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1.
Phys Rev Lett ; 120(21): 211804, 2018 May 25.
Artigo em Inglês | MEDLINE | ID: mdl-29883176

RESUMO

The Majorana Demonstrator is an ultralow-background experiment searching for neutrinoless double-beta decay in ^{76}Ge. The heavily shielded array of germanium detectors, placed nearly a mile underground at the Sanford Underground Research Facility in Lead, South Dakota, also allows searches for new exotic physics. Free, relativistic, lightly ionizing particles with an electrical charge less than e are forbidden by the standard model but predicted by some of its extensions. If such particles exist, they might be detected in the Majorana Demonstrator by searching for multiple-detector events with individual-detector energy depositions down to 1 keV. This search is background-free, and no candidate events have been found in 285 days of data taking. New direct-detection limits are set for the flux of lightly ionizing particles for charges as low as e/1000.

2.
Eur Phys J C Part Fields ; 82(3): 226, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35310515

RESUMO

P-type point contact (PPC) HPGe detectors are a leading technology for rare event searches due to their excellent energy resolution, low thresholds, and multi-site event rejection capabilities. We have characterized a PPC detector's response to α particles incident on the sensitive passivated and p + surfaces, a previously poorly-understood source of background. The detector studied is identical to those in the Majorana Demonstrator experiment, a search for neutrinoless double-beta decay ( 0 ν ß ß ) in 76 Ge. α decays on most of the passivated surface exhibit significant energy loss due to charge trapping, with waveforms exhibiting a delayed charge recovery (DCR) signature caused by the slow collection of a fraction of the trapped charge. The DCR is found to be complementary to existing methods of α identification, reliably identifying α background events on the passivated surface of the detector. We demonstrate effective rejection of all surface α events (to within statistical uncertainty) with a loss of only 0.2% of bulk events by combining the DCR discriminator with previously-used methods. The DCR discriminator has been used to reduce the background rate in the 0 ν ß ß region of interest window by an order of magnitude in the Majorana Demonstrator  and will be used in the upcoming LEGEND-200 experiment.

3.
Curr Opin Cell Biol ; 6(1): 87-95, 1994 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-8167031

RESUMO

The three-dimensional structures of myosin subfragment 1 (S1), gelsolin segment 1 complexed with alpha-actin, villin fragment 14T, Acanthamoeba profilin-I, and bovine profilin complexed with beta-actin were completed last year. Together, they expand our understanding of the structural organization of actin-binding proteins. In addition, the segment 1 and bovine profilin complexes provide atomic-level descriptions of their interfaces with actin.


Assuntos
Actinas/química , Proteínas dos Microfilamentos/química , Estrutura Secundária de Proteína , Actinas/metabolismo , Sequência de Aminoácidos , Animais , Sítios de Ligação , Proteínas de Transporte/química , Proteínas de Transporte/metabolismo , Gelsolina/química , Gelsolina/metabolismo , Humanos , Proteínas dos Microfilamentos/metabolismo , Modelos Moleculares , Dados de Sequência Molecular , Subfragmentos de Miosina/química , Subfragmentos de Miosina/metabolismo
4.
J Mol Biol ; 209(4): 735-46, 1989 Oct 20.
Artigo em Inglês | MEDLINE | ID: mdl-2585507

RESUMO

Analysis of profilin: actin crystals reveals an extensive intermolecular network, rather than a discrete "monomeric complex", comprising stacked actin ribbons held in place by columns of profilin molecules, wedged in between neighboring actin subunits and running perpendicular to the ribbons. Comparison with data from electron microscopy, X-ray diffraction, spectroscopy, and biochemistry of actin suggests that a simple transformation relates the ribbon to f-actin. The crystals exhibit unusual polymorphic properties, which strengthens the view that movements within the actin monomer are important for force generation.


Assuntos
Actinas/análise , Proteínas Contráteis , Proteínas dos Microfilamentos/análise , Actinas/ultraestrutura , Trifosfato de Adenosina/metabolismo , Cristalização , Cristalografia , Contração Muscular , Profilinas , Conformação Proteica
5.
J Mol Biol ; 240(5): 459-75, 1994 Jul 29.
Artigo em Inglês | MEDLINE | ID: mdl-8046751

RESUMO

Profilin regulates the behavior of the eukaryotic microfilament system through its interaction with non-filamentous actin. It also binds several ligands, including poly(L-proline) and the membrane phospholipid phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2). Bovine profilin crystals (space group C2; a = 69.15 A, b = 34.59 A, c = 52.49 A; alpha = gamma = 90 degrees, beta = 92.56 degrees) were grown from a mixture of poly(ethylene glycol) 400 and ammonium sulfate. X-ray diffraction data were collected on an imaging plate scanner at the DORIS storage ring (DESY, Hamburg), and were phased by molecular replacement, using a search model derived from the 2.55 A structure of profilin complexed to beta-actin. The refined model of bovine profilin has a crystallographic R-factor of 16.5% in the resolution range 6.0 to 2.0 A and includes 128 water molecules, several of which form hydrogen bonds to stabilize unconventional turns. The structure of free bovine profilin is similar to that of bovine profilin complexed to beta-actin, and C alpha atoms from the two structures superimpose with an r.m.s. deviation of 1.25 A. This value is reduced to 0.51 A by omitting Ala1 and the N-terminal acetyl group, which lie at a profilin-actin interface in crystals of the complex. These residues display a strained conformation in crystalline profilin-actin but may allow the formation of a hydrogen bond between the N-acetyl carbonyl group of profilin and the phenol hydroxyl group of Tyr188 in actin. Several other actin-binding residues of profilin show different side-chain rotomer conformations in the two structures. The polypeptide fold of bovine profilin is generally similar to those observed by NMR for profilin from other sources, although the N terminus of Acanthamoeba profilin isoform I lies in a distorted helix and the C-terminal helix is less tilted with respect to the strands in the central beta-pleated sheet than is observed in bovine profilin. The majority of the aromatic residues in profilin are exposed to solvent and lie in either of two hydrophobic patches, neither of which takes part in an interface with actin. One of these patches is required for binding poly(L-proline) and contains an aromatic cluster comprising the highly conserved residues Trp3, Tyr6, Trp31 and Tyr139. In forming this cluster, Trp31 adopts a sterically strained rotamer conformation.(ABSTRACT TRUNCATED AT 400 WORDS)


Assuntos
Proteínas Contráteis , Proteínas dos Microfilamentos/química , Estrutura Secundária de Proteína , Actinas/metabolismo , Sequência de Aminoácidos , Aminoácidos/análise , Animais , Sítios de Ligação , Bovinos , Cristalização , Cristalografia por Raios X , Ligação de Hidrogênio , Proteínas dos Microfilamentos/metabolismo , Modelos Moleculares , Dados de Sequência Molecular , Estrutura Molecular , Profilinas , Dobramento de Proteína , Alinhamento de Sequência , Água/química
6.
J Biomol Screen ; 6(6): 429-40, 2001 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-11788061

RESUMO

More general and universally applicable drug discovery assay technologies are needed in order to keep pace with the recent advances in combinatorial chemistry and genomics-based target generation. Ligand-induced conformational stabilization of proteins is a well-understood phenomenon in which substrates, inhibitors, cofactors, and even other proteins provide enhanced stability to proteins on binding. This phenomenon is based on the energetic coupling of the ligand-binding and protein-melting reactions. In an attempt to harness these biophysical properties for drug discovery, fully automated instrumentation was designed and implemented to perform miniaturized fluorescence-based thermal shift assays in a microplate format for the high throughput screening of compound libraries. Validation of this process and instrumentation was achieved by investigating ligand binding to more than 100 protein targets. The general applicability of the thermal shift screening strategy was found to be an important advantage because it circumvents the need to design and retool new assays with each new therapeutic target. Moreover, the miniaturized thermal shift assay methodology does not require any prior knowledge of a therapeutic target's function, making it ideally suited for the quantitative high throughput drug screening and evaluation of targets derived from genomics.


Assuntos
Miniaturização , Preparações Farmacêuticas/química , Receptor alfa de Estrogênio , Corantes Fluorescentes , Humanos , Ligantes , Proteínas/metabolismo , Receptores de Estrogênio/metabolismo , Reprodutibilidade dos Testes , Temperatura
7.
Mol Divers ; 4(1): 1-22, 1998.
Artigo em Inglês | MEDLINE | ID: mdl-10320984

RESUMO

Rapid advances in synthetic and screening technology have recently enabled the simultaneous synthesis and biological evaluation of large chemical libraries containing hundreds to tens of thousands of compounds, using molecular diversity as a means to design and prioritize experiments. This paper reviews some of the most important computational work in the field of diversity profiling and combinatorial library design, with particular emphasis on methodology and applications. It is divided into four sections that address issues related to molecular representation, dimensionality reduction, compound selection, and visualization.


Assuntos
Química Farmacêutica/métodos , Biblioteca de Peptídeos , Simulação por Computador , Desenho de Fármacos , Modelos Químicos , Modelos Estatísticos , Software
8.
Nature ; 365(6449): 810-6, 1993 Oct 28.
Artigo em Inglês | MEDLINE | ID: mdl-8413665

RESUMO

The three-dimensional structure of bovine profilin-beta-actin has been solved to 2.55 A resolution by X-ray crystallography. There are several significant local changes in the structure of beta-actin compared with alpha-actin as well as an overall 5 degrees rotation between its two major domains. Actin molecules in the crystal are organized into ribbons through intermolecular contacts like those found in oligomeric protein assemblies. Profilin forms two extensive contacts with the actin ribbon, one of which appears to correspond to the solution contact in vitro.


Assuntos
Proteínas Contráteis , Proteínas dos Microfilamentos/química , Proteínas/química , Actinas , Sequência de Aminoácidos , Animais , Bovinos , Gráficos por Computador , Cristalografia por Raios X , Humanos , Proteínas dos Microfilamentos/fisiologia , Dados de Sequência Molecular , Profilinas , Ligação Proteica , Conformação Proteica
9.
Nature ; 353(6344): 508, 1991 Oct 10.
Artigo em Inglês | MEDLINE | ID: mdl-1922357
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