A new method for fibrous protein analysis illustrated by application to tubulin microtubule polymerisation and depolymerisation

dc.contributor.authorMarrington, Rachelen
dc.contributor.authorSeymour, Marken
dc.contributor.authorRodger, Alisonen
dc.date.accessioned2026-01-01T12:42:19Z
dc.date.available2026-01-01T12:42:19Z
dc.date.issued2006en
dc.description.abstractA thermostatted micro volume Couette cell has been designed to enable linear dichroism (LD) data to be collected at a range of temperatures. The cell is a development of the traditional Couette flow LD cell and includes the recent development of micro-volume LD (20-40 μL) coupled with the addition of a heating element, temperature probe and controller. This new micro volume Couette LD cell opens the way not only to the LD analysis of systems where sample volume is critical, but also for the LD analysis of temperature sensitive samples. The polymerization of the microtubule protein tubulin has been followed in a range of different conditions using the thermostatted micro volume Couette LD cell. The focusing lenses on the cell, which are required for the microvolume cell, have the side benefit of significantly reducing the light-scattering artifacts caused by the large size of tubulin microtubules. It is now possible to monitor real-time polymerization and depolymerization kinetics, and any structural rearrangements of chromophores within the polymer. In the case of tubulin, the LD spectra revealed a greater change in the orientation of tryptophan residues at ∼290 nm during polymerization compared to other contributing chromophores-guanine, phenylalanine, and tyrosine. The improvements in instrumental design have also allowed LD spectra of tubulin to be collected down to ∼230 nm (previous data have only been available from the near UV region), which means that some indication of protein backbone-orientation changes are now available. It was observed during this work that apparent LD intensity maxima are in fact artifacts when the high-tension voltage is high. The onset of such artifacts has been observed at much lower voltages with light-scattering fibrous proteins (including tubulin) than with nonscattering samples. Therefore, caution must be used when interpreting LD data collected with medium to high photomultiplier tube voltages.en
dc.description.statusPeer-revieweden
dc.format.extent11en
dc.identifier.issn0899-0042en
dc.identifier.otherPubMed:16823813en
dc.identifier.otherORCID:/0000-0002-7111-3024/work/162949318en
dc.identifier.scopus33748801723en
dc.identifier.urihttps://hdl.handle.net/1885/733800443
dc.language.isoenen
dc.sourceChiralityen
dc.subjectCouetteen
dc.subjectDepolymerizationen
dc.subjectKineticsen
dc.subjectLinear dichroismen
dc.subjectMicrovolumeen
dc.subjectPolymerizationen
dc.subjectThermostatteden
dc.subjectTubulinen
dc.titleA new method for fibrous protein analysis illustrated by application to tubulin microtubule polymerisation and depolymerisationen
dc.typeJournal articleen
dspace.entity.typePublicationen
local.bibliographicCitation.lastpage690en
local.bibliographicCitation.startpage680en
local.contributor.affiliationMarrington, Rachel; University of Warwicken
local.contributor.affiliationSeymour, Mark; Syngentaen
local.contributor.affiliationRodger, Alison; University of Warwicken
local.identifier.citationvolume18en
local.identifier.doi10.1002/chir.20305en
local.identifier.pure2fa191bf-6ae0-46fa-9fd7-b2779075400fen
local.identifier.urlhttps://www.scopus.com/pages/publications/33748801723en
local.type.statusPublisheden

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