Scattering from biopolymers with helical symmetry in solution

Small angle X‐ray fibre diffraction on aligned elongated macromolecules has been a routine tool for the structure of materials that either can not be crystallized or in cases in which one wants to study the structure of the molecule as close as possible to those occurring in solution. One of the pro...

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Bibliographic Details
Published inJournal of applied crystallography Vol. 33; no. 3-1; pp. 659 - 663
Main Authors Bras, W., Diakun, G.P., Denny, R.C., Ferrero, C., Levine, Y.K., Dìaz, F.
Format Journal Article Conference Proceeding
LanguageEnglish
Published 5 Abbey Square, Chester, Cheshire CH1 2HU, England Munksgaard International Publishers 01.06.2000
Blackwell
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Summary:Small angle X‐ray fibre diffraction on aligned elongated macromolecules has been a routine tool for the structure of materials that either can not be crystallized or in cases in which one wants to study the structure of the molecule as close as possible to those occurring in solution. One of the problems with this approach is that quite often it is not possible to obtain completely aligned samples but only samples in which there is an angular distribution around the main orientation axis. This has as a consequence that atlarger scattering angles the contributions from different layer lines start to overlap. A possible method to overcome this problem can be found in combining results from small angle solution scattering with small angle fibre diffraction from molecules aligned with their long axis parallel with respect to the X‐ray beam. In the latter case one only observes the projection of the molecule on the basal plane. We show how this method can be applied to hydrated microtubules.
Bibliography:ark:/67375/WNG-VF3MMXH2-7
istex:39D4AEF14EDC02A4E6096EFCECBCA16BB14828B6
ArticleID:JCRHS2095
ISSN:1600-5767
0021-8898
1600-5767
DOI:10.1107/S002188989901328X