PROJECT SUMMARY: Fannin Innovation Studio is developing a new discovery proteomics platform called the
Unified Process that identifies potential biomarkers in biological samples and simultaneously selects their affinity
reagents (Raptamers). Currently, the translation of biomarkers from discovery to clinical utilization has been low;
to address this problem, the Unified Process seeks to commercialize a rapid, high-throughput platform that
establishes a powerful linkage between mass-spectrometry-based and affinity-based approaches to allow for
early assay development for use in the validation of the identified potential biomarkers.
A key component of the Unified Process utilizes Raptamer combinatorial library beads, which are next-
generation oligonucleotides with several chemical modifications attached to the DNA bases and/or in the
backbone. The major steps to the Unified Process include: 1) Raptamer library beads are incubated with samples
specific to a disease phenotype and control samples, followed by sorting by flow cytometry, with each sorted
bead having unique Raptamer sequences that will be bound to the yet unidentified protein; 2) Raptamer
oligonucleotides are released from the sorted beads and pulled down with biotinylated biofluid in a multiplexed
step; 3) Raptamer oligonucleotides are identified by sequencing and are synthesized and used to pull down
biomarker candidates from the biological samples; and 4) LC/MS/MS identifies the biomarker candidates.
Notably, the resulting Raptamers are immediately available for downstream applications to precisely quantify the
identified potential biomarkers in formats such as enzyme-linked oligonucleotide assays (ELONAs) and selected
reaction monitoring (SRM) MS. The availability of Raptamer affinity reagents to potential biomarkers so early in
the discovery phase will accelerate the verification and subsequent validation of candidates, saving significant
time and expense translating discoveries into the clinic.
This proposed project is focused integrating, optimizing, and fully characterizing this novel approach for
successful implementation of the Unified Process. The Phase I aim are: Aim 1: Optimize the Unified Process
to decrease the lead time in identification of proteins. The goal is to decrease the lead time of this process
by at least 25% with a goal of 50% by successfully moving directly from bead sorting to mass spectrometry. Aim
2: Demonstrate retrieval of known biomarkers from various sample types using the optimized Unified
Process. The goals are to determine the limit of detection of the potential protein biomarkers in various tissue
types and to identify potential Raptamers that can be new affinity reagents for these existing biomarkers.
Successful completion of this study will demonstrate proof of concept for the Unified Process and will position
us for an SBIR Phase II project to characterize unknown biomarkers in various disease types. Ultimately, Fannin
Innovation Studio plans to commercialize the Unified Process by selling it as a service and retaining the rights
to commercialize the resulting Raptamers for use in potential research and clinical diagnostic assays.