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2.
Ecol Appl ; 20(8): 2131-47, 2010 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-21265447

RESUMO

The distributions of animal populations change and evolve through time. Migratory species exploit different habitats at different times of the year. Biotic and abiotic features that determine where a species lives vary due to natural and anthropogenic factors. This spatiotemporal variation needs to be accounted for in any modeling of species' distributions. In this paper we introduce a semiparametric model that provides a flexible framework for analyzing dynamic patterns of species occurrence and abundance from broad-scale survey data. The spatiotemporal exploratory model (STEM) adds essential spatiotemporal structure to existing techniques for developing species distribution models through a simple parametric structure without requiring a detailed understanding of the underlying dynamic processes. STEMs use a multi-scale strategy to differentiate between local and global-scale spatiotemporal structure. A user-specified species distribution model accounts for spatial and temporal patterning at the local level. These local patterns are then allowed to "scale up" via ensemble averaging to larger scales. This makes STEMs especially well suited for exploring distributional dynamics arising from a variety of processes. Using data from eBird, an online citizen science bird-monitoring project, we demonstrate that monthly changes in distribution of a migratory species, the Tree Swallow (Tachycineta bicolor), can be more accurately described with a STEM than a conventional bagged decision tree model in which spatiotemporal structure has not been imposed. We also demonstrate that there is no loss of model predictive power when a STEM is used to describe a spatiotemporal distribution with very little spatiotemporal variation; the distribution of a nonmigratory species, the Northern Cardinal (Cardinalis cardinalis).


Assuntos
Ecossistema , Monitoramento Ambiental/métodos , Modelos Biológicos , Animais , Aves Canoras/fisiologia , Especificidade da Espécie , Fatores de Tempo , Estados Unidos
3.
Oral Microbiol Immunol ; 21(1): 61-8, 2006 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-16390343

RESUMO

INTRODUCTION: Molecular ecological analysis based on 16S rRNA gene sequence analysis is well established for the characterisation of complex bacterial communities. However, 'universal' PCR primers can introduce biases into the analysis of the species composition of clone libraries because of mismatches between the primer and target organism sequences. In this study, three universal primer sets were compared for the analysis of the microflora in subgingival plaque. METHODS: Three subgingival plaque samples were collected from two subjects with localised severe chronic periodontitis. Half of each sample was cultured while DNA was extracted from the remaining half and 16S rDNA amplified with universal primer pairs 27F, 1525R (A); 27F, 1492R (B) and 530F, 1525R (C). Amplified genes were cloned, sequenced and identified by comparison with 16S rRNA databases. RESULTS: 137 taxa were identified among 177 isolates and 417 clones sequenced. Of these, 86 were detected only by the molecular technique whereas 26 were found only by culture. Sequences from 81 taxa did not correspond to those of named species and of these, 38 were not represented in the nucleotide databases. 16S RNA genes for these 38 taxa were sequenced and deposited with GenBank. CONCLUSION: The use of three sets of universal primers allowed the identification of 38 novel bacterial phylotypes. There were marked differences in the composition of the libraries generated by the different primer sets. A combination of molecular and cultural techniques is recommended to maximise the coverage of detection of bacterial taxa in oral samples.


Assuntos
Bactérias/classificação , Placa Dentária/microbiologia , Gengiva/microbiologia , Reação em Cadeia da Polimerase/métodos , Bactérias/genética , Técnicas Bacteriológicas , Bacteroidetes/classificação , Sequência de Bases , Doença Crônica , Clonagem Molecular , DNA Bacteriano/genética , DNA Ribossômico/genética , Amplificação de Genes , Biblioteca Gênica , Bactérias Gram-Positivas/classificação , Humanos , Periodontite/microbiologia , Filogenia , RNA Ribossômico 16S/genética , Selenomonas/classificação , Spirochaetales/classificação , Streptococcus/classificação
4.
J Clin Microbiol ; 42(7): 3023-9, 2004 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-15243054

RESUMO

Molecular techniques have revealed many novel, presumed unculturable, taxa in oral infections. The aim of this study was to characterize the bacterial community of the middle and advancing front of carious dental lesions by cultural and molecular analyses. Samples were collected with a hand excavator from five teeth with carious lesions involving dentine. Samples were cultured on blood agar and Rogosa agar incubated in air plus 5% CO(2) and on fastidious anaerobe agar anaerobically. DNA was also extracted directly from the samples and 16S rRNA genes were amplified by PCR with universal primers. PCR products were singularized by cloning, and the cloned inserts and cultured isolates were identified by 16S rRNA gene sequence analysis. We identified 95 taxa among the 496 isolates and 1,577 clones sequenced; 44 taxa were detected by the molecular method alone; 31 taxa were previously undescribed. Only three taxa, Streptococcus mutans, Rothia dentocariosa, and an unnamed Propionibacterium sp., were found in all five samples. The predominant taxa by anaerobic cultivation were the novel Propionibacterium sp. (18%), Olsenella profusa (14%), and Lactobacillus rhamnosus (8%). The predominant taxa in the molecular analysis were Streptococcus mutans (16%), Lactobacillus gasseri/johnsonii (13%), and Lactobacillus rhamnosus (8%). There was no significant difference between the compositions of the microflora in the middle and advancing front samples (P < 0.05, Wilcoxon matched pairs, signed ranks test). In conclusion, combined cultural and molecular analyses have shown that a diverse bacterial community is found in dentinal caries and that numerous novel taxa are present.


Assuntos
Bactérias/isolamento & purificação , Cárie Dentária/microbiologia , Adulto , Idoso , Bactérias/genética , Genes de RNAr , Humanos , Masculino , Pessoa de Meia-Idade , Filogenia , RNA Ribossômico 16S/genética , Análise de Sequência de DNA
5.
Neuroscience ; 123(3): 675-85, 2004.
Artigo em Inglês | MEDLINE | ID: mdl-14706779

RESUMO

Prepulse inhibition (PPI) of startle is a measure of sensorimotor gating that is impaired in schizophrenia. We have reported that PPI is regulated by the ventral hippocampus (VH) and that the PPI disruptive effects of the dopamine agonist apomorphine are enhanced 4 weeks after excitotoxic lesions of the VH. The mechanisms responsible for the VH influence on PPI are not understood, but have been ascribed to interactions between the VH and nucleus accumbens. In the present study, we examined whether the VH influence on PPI and its dopaminergic regulation is dependent on the integrity of the VH-accumbens projection via the fornix. First, the PPI-disruptive effects of intra-VH NMDA infusion were assessed after sham or electrolytic transection of the fornix. Second, the PPI-disruptive effects of apomorphine were assessed 1 month after excitotoxic or electrolytic lesions of the VH, or after fornix transection. Intra-VH N-methyl-D-aspartate infusion significantly disrupted PPI; this effect was unaffected by fornix lesions. The PPI-disruptive effects of apomorphine were significantly enhanced by excitotoxic or electrolytic lesions of the VH, but not by fornix transection. The influence of the VH on PPI and its dopaminergic regulation does not appear to be mediated via the fornix. The enhanced sensitivity to the PPI-disruptive effects of apomorphine after VH lesions is not dependent on excitotoxin-induced changes in the VH or its downstream projections.


Assuntos
Apomorfina/farmacologia , Fórnice/efeitos dos fármacos , Hipocampo/efeitos dos fármacos , Inibição Neural/efeitos dos fármacos , Reflexo de Sobressalto/efeitos dos fármacos , Animais , Fórnice/fisiologia , Hipocampo/fisiologia , Inibição Neural/fisiologia , Ratos , Ratos Sprague-Dawley , Reflexo de Sobressalto/fisiologia
6.
Phytomedicine ; 11(7-8): 567-75, 2004 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-15636169

RESUMO

Alternative and complementary therapeutic approaches, such as the use of a wide array of herbal, nutritional, and physical manipulations, are becoming popular for relieving symptoms of osteoarthritis (OA). The present study evaluated the efficacy of soy protein (SP) supplementation in relieving the pain and discomfort associated with OA. One hundred and thirty-five free-living individuals (64 men and 71 women) with diagnosed OA or with self-reported chronic knee joint pain not attributed to injury or rheumatoid arthritis were recruited for this double-blind, placebo-controlled, parallel design study. Study participants were assigned randomly to consume 40 g of either supplemental SP or milk-based protein (MP) daily for 3 months. Pain, knee range of motion, and overall physical activity were evaluated prior to the start of treatment and monthly thereafter. Serum levels of glycoprotein 39 (YKL-40), a marker of cartilage degradation, and insulin-like growth factor-I (IGF-I), a growth factor associated with cartilage synthesis, were assessed at baseline and at the end of the study. Overall, SP improved OA-associated symptoms such as range of motion and several factors associated with pain and quality of life in comparison to MP. However, these beneficial effects were mainly due to the effect of SP in men rather than women. Biochemical markers of cartilage metabolism further support the efficacy of SP in men as indicated by a significant increase in serum level of IGF-I and a significant decrease in serum level of YKL-40 compared to MP. This study is the first to provide evidence of possible beneficial effects of SP in the management of OA. Examining and verifying the long-term effects of SP on improving symptoms of OA, particularly in men, is warranted.


Assuntos
Osteoartrite/tratamento farmacológico , Proteínas de Soja/uso terapêutico , Adulto , Idoso , Método Duplo-Cego , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Osteoartrite/complicações , Dor/tratamento farmacológico , Dor/etiologia , Qualidade de Vida
7.
Int J Syst Evol Microbiol ; 53(Pt 6): 1937-40, 2003 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-14657126

RESUMO

Six strains of anaerobic, Gram-negative coccobacilli isolated from the root canals of patients with endodontic infections (five strains) and from a deep periodontal pocket (one strain) were subjected to a comprehensive range of phenotypic and genetic tests and were found to comprise a homogeneous group. Following 16S rRNA gene sequence analysis, they were found to be most closely related to Dialister pneumosintes, with 93 % sequence similarity between the two taxa. A novel species, Dialister invisus sp. nov., is proposed. Biochemically, the species is largely unreactive and is asaccharolytic, with only traces of acetate and propionate detected as metabolic end-products. The G+C content of the DNA of D. invisus strains is 45-46 mol%. The type strain is E7.25(T) (=CCUG 47026(T)=DSM 15470(T)).


Assuntos
Bactérias Gram-Positivas Formadoras de Endosporo/classificação , Mucosa Bucal/microbiologia , Filogenia , Proteínas de Bactérias/genética , Bactérias Gram-Positivas Formadoras de Endosporo/genética , Bactérias Gram-Positivas Formadoras de Endosporo/isolamento & purificação , Humanos , Microscopia Eletrônica , Dados de Sequência Molecular
8.
FEMS Microbiol Ecol ; 44(3): 361-71, 2003 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-19719617

RESUMO

Abstract Sulphate-reducing bacteria (SRB) and methanogenic archaea (MA) are important anaerobic terminal oxidisers of organic matter. However, we have little knowledge about the distribution and types of SRB and MA in the environment or the functional role they play in situ. Here we have utilised sediment slurry microcosms amended with ecologically significant substrates, including acetate and hydrogen, and specific functional inhibitors, to identify the important SRB and MA groups in two contrasting sites on a UK estuary. Substrate and inhibitor additions had significant effects on methane production and on acetate and sulphate consumption in the slurries. By using specific 16S-targeted oligonucleotide probes we were able to link specific SRB and MA groups to the use of the added substrates. Acetate consumption in the freshwater-dominated sediments was mediated by Methanosarcinales under low-sulphate conditions and Desulfobacter under the high-sulphate conditions that simulated a tidal incursion. In the marine-dominated sediments, acetate consumption was linked to Desulfobacter. Addition of trimethylamine, a non-competitive substrate for methanogenesis, led to a large increase in Methanosarcinales signal in marine slurries. Desulfobulbus was linked to non-sulphate-dependent H(2) consumption in the freshwater sediments. The addition of sulphate to freshwater sediments inhibited methane production and reduced signal from probes targeted to Methanosarcinales and Methanomicrobiales, while the addition of molybdate to marine sediments inhibited Desulfobulbus and Desulfobacterium. These data complement our understanding of the ecophysiology of the organisms detected and make a firm connection between the capabilities of species, as observed in the laboratory, to their roles in the environment.

9.
J Dent Res ; 81(11): 761-6, 2002 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-12407091

RESUMO

Cultural studies have indicated that a subset of the oral microflora is responsible for endodontic infections. Approximately 50% of oral bacteria are unculturable, so it is likely that currently unknown bacteria are present in such infections. In this study, cultural and molecular analyses were performed on the microflora in aspirate samples collected from 5 infected root canals. 16S rDNA sequences from 261 isolates and 624 clones were identified by comparison with database sequences. Sixty-five taxa were identified, of which 26 were found by the molecular method alone. A mean of 20.2 taxa was found in each sample. A new species of Dialister was the only organism present in all 5 samples. Twenty-seven novel taxa were detected, 18 of which belonged to the phylum Firmicutes and 8 to Bacteroidetes. Culture-independent, molecular analysis has revealed a more diverse microflora associated with endodontic infections than that revealed by cultural methods alone.


Assuntos
Bactérias Anaeróbias/isolamento & purificação , Bactérias Anaeróbias/patogenicidade , Infecções Bacterianas/microbiologia , DNA Bacteriano/análise , Periodontite Periapical/microbiologia , Adulto , Técnicas de Tipagem Bacteriana , Contagem de Colônia Microbiana , DNA Ribossômico/análise , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , RNA Ribossômico 16S/análise
10.
J Dent ; 30(7-8): 359-63, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12554119

RESUMO

OBJECTIVES: Previous studies have evaluated bacterial numbers in carious dentine using conventional culturing methods, capable of detecting only a proportion of the total bacteria present within lesions. The aim of this study was to detect and enumerate the total bacterial population present in carious human dentine by means of fluorescent in situ hybridisation. METHOD: Five freshly extracted carious molars were sequentially hand excavated under sterile conditions through four levels in the lesions. Replicate samples were probed with a rhodamine-tagged, 16S rRNA-directed probe (EUB338), specific for the bacterial domain. Two of the five original samples were examined using fluorescence microscopy and by using a systematic visual counting strategy; direct enumeration of the bacterial population in carious dentine was performed. RESULTS: In the superficial, middle and deep/excavation front zones, a mean of 7.34 x 10(6) (standard error of the mean, SEM +/- 0.44), 5.23 x 10(6) (SEM +/- 0.18), and 1.69 x 10(6) (SEM +/- 0.15) total bacteria/mg dentine were found, respectively. In the advancing front zone (beyond the conventional clinical excavation boundary) a mean of 0.34 x 10(6) (SEM +/- 0.05) total bacteria/mg dentine was recorded. CONCLUSION: A bacterial enumeration strategy was developed and detected greater numbers of bacteria through the depth of carious lesions that had been reported previously. The technique could be further developed using species-specific probes to determine the distribution, abundance and viability of all bacteria in carious dentine. This new information in turn will lead to a better understanding of the pathological process of caries and ultimately, its clinical treatment.


Assuntos
Cárie Dentária/microbiologia , Dentina/microbiologia , Hibridização in Situ Fluorescente/métodos , Bactérias/isolamento & purificação , Proteínas de Bactérias/análise , Humanos , Dente Molar/microbiologia
11.
Fund Raising Manage ; 32(2): 28-30, 2001 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-11409083

RESUMO

Organizations that sell sponsorship "properties" need to understand that when corporate donors give generously to causes, they do so with specific marketing objectives in mind.


Assuntos
Comércio/organização & administração , Obtenção de Fundos/organização & administração , Objetivos Organizacionais , Internet , Salários e Benefícios , Estados Unidos
12.
Nat Biotechnol ; 19(5): 461-5, 2001 May.
Artigo em Inglês | MEDLINE | ID: mdl-11329017

RESUMO

We have developed a rapid diffusion immunoassay that allows measurement of small molecules down to subnanomolar concentrations in <1 min. This competitive assay is based on measuring the distribution of a labeled probe molecule after it diffuses for a short time from one region into another region containing antigen-specific antibodies. The assay was demonstrated in the T-sensor, a simple microfluidic device that places two fluid streams in contact and allows interdiffusion of their components. The model analyte was phenytoin, a typical small drug molecule. Clinically relevant levels were measured in blood diluted from 10- to 400-fold in buffer containing the labeled antigen. Removal of cells from blood samples was not necessary. This assay compared favorably with fluorescence polarization immunoassay (FPIA) measurements. Numerical simulations agree well with experimental results and provide insight for predicting assay performance and limitations. The assay is homogeneous, requires <1 microl of reagents and sample, and is applicable to a wide range of analytes.


Assuntos
Imunoensaio/métodos , Reologia/instrumentação , Especificidade de Anticorpos , Complexo Antígeno-Anticorpo/análise , Complexo Antígeno-Anticorpo/sangue , Ligação Competitiva , Difusão , Imunoensaio de Fluorescência por Polarização , Peso Molecular , Fenitoína/análise , Fenitoína/sangue , Reologia/economia , Reologia/métodos
13.
J Lesbian Stud ; 5(3): 129-35, 2001.
Artigo em Inglês | MEDLINE | ID: mdl-24802832

RESUMO

ABSTRACT Marcia Munson, a feminist, gay rights, and environmental activist for the last thirty years, has chosen to reserve a significant portion of her life for doing volunteer work by living simply and working part time at the IRS (Internal Revenue Service). While choosing to retain the simple lifestyle of the "70s in order to pursue her activist dreams, the author recognizes that the "70s model of self-funded activism no longer works today. During the 1970s, volunteers were often able to support their projects with funds from their own pockets, or could scrape by on small salaries provided by CETA grants and work-study money. In the 1980s, fundraising events to raise money gained popularity. By the 1990s, many non-profit organizations operated primarily with paid staff, and the main volunteer activity had become raising money. Looking back at "70s activism, Munson points out that the services of a skilled, experienced volunteer can be as valuable as money to an organization.

14.
Nat Struct Biol ; 7(10): 894-902, 2000 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11017200

RESUMO

In the eukaryotic secretory and endocytic pathways, transport vesicles shuttle cargo among intracellular organelles and to and from the plasma membrane. Cargo delivery entails fusion of the transport vesicle with its target, a process thought to be mediated by membrane bridging SNARE protein complexes. Temporal and spatial control of intracellular trafficking depends in part on regulating the assembly of these complexes. In vitro, SNARE assembly is inhibited by the closed conformation adopted by the syntaxin family of SNAREs. To visualize this closed conformation directly, the X-ray crystal structure of a yeast syntaxin, Sso1p, has been determined and refined to 2.1 A resolution. Mutants designed to destabilize the closed conformation exhibit accelerated rates of SNARE assembly. Our results provide insight into the mechanism of SNARE assembly and its intramolecular and intermolecular regulation.


Assuntos
Proteínas Fúngicas/metabolismo , Proteínas de Membrana/metabolismo , Proteínas de Saccharomyces cerevisiae , Saccharomyces cerevisiae/metabolismo , Proteínas de Transporte Vesicular , Sequência de Aminoácidos , Cristalografia por Raios X , Análise Mutacional de DNA , Proteínas Fúngicas/química , Proteínas Fúngicas/genética , Proteínas de Membrana/química , Proteínas de Membrana/genética , Modelos Moleculares , Dados de Sequência Molecular , Neurônios/metabolismo , Conformação Proteica , Proteínas Qa-SNARE , Proteínas SNARE , Homologia de Sequência de Aminoácidos
15.
Int J Syst Bacteriol ; 49 Pt 4: 1939-41, 1999 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-10555379

RESUMO

The recently proposed species Eubacterium minutum and Eubacterium tardum appeared to be similar from their published descriptions. The aim of this study was to perform phenotypic and genetic analyses of strains of both species to clarify their taxonomic position. The type strains of E. minutum and E. tardum exhibited identical biochemical and protein profiles and their 16S rRNA gene sequences displayed 99.9% similarity. The G + C content of the DNA of both strains was estimated at 45 mol%. It is concluded that E. minutum and E. tardum are synonyms; E. minutum has priority. An emended description of E. minutum is given.


Assuntos
Eubacterium/classificação , Eubacterium/genética , Técnicas de Tipagem Bacteriana , Composição de Bases , DNA Bacteriano/química , DNA Bacteriano/genética , Eletroforese em Gel de Poliacrilamida , Eubacterium/química , Genes de RNAr , Dados de Sequência Molecular , Reação em Cadeia da Polimerase , RNA Ribossômico 16S/genética , Análise de Sequência de DNA , Terminologia como Assunto
16.
J Cell Biol ; 146(2): 333-44, 1999 Jul 26.
Artigo em Inglês | MEDLINE | ID: mdl-10427089

RESUMO

Proteins of the Sec1 family have been shown to interact with target-membrane t-SNAREs that are homologous to the neuronal protein syntaxin. We demonstrate that yeast Sec1p coprecipitates not only the syntaxin homologue Ssop, but also the other two exocytic SNAREs (Sec9p and Sncp) in amounts and in proportions characteristic of SNARE complexes in yeast lysates. The interaction between Sec1p and Ssop is limited by the abundance of SNARE complexes present in sec mutants that are defective in either SNARE complex assembly or disassembly. Furthermore, the localization of green fluorescent protein (GFP)-tagged Sec1p coincides with sites of vesicle docking and fusion where SNARE complexes are believed to assemble and function. The proposal that SNARE complexes act as receptors for Sec1p is supported by the mislocalization of GFP-Sec1p in a mutant defective for SNARE complex assembly and by the robust localization of GFP-Sec1p in a mutant that fails to disassemble SNARE complexes. The results presented here place yeast Sec1p at the core of the exocytic fusion machinery, bound to SNARE complexes and localized to sites of secretion.


Assuntos
Adenosina Trifosfatases , Exocitose , Fusão de Membrana , Proteínas de Membrana/metabolismo , Proteínas do Tecido Nervoso/metabolismo , Proteínas de Saccharomyces cerevisiae , Proteínas de Transporte Vesicular , Proteínas rab de Ligação ao GTP , Trifosfato de Adenosina/metabolismo , Proteínas Fúngicas/genética , Proteínas Fúngicas/metabolismo , Proteínas de Ligação ao GTP/genética , Proteínas de Ligação ao GTP/metabolismo , Proteínas de Membrana/genética , Proteínas Munc18 , Proteínas do Tecido Nervoso/genética , Testes de Precipitina , Ligação Proteica , Proteínas Qa-SNARE , Proteínas Qc-SNARE , Proteínas Recombinantes de Fusão/genética , Proteínas Recombinantes de Fusão/metabolismo , Proteínas SNARE , Saccharomyces cerevisiae/citologia , Saccharomyces cerevisiae/genética , Saccharomyces cerevisiae/metabolismo , Temperatura
17.
Adv Data ; (309): 1-11, 1999 Dec 22.
Artigo em Inglês | MEDLINE | ID: mdl-11067566

RESUMO

OBJECTIVE: This report presents demographic characteristics, service utilization, and primary admission diagnoses of elderly users of home health care services. Included are home health care services used by both current and discharged clients (called patients). These services are provided by home health care agencies and hospices. The focus of the report is on services used by both current patients and discharges aged 65 years and over. METHODS: The data used for this report are from the National Center for Health Statistics 1996 National Home and Hospice Care Survey's (NHHCS) sample of current patients and discharges. The 1996 NHHCS is the fourth survey of home health care agencies and hospices and their current patients and discharges. RESULTS: The overall results of the survey indicate that, as in previous years, the elderly current patients and discharges were predominantly women, 75-84 years old, white, non-Hispanic, widowed, and most often lived in a private residence with members of their family. For elderly men and women, the most commonly used home health care service was skilled nursing services and the primary admission diagnosis was diseases of the circulatory system, including heart disease.


Assuntos
Inquéritos Epidemiológicos , Serviços de Assistência Domiciliar/estatística & dados numéricos , Hospitais para Doentes Terminais/estatística & dados numéricos , Atividades Cotidianas , Idoso , Idoso de 80 Anos ou mais , Demografia , Feminino , Humanos , Masculino , Admissão do Paciente/estatística & dados numéricos , Alta do Paciente/estatística & dados numéricos , Estados Unidos
18.
J Lesbian Stud ; 3(1-2): 1-7, 1999.
Artigo em Inglês | MEDLINE | ID: mdl-24786019
19.
J Lesbian Stud ; 3(1-2): 209-16, 1999.
Artigo em Inglês | MEDLINE | ID: mdl-24786042

RESUMO

SUMMARY In recent years, concern about transmission of AIDS and other STDs has prompted people of all sexual orientations to use various safer sex techniques. This article explains why monogamy is not necessarily any safer than polyamory. Research on the low risk of woman-to-woman transmission of HIV and other STDs is described.

20.
Nat Struct Biol ; 5(9): 793-802, 1998 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-9731774

RESUMO

The fusion of intracellular transport vesicles with their target membranes requires the assembly of SNARE proteins anchored in the apposed membranes. Here we use recombinant cytoplasmic domains of the yeast SNAREs involved in Golgi to plasma membrane trafficking to examine this assembly process in vitro. Binary complexes form between the target membrane SNAREs Sso1p and Sec9p; these binary complexes can subsequently bind to the vesicle SNARE Snc2p to form ternary complexes. Binary and ternary complex assembly are accompanied by large increases in alpha-helical structure, indicating that folding and complex formation are linked. Surprisingly, we find that binary complex formation is extremely slow, with a second-order rate constant of approximately 3 M(-1) s(-1). An N-terminal regulatory domain of Sso1p accounts for slow assembly, since in its absence complexes assemble 2,000-fold more rapidly. Once binary complexes form, ternary complex formation is rapid and is not affected by the presence of the regulatory domain. Our results imply that proteins that accelerate SNARE assembly in vivo act by relieving inhibition by this regulatory domain.


Assuntos
Proteínas Fúngicas/química , Proteínas Fúngicas/metabolismo , Proteínas de Membrana/química , Proteínas de Membrana/metabolismo , Proteínas de Saccharomyces cerevisiae , Proteínas de Transporte Vesicular , Dicroísmo Circular , Estabilidade de Medicamentos , Proteínas Fúngicas/genética , Cinética , Substâncias Macromoleculares , Fusão de Membrana/fisiologia , Proteínas de Membrana/genética , Modelos Biológicos , Fragmentos de Peptídeos/química , Fragmentos de Peptídeos/genética , Fragmentos de Peptídeos/metabolismo , Conformação Proteica , Dobramento de Proteína , Proteínas Qa-SNARE , Proteínas Recombinantes de Fusão/química , Proteínas Recombinantes de Fusão/genética , Proteínas Recombinantes de Fusão/metabolismo , Proteínas SNARE , Saccharomyces cerevisiae/genética , Saccharomyces cerevisiae/metabolismo
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