ACE
ACE optimizes pooled ELISpot assay design and deconvolution using a fine-tuned ESM-2 sequence-aware peptide clustering to improve identification of antigen-specific immunogenic peptides.
Key Features:
- Sequence-Aware Pooling Strategy: Uses a fine-tuned ESM-2 model to cluster peptides by immunological similarity and inform peptide-pool assignments.
- Customizable Assay Design: Accepts user-defined parameters to generate optimized peptide-pool assignments tailored to experimental requirements.
- Efficient Deconvolution of Pool Spot Counts: Implements a deconvolution algorithm that processes ELISpot readouts to identify immunogenic peptides from positive pools.
- High-Throughput Capability: Supports scalable pooled ELISpot designs intended for large-scale studies and high-throughput screening.
Scientific Applications:
- Epitope immunogenicity validation: Validates predicted epitopes by identifying immunogenic peptides from pooled ELISpot data.
- Cancer immunology: Applies optimized pooled ELISpot designs to quantify antigen-specific T-cell reactivity in cancer research.
- Infectious disease immunology: Applies optimized pooled ELISpot designs to quantify antigen-specific T-cell reactivity in infectious disease research.
- High-throughput peptide screening: Enables large-scale identification of immunogenic peptides from complex peptide sets.
Methodology:
Peptides are clustered by a fine-tuned ESM-2 model to inform sequence-aware pooling, and a deconvolution algorithm processes ELISpot spot counts to pinpoint immunogenic peptides.
Topics
Details
- License:
- Apache-2.0
- Cost:
- Free of charge
- Tool Type:
- command-line tool, library
- Programming Languages:
- JavaScript, Python
- Added:
- 5/24/2024
- Last Updated:
- 11/24/2024
Operations
Publications
Lee JS, Karthikeyan D, Fini M, Vincent BG, Rubinsteyn A. ACE configurator for ELISpot: optimizing combinatorial design of pooled ELISpot assays with an epitope similarity model. Briefings in Bioinformatics. 2023;25(1). doi:10.1093/bib/bbad495. PMID:38180831. PMCID:PMC10768796.
DOI: 10.1093/bib/bbad495
PMID: 38180831
PMCID: PMC10768796
Funding: - National Institutes of Health Clinical Center: R37CA247676
- National Institutes of Health: T32GM008570-28
- National Science Foundation: DGE-2040435