SBIR/STTR Research Award

Directed evolution of N terminal amino acid binding proteins for application to protein sequencing

Award identifier 863c2b01bed209422f91cedd0973a4a75071f81004199ab9cd8957075433b31bAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$223,600

Program and phase

SBIR · Phase I

Award year

2017

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
ENCODIA INC
Proposal award date
2017-09-01
Contract end date
2018-08-31
UEI
XQMHALBLACC9
Solicitation number
PA16-302
Topic code
300

Research abstract

ABSTRACT including UNDERLYING PREMISE and STRATEGY to ENSURE ROBUSTNESS Our premise is that developing a better method for analyzing proteomes is required to take full advantage of the technological breakthroughs that have occurred in the last years in DNA sequencing We believe that the difficulties associated with previous proteome analysis methods can be overcome by using an entirely different approach We propose to test this premise by obtaining affinity reagents to N terminal amino acids that can be used in a new massively parallel method for protein sequencing Our strategy to ensure a robust unbiased and reduced risk approach is to develop in parallel the directed evolution of two protein scaffolds and compare them to commercially available and naturally occurring IgG affinity reagents We have chosen methods that are extremely well established in our lab phage display screening in both bulk and emulsions phage display library construction and affinity maturation The two scaffolds for display include lipocalins and scFv Abs While not discussed in the proposal if there is time remaining or if a specific need arises we may try other scaffolds NARRATIVE and OVERALL IMPACT The overall impact of RNA sequencing and digital counting is significant in biological research But RNA molecule counting can only be used as a surrogate for protein abundance That results in a couple of outstanding problems In many cases there appears to be a limited correlation for RNA levels and protein abundance And RNA abundance gives absolutely no information with regard to post translational modification of proteins that is so important to cell signaling and other biological processes We believe the proposed development of a ProCode system will significantly impact many areas of science just as NextGen sequencing has done for genome analysis There are several components to the proposed system development of the assay including proprietary reagents the focus of this proposal instrumentation and software which includes instrumentation control and bioinformatics This proposal will focus on component the development of the binding reagents needed for the ProCode assay Specifically we will describe the experiments needed to generate the N terminal amino acid NTAA recognizing affinity reagents for use in the ProCode assay

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

8 SBIR/STTR records share this UEI (2016–2021). Reported award amounts total $6,255,660. Reported amounts are not federal obligations.

Phases: Phase I, Phase II, Phase II – Direct to Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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