Deep learning based antibody design using high-throughput affinity testing of synthetic sequences
Deep learning based antibody design using high-throughput affinity testing of synthetic sequences
批准号:
10116306
负责人:
David K Gifford
金额:
$59.11万
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-03-09 至 2024-02-28
关键词:
AffinityAnimalsAntibodiesAntibody AffinityAntigensArchitectureBindingBiological AssayBudgetsClassificationCloud ComputingCommunicable DiseasesComputing MethodologiesDNA SequenceDataData SetDiseaseFc ReceptorGoalsHumanImmunizeImmunotherapeutic agentLearningMachine LearningMalignant NeoplasmsMethodologyMethodsModelingMolecular MachinesOligonucleotidesOutputPerformancePhage DisplayPropertyRandomizedResearchServicesSpecific qualifier valueSpecificityStatistical ModelsTechnologyTest ResultTestingTherapeuticThinnessTimeTrainingTreatment EfficacyUpdateVirus DiseasesWorkantibody testbasecloud basedcommercializationcomputing resourcescostdeep learningdesignexperimental studyhuman diseaseimprovediterative designlearning strategymachine learning methodmathematical methodsmolecular dynamicsnovelnovel strategiesoutcome predictionpredictive testreceptor
中文摘要
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英文摘要
Project Summary
We will develop and apply a new high-throughput methodology for rapidly
designing and testing antibodies for a myriad of purposes, including cancer and
infectious disease immunotherapeutics. We will improve upon current
approaches for antibody design by providing time, cost, and humane benefits
over immunized animal methods and greatly improving the power of present
synthetic methods that use randomized designs. To accomplish this, we will
display millions of computationally designed antibody sequences using recently
available technology, test the displayed antibodies in a high-throughput format at
low cost, and use the resulting test data to train molecular dynamics and
machine learning methods to generate new sequences for testing. Based on our
test data our computational method will identify sequences that have ideal
properties for target binding and therapeutic efficacy. We will accomplish these
goals with three specific aims. We will develop a new approach to integrated
molecular dynamics and machine learning using control targets and known
receptor sequences to refine our methods for receptor generalization and model
updating from observed data (Aim 1). We will design an iterative framework
intended to enable identification of highly effective antibodies within a minimal
number of experiments, in which our methods automatically propose promising
antibody sequences to profile in subsequent assays (Aim 2). We will employ
rounds of automated synthetic design, affinity test, and model improvement to
produce highly target-specific antibodies. (Aim 3).
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海外基金