演題概要

ポスター発表

第1日 5月17日(水)  P会場(多目的ホール)

創薬ターゲット化合物スクリーニングを目指した質量分析による分子間相互作用解析技術の開発

(1バイオシス2日本写真印刷3聖マリ医4Silicon Kinetics5東大院工・東大創薬6東大アイソトープ)
o福田哲也1小尾奈緒子2中山登1,3John, Ervin4板東泰彦1西村俊秀1,3染原俊朗2長門石曉5津本浩平5川村猛6

The nano Pore Optical Interferometry (nPOI) can measure a Kon/Koff histogram on binding kinetics of molecular species in the same manner as SPR, and can identify and quantify compounds/biomolecules even weakly interacting in a complex mixture by mass spectrometry. The nPOI is in principle different from surface plasmon resonance (SPR), and is highly advantageous in its capacity to capture binding molecules 100 times more than the conventional SPR methods, and that nPOI therefore makes it possible to identify weakly interacting molecules which are useful in designing fragment-based and/or medium-size molecules-based drug developments1). In our research group, Carbonic Anhydrase II was immobilized as a ligand protein to the sensor cartridge, six types of low molecular model compounds were applied as analyte, then affinity analysis was performed, and eluted compounds were introduced to nano-ESI LC-MS for verification.