The immunoPeptidoGenomic (iPepGen) informatics resource forimmuno-oncology research
- Institution
- UNIVERSITY OF MINNESOTA, MN
- Principal investigator
- Timothy J. Griffin
- Funding
- $387K
- Duration
- 2024–2027
Moonbase score
Still being scored
Abstract
SUMMARY Immuno-oncology studies continue to grow which seek new therapies leveraging immunogenic, non-normal peptide sequences (neoantigens) arising from tumor-specific alterations at the genomic, transcriptomic or proteomic level. Non-normal DNA and RNA sequences that may encode neoantigens can be identified from next-generation sequencing (NGS) data, and further prioritized by their predicted binding to the class I or II major histocompatibility complex (MHC) as an indicator of immunogenicity. Immunopeptidomic enrichment of the peptide-MHC complex coupled with liquid chromatography tandem mass spectrometry (LC-MS/MS) can confirm the existence of predicted neoantigens as well as other tumor-associated antigens (TAAs) derived from normal protein sequences, including those with post-translational modifications (PTMs). This powerful approach requires `immunopeptidogenomic' informatics tools that integrate NGS and MS data analysis. Despite steadily growing numbers of cancer researchers pursuing these studies, they lack a centralized informatics resource tailored to these informatics requirements. As a solution, we will develop the immunopeptidogenomic (iPepGen) informatics resource for immuno-oncology research. iPepGen will leverage the Galaxy bioinformatics ecosystem, offering cancer researchers accessible workflows to predict neoantigens from NGS data and confirm their presence from MS-based immunopeptidomics data, including training resources housed in the Galaxy Training Network to promote community adoption. We will achieve our goals through these Specific Aims: Aim 1: Optimize and harden modular workflows for identifying, prioritizing and curating neoantigen candidates detected from genomic and/or transcriptomic alterations; Aim 2: Optimize and harden state-of-the-art MS-based immunopeptidomic analysis modules for identifying and verifying MHC-bound neoantigen and TAA peptides; Aim 3: Disseminate tested and optimized workflows and engage in training activities to promote community adoption of the iPepGen resource. Our team brings complementary, world-class expertise necessary for success in developing the iPepGen resource. PIs Griffin and Jagtap have developed widely used Galaxy-based multi-omic tools and training materials for cancer research. PI Nesvizhskii is a world-leader in development of computational tools for quantitative, MS-based proteomic and peptidomic analysis. Development, testing and optimization of tools, workflows and training materials will be guided by collaboration with cancer researchers conducting Driving Immuno-oncology Projects (DIPs). The iPepGen resource will offer a critically needed resource to advance game-changing immunotherapy studies impacting a wide-variety of cancer types.
Research team
- Timothy J. GriffinPI
- Pratik D JagtapPI
- Alexey I NesvizhskiiPI
LOADING MOONBASE SCORE
Questions for UNIVERSITY OF MINNESOTA
Answered by the team behind this research.
No questions yet. Sign in to ask the first one
Related grants
Same researchers, same institution, same topic, scored first.
- NIH · University of MinnesotaNot yet scored
An enabling approach for deep metaproteomic characterization ofmicrobial contributors to tumorigenesis in clinical samples
Timothy J. Griffin · $221K · 2025–2028
- NIH · University of MinnesotaNot yet scored
Proteogenomics Shared Resource
Timothy J. Griffin · $111K · 1998–2029
- NIH · University of Minnesota73
Development and Translation of an Intracranial Auditory Nerve Implant
Meredith Evelyn Adams · $1.5M · 2018–2027