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1.
Acta Crystallogr D Biol Crystallogr ; 69(Pt 8): 1617-32, 2013 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-23897484

RESUMO

The availability of intense microbeam macromolecular crystallography beamlines at third-generation synchrotron sources has enabled data collection and structure solution from microcrystals of <10 µm in size. The increased likelihood of severe radiation damage where microcrystals or particularly sensitive crystals are used forces crystallographers to acquire large numbers of data sets from many crystals of the same protein structure. The associated analysis and merging of multi-crystal data is currently a manual and time-consuming step. Here, a computer program, BLEND, that has been written to assist with and automate many of the steps in this process is described. It is demonstrated how BLEND has successfully been used in the solution of a novel membrane protein.


Assuntos
Análise por Conglomerados , Cristalografia por Raios X/métodos , Software , Insulina/química , Proteínas de Membrana/química , Modelos Moleculares , Muramidase , Proteínas de Plantas/química , Síncrotrons , Temperatura
2.
Acta Crystallogr D Biol Crystallogr ; 69(Pt 7): 1252-9, 2013 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-23793151

RESUMO

The focus in macromolecular crystallography is moving towards even more challenging target proteins that often crystallize on much smaller scales and are frequently mounted in opaque or highly refractive materials. It is therefore essential that X-ray beamline technology develops in parallel to accommodate such difficult samples. In this paper, the use of X-ray microradiography and microtomography is reported as a tool for crystal visualization, location and characterization on the macromolecular crystallography beamlines at the Diamond Light Source. The technique is particularly useful for microcrystals and for crystals mounted in opaque materials such as lipid cubic phase. X-ray diffraction raster scanning can be used in combination with radiography to allow informed decision-making at the beamline prior to diffraction data collection. It is demonstrated that the X-ray dose required for a full tomography measurement is similar to that for a diffraction grid-scan, but for sample location and shape estimation alone just a few radiographic projections may be required.


Assuntos
Bacteriorodopsinas/química , Processamento de Imagem Assistida por Computador , Lipídeos/química , Microrradiografia , Nitrito Redutases/química , Receptor A2A de Adenosina/química , Tomografia Computadorizada por Raios X , Algoritmos , Cristalografia por Raios X , Interpretação Estatística de Dados , Processamento Eletrônico de Dados , Humanos , Software
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