Next-generation oncoproteomic sequencing and precision profiling
Active Project Grant Awarded Last action
- Award ID
- R21CA304932
- Recipient
-
Electronic Biosciences, Inc. UEI FLHHE89XH2H5
- Awarding agency
-
National Cancer Institute
National Institutes of Health, Department of Health and Human Services
- Obligated
- $418,854
Award facts
- Assistance listing
- 93.396 Cancer Biology Research
- Completion date 19% complete
- Place of performance
- Emigration Canyon, UT 84108, USA
Award details come from USAspending.gov.
About this award
The National Cancer Institute awarded Electronic Biosciences, Inc. $418,854 on June 8, 2026, under the Cancer Biology Research program (CFDA 93.396) to develop a next-generation single-molecule protein sequencing platform for oncoproteomic analysis.
The project delivers a nanopore-based sequencing system capable of directly sequencing individual proteins, identifying variants, and profiling post-translational modifications such as phosphorylation and glycosylation. The platform addresses limitations in current protein analysis technologies by enabling repeated sequencing of the same protein molecule to generate high-accuracy consensus sequences, providing single-molecule coverage for ultra-precise detection of protein variants and cancer-related modifications central to oncogenic processes.
Electronic Biosciences is a San Diego-based for-profit biotechnology company specializing in nanopore-based sequencing and diagnostic platforms. The company operates exclusively as a prime recipient of federal grants under SBIR and STTR programs across the National Institutes of Health ecosystem.
Period of performance runs through May 31, 2028. Place of performance is Emigration Canyon, Utah 84108.
Description
- Abstract
- Proteins are the essential workhorses of the cell, driving nearly every biological process. Their complex interactions, alterations, and post-translational modifications (ptms) play critical roles in cancer development and progression. However, current protein analysis technologies suffer from significant limitations in sensitivity, accuracy, and throughput, hindering a comprehensive understanding of the proteomic landscape of cancer. There is an urgent need for a platform that can directly and accurately sequence individual proteins, identify variants, and profile complex modifications like phosphorylation and glycosylation, which are central to oncogenic processes. To address these limitations, we propose to develop an entirely new single-molecule protein sequencing platform capable of manipulating, controlling, and iteratively RE-sequencing individual proteins. Our technology represents a transformative advance in oncoproteomics by offering direct, high-accuracy protein sequencing, overcoming the low throughput and labor-intensive nature of existing methods. By repeatedly sequencing the same protein molecule, our system provides unlimited coverage at the single-molecule level, enabling ultra-precise identification of protein variants and ptms. This approach is essential for detecting single- point mutations and profiling cancer-related proteins with unprecedented accuracy. Our platform will leverage proven nanopore sequencing strategies adapted specifically for protein sequencing. The technology integrates multiple controllable methods to linearize proteins and control their movement through the nanopore, generating detailed current-time signatures for each amino acid. By controlling the translocation velocity and RE-sequencing the same protein multiple times, we can construct high-accuracy consensus sequences, offering a gold-standard tool for oncoproteomic research. In this project, we will develop and optimize a 4-plex sequencing system capable of multiplexing measurements across independent nanopore sensors in a format that can be scaled to enable high-throughput sequencing in future efforts. This system will be validated using protein standards and then applied to sequence and profile the kras protein-a key oncogenic driver of cancer progression-and its mutated forms, along with relevant ptms such as phosphorylation, glycosylation, and citrullination. Our goal is to demonstrate sequencing of cancer-relevant proteins with >98% accuracy. By enabling large-scale, high- throughput protein sequencing, this project will not only demonstrate its feasibility but also position IT as a powerful tool for accelerating the discovery of new cancer biomarkers and therapeutic targets. The advancement of oncoproteomics through this novel technology holds the potential to revolutionize cancer diagnostics and treatment, offering more precise tools for early detection, disease monitoring, and personalized therapies.
Quick answers
Who received award R21CA304932?
R21CA304932 was awarded to Electronic Biosciences, Inc. by National Cancer Institute (National Institutes of Health) on June 8, 2026.
How much is award R21CA304932 worth?
$418,854 has been obligated on R21CA304932.
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