , California , Estudios de Cohortes , Femenino , Conocimientos, Actitudes y Práctica en Salud , Humanos , Estudios Prospectivos , Asunción de Riesgos , Conducta Sexual/etnología , Conducta Sexual/estadística & datos numéricos , Encuestas y Cuestionarios , Población Urbana/estadística & datos numéricos
16.
Insect Biochem Mol Biol ; 30(8-9): 813-9, 2000.
Artículo en Inglés | MEDLINE | ID: mdl-10876125

RESUMEN

The vitellogenic cycle of the lubber grasshopper (Romalea microptera) was studied by measuring levels of juvenile hormone (JH III), vitellogenin, and vitellogenin-mRNA through the first oviposition cycle. JH III and vitellogenin were measured by radioimmunoassay (RIA) and enzyme-linked immunosorbent assay (ELISA), respectively. To measure vitellogenin-mRNA, a partial (753 bp) cDNA fragment of vitellogenin was isolated from the fat body of vitellogenic animals. The sequence of this cDNA was related to vitellogenin sequences in other insect species. Using these sequence data, an RT-PCR (reverse transcriptase polymerase chain reaction) assay was developed to quantify vitellogenin-mRNA levels during the oviposition cycle. Vitellogenin-mRNA levels in the fat body tissue from virgin females were measured on specific days after eclosion and compared to hemolymph levels of JH III and vitellogenin from the same individuals. The levels of all three compounds (JH III, vitellogenin, and vitellogenin-mRNA) showed similar changes throughout the oviposition cycle, being undetectable or nearly undetectable initially (day 3), rising to maximum levels on days 23 and 28, and then dropped to lower or undetectable levels on the day of oviposition. The ability to measure these characteristics will be useful for studying the effects of hormonal and nutritional manipulations on reproduction.


Asunto(s)
Genes de Insecto , Saltamontes/metabolismo , Oviposición/fisiología , ARN Mensajero , Sesquiterpenos/metabolismo , Vitelogeninas/genética , Vitelogeninas/metabolismo , Animales , Clonación Molecular , ADN Complementario , Femenino , Saltamontes/genética , Saltamontes/fisiología , Masculino , Ovario/fisiología , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa/métodos
17.
Sci Prog ; 81 ( Pt 1): 17-34, 1998.
Artículo en Inglés | MEDLINE | ID: mdl-9567775

RESUMEN

Determination of the solution structure and function of biomolecules such as proteins, carbohydrates and nucleic acids remains at the forefront of biomedical research. Thanks to recent developments in instrumentation, biomolecules can now be studied using Raman optical activity (ROA), a novel technique which measures vibrational optical activity in chiral molecules by means of a small difference in the intensity of Raman scattering in right- and left-circularly polarized incident laser light. This article reviews recent progress in the application of ROA to the determination of the solution structure and dynamics of proteins, carbohydrates and nucleic acids.


Asunto(s)
Conformación de Carbohidratos , Conformación de Ácido Nucleico , Conformación Proteica , Espectrometría Raman , Modelos Moleculares
18.
Talanta ; 40(4): 545-9, 1993 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-18965664

RESUMEN

Experimental and theoretical vibrational Raman optical activity (VROA) spectra of (2R,3R)-2,3-dimethylthiirane in the 200-1500 cm(-1) region are presented. The level of agreement obtained for the observed and predicted VROA signs suggests that the absolute configurations of chiral molecules can be determined confidently using VROA.

19.
Int J Biol Macromol ; 16(5): 277-8, 1994 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-7893631

RESUMEN

This paper reports the first vibrational Raman optical activity (ROA) spectrum of a glycoprotein. The sample, orosomucoid (alpha 1-acid glycoprotein), shows ROA bands characteristic of a high beta-sheet content together with new bands which could be specific for the carbohydrate and its association with the protein. Our results suggest that ROA spectra of intact glycoproteins may contain information about both protein and carbohydrate conformation and the mutual influence on each other's stability and conformation.


Asunto(s)
Glicoproteínas/química , Espectrometría Raman , Conformación de Carbohidratos , Humanos , Orosomucoide/química , Conformación Proteica , Vibración
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