Abstract/Details

Locating Binding Sites of the General Anaesthetic Propofol Using Photoaffinity Labelling

Yip, Grace Mei Shan.   Imperial College London (United Kingdom) ProQuest Dissertations & Theses,  2013. U615113.

Abstract (summary)

3-(5'-isopropyl-6'-hydroxyphenyl)-3-trifluoromethyl-diazirine (photofol), a new drug developed in our laboratory, is structurally homologus to the general anaesthetic propofol with one of its isopropyl groups being substituted for a trifluoromethyl-diazirine group. Photofol was shown to act in a similar manner to propofol, albeit with a three-fold reduction in potency on inducing a loss of righting reflex in rats and with reduced modulation of GABA-evoked currents on α1 β2 γ2s GABAA receptors for the concentration tested. The soluble protein human serum albumin (HSA) and the pentameric ligand-gated ion channel GLIC from the prokaryote Gloeobacter violaceus were used to test the utility of photofol as a photoaffinity label. Both proteins have been crystallised with propofol to produce high-resolution X-ray structures (Bhattacharya et al., 2000; Nury et al., 2011). Two samples of the photolabel—one containing naturally occurring hydrogen atoms and the other a bespoke proportion of different isotopes with between zero and two deuterium atoms—were used and this novel approach was successfully demonstrated to aid the analysis of mass spectra through their differences in isotopic distribution. Photolabelling HSA and GLIC followed by enzyme cleavage, liquid chromatography-mass spectrometry and tandem mass spectrometry identified the binding of photofol to six different amino acids. Photofol labelled all three protofol-binding sites of HSA identified by X-ray crystallography. Peptides that are part of the propofol-binding site in the GLIC transmembrane domain reduced in ionisation intensity upon photolabelling, suggesting that photofol had bound to this vicinity. Furthermore, photolabelling of binding sites at the interfaces between subunits in the extracellular domain was reproducibly observed, particularly at lysine-183. Electrophysiology-couple mutagenesis studies are currently underway to confirm to propofol binding to the site, where binding to another general anaesthetic, ketamine, has recently been shown by high-resolution structures (Pan et al., 2012a). In conclusion, the work presented herein indicates that photofol is a suitable photolabel for locating for locating binding sites of propofol.

Indexing (details)


Subject
Nursing
Classification
0569: Nursing
Identifier / keyword
(UMI)AAIU615113; Health and environmental sciences
Title
Locating Binding Sites of the General Anaesthetic Propofol Using Photoaffinity Labelling
Author
Yip, Grace Mei Shan
Number of pages
1
Degree date
2013
School code
8350
Source
DAI-C 73/12, Dissertation Abstracts International
University/institution
Imperial College London (United Kingdom)
University location
England
Degree
Ph.D.
Source type
Dissertation or Thesis
Language
English
Document type
Dissertation/Thesis
Note
Bibliographic data provided by EThOS, the British Library’s UK thesis service: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.570074
Dissertation/thesis number
U615113
ProQuest document ID
1557542738
Copyright
Database copyright ProQuest LLC; ProQuest does not claim copyright in the individual underlying works.
Document URL
https://www.proquest.com/docview/1557542738/abstract/