A cell-based screening method using an intracellular antibody for discovering small molecules targeting the translocation protein LMO2

被引:9
作者
Bery, Nicolas [1 ,4 ]
Bataille, Carole J. R. [2 ,4 ]
Russell, Angela [2 ]
Hayes, Angela [3 ]
Raynaud, Florence [3 ]
Milhas, Sabine [1 ,5 ]
Anand, Sneha [1 ]
Tulmin, Hanna [1 ,6 ,7 ]
Miller, Ami [1 ,8 ]
Rabbitts, Terence H. [1 ,8 ]
机构
[1] Univ Oxford, Weatherall Inst Mol Med, MRC Mol Haematol Unit, John Radcliffe Hosp, Oxford OX3 9DS, England
[2] Univ Oxford, Chem Res Lab, Oxford OX1 3TA, England
[3] Inst Canc Res, 15 Cotswold Rd, London SM2 5NG, England
[4] Univ Toulouse III Paul Sabatier, Canc Res Ctr Toulouse, CNRS, INSERM, Toulouse, France
[5] Vertex Pharmaceut, 88 Jubilee Ave, Milton Pk OX14 4RW, England
[6] Univ Oxford, Nuffield Dept Med, Wellcome Ctr Human Genet, JDRF Wellcome Diabet & Inflammat Lab, Oxford OX3 7BN, England
[7] Czech Acad Sci, Inst Organ Chem & Biochem, Flemingovo Namesti 542-2, Prague 16000 6, Czech Republic
[8] Inst Canc Res, Div Canc Therapeut, 15 Cotswold Rd, London SM2 5NG, England
基金
英国惠康基金;
关键词
Antibodies;
D O I
10.1126/sciadv.abg1950
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Intracellular antibodies are tools that can be used directly for target validation by interfering with properties like protein-protein interactions. An alternative use of intracellular antibodies in drug discovery is developing small-molecule surrogates using antibody-derived (Abd) technology. We previously used this strategy with an in vitro competitive surface plasmon resonance method that relied on high-affinity antibody fragments to obtain RAS-binding compounds. We now describe a novel implementation of the Abd method with a cell-based intracellular antibody-guided screening method that we have applied to the chromosomal translocation protein LMO2. We have identified a chemical series of anti-LMO2 Abd compounds that bind at the same LMO2 location as the inhibitory anti-LMO2 intracellular antibody combining site. Intracellular antibodies could therefore be used in cell-based screens to identify chemical surrogates of their binding sites and potentially be applied to any challenging proteins, such as transcription factors that have been considered undruggable.
引用
收藏
页数:14
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