An ultra-high-throughput screen for the evaluation of peptide HLA-Binder interactions

被引:3
作者
Kraemer, Stefan [1 ]
Moritz, Andreas [3 ]
Stehl, Luca [1 ]
Hutt, Meike [3 ]
Hofmann, Martin [3 ]
Wagner, Claudia [3 ]
Bunk, Sebastian [3 ]
Maurer, Dominik [3 ]
Roth, Guenter [1 ,2 ]
Woehrle, Johannes [1 ]
机构
[1] BioCopy GmbH, D-79312 Emmendingen, Germany
[2] BioCopy AG, CH-4123 Basel, Switzerland
[3] Immatics Biotechnol GmbH, D-72076 Tubingen, Germany
关键词
LABEL-FREE DETECTION; BIOMOLECULAR INTERACTIONS; CANCER REGRESSION; INTERFEROMETRY; MICROARRAYS; TOXICITY; AFFINITY; PLATFORM; THERAPY;
D O I
10.1038/s41598-023-32384-z
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
Peptide human leukocyte antigen (pHLA) targeting therapeutics like T-cell receptor based adoptive cell therapy or bispecific T cell engaging receptor molecules hold great promise for the treatment of cancer. Comprehensive pre-clinical screening of therapeutic candidates is important to ensure patient safety but is challenging because of the size of the potential off-target space. By combining stabilized peptide-receptive HLA molecules with microarray printing and screening, we have developed an ultra-high-throughput screening platform named ValidaTe that enables large scale evaluation of pHLA-binder interactions. We demonstrate its potential by measuring and analyzing over 30.000 binding curves for a high-affinity T cell Engaging Receptor towards a large pHLA library. Compared to a dataset obtained by conventional bio-layer interferometry measurements, we illustrate that a massively increased throughput (over 650 fold) is obtained by our microarray screening, paving the way for use in pre-clinical safety screening of pHLA-targeting drugs.
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页数:8
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