第72回 アイセムスセミナー / CeMI セミナーシリーズ 22: Simon Davis 教授

CeMICenter for Meso-Bio Single-Molecule Imaging

The T cell receptor (TCR) was discovered over 25 years ago but it is still notclear how it is "triggered" i.e. it conveys information about ligand binding at the cell surface to the interior of the T cell. Prof. Davis' group proposes that conventional theories of autonomous receptor triggering are incompatible with what they know about the structure of the TCR or how it functions. Prof. Davis will present an analysis of the architecture of the triggering apparatus of the T cell based on two-colour coincidence detection (a form of single-molecule confocal microscopy). He will then propose a mechanism for TCR triggering wherein, rather than functioning autonomously, the TCR behaves as a passive structure subject to the ensemble behaviour of extrinsic tyrosine kinases and phosphatases. He will also describe how his group is trying to verify the theory using single-molecule and other imaging approaches, and will extend the concept to a consideration of the effects of superagonistic antibodies, based on the crystal structure of an antibody superagonist bound to its cellular target. Finally, Prof. Davis will discuss how, in general terms, the artificial triggering of inhibitory receptors could be employed for therapeutic ends.

講演者
演題
Prof. Simon Davis
Nuffield Department of Clinical Medicine
英国 オックスフォード大学
演題:The T-cell surface: composition, organization, receptor triggering
日時 2011年3月17日(木)10:00-11:00
場所 京都大学 再生医科学研究所 東館5階ルーフテラス
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主催 京都大学 物質-細胞統合システム拠点(iCeMS=アイセムス)
連絡先 iCeMS 楠見明弘 / Fax: 075-751-4113
akusumi@frontier.kyoto-u.ac.jp