SBIR/STTR Research Award

Novel Materials and Methods for Separations of Glycopeptides and Glycans

Award identifier 71026599e10ca972ec01a024e1c9ca101f6bf26592042dd89008bfb5fa1f40efAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$1,161,877

Program and phase

SBIR · Phase II

Award year

2013

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
ADVANCED MATERIALS TECHNOLOGY, INC.
Proposal award date
2013-08-01
Contract end date
2016-11-30
UEI
FYGPW6JX4L98
Solicitation number
PA11-215
Topic code
NIGMS

Research abstract

DESCRIPTION provided by applicant Analysis of glycoprotein polypeptide sites of carbohydrate attachment and the structures of the glycans present on these proteins requires the combination of high resolution chromatographic separations and sophisticated mass spectrometry Hydrophilic interaction liquid chromatography HILIC has great use in separations of glycopeptides and released glycans exhibiting remarkable selectivity for the separations of glycoforms The proposed effort is to markedly improve separations of glycopeptides and released glycans by HILIC reducing the separation times from the current hours per sample to minutes or less The separations component of LC MS analysis of glycoproteins can benefit from the design of more efficient stationary phase chromatographic materials and from the use of conditions that allow direct and productive interfacing with mass spectrometers We propose that recently developed superficially porous silica microparticulate silica packing materials Fused Core R structures can achieve these separation speeds without loss of the required high resolution The AMT Fused Core reversed phase materials have previously been shown to exhibit superior kinetic properties and column efficiencies for separations of small molecules and recently wider pore size packings have shown a similar benefit for larger peptides c kDa The current proposal uses Fused Core technology with unique surface modifications to develop high performance HILIC materials specifically for separations of glycopeptides and glycans Tailored HILIC materials will be synthesized and tested for HILIC operation as well as to establish the fundamental relationships between surface properties particle characteristics and utility for glycan and glycopeptides separations The new bonded phases utilize organosilane chemistry discovered in Phase I efforts that have been selected to withstand aggressive conditions of use permitting stable and robust separations materials that can be used across a broad range of conditions Preliminary LC MS applications in glycoproteomic applications have been completed in Phase A reasonable estimate is that an improvement of andgt fold for separations times are obtained Phase II will expand on this effort with the purpose of delivering further improved materials and methods to a broader range of needs in glycoproteomics and proteomics workflows A significant aspect of the current proposal will assess the benefits and real world applications of these new separations materials The target of this work is to produce robust materials that permit simple integration with online mass spectrometry analysis effective for resolution of the complex mixtures that are typical of current glycoprotein identification and structural characterization procedures PUBLIC HEALTH RELEVANCE Protein modification by the addition of sugars called glycosylation is extremely common in nature and this modification exhibits a strong effect on protein structure and on biological function In certain diseases most notably in cancer and for some infectious diseases like influenza glycosylation of proteins or recognition of such proteins is altered in ways that are not fully understood In some cases these alterations are big enough to allow them to be used for recognition of disease and in some cases to stratify patients The current proposal is to use new knowledge in materials science and chemistry to enable much faster and more efficient ways to discover glycosylation disease markers and to better understand the biology of glycosylation

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

21 SBIR/STTR records share this UEI (2004–2021). Reported award amounts total $8,851,639. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services, National Aeronautics and Space Administration, Department of Defense

Agency intelligence

Department of Health and Human Services

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