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Separating nucleation and growth in protein crystallization using dynamic light scattering.
Saridakis, Emmanuel; Dierks, Karsten; Moreno, Abel; Dieckmann, Matthias W M; Chayen, Naomi E.
Afiliação
  • Saridakis E; Biological Structure and Function Section, Division of Biomedical Sciences, Faculty of Medicine, Imperial College, London SW7 2AZ, UK.
Acta Crystallogr D Biol Crystallogr ; 58(Pt 10 Pt 1): 1597-600, 2002 Oct.
Article em En | MEDLINE | ID: mdl-12351869
ABSTRACT
A means of controlling crystallization is to separate the phases of nucleation and growth. Methods to achieve this, other than seeding, involve lowering the supersaturation by changing the temperature or diluting drops after incubating them for a given time at nucleation conditions. However, by the time nuclei or crystals are visible under the microscope too many nuclei will have formed. Dynamic Light Scattering was applied practically, to determine the most likely time for nucleation-growth decoupling to be performed successfully. The time at which DLS showed a significant change in the size-distribution of species in solution, corresponded to that optimal time.
Assuntos
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Base de dados: MEDLINE Assunto principal: Proteínas / Cristalização Limite: Animals Idioma: En Ano de publicação: 2002 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Proteínas / Cristalização Limite: Animals Idioma: En Ano de publicação: 2002 Tipo de documento: Article