A Novel Millimeter-wave (mmw) DNP/EPR Front-end Compatible with Versatile High-field NMR Probes
Project Number1R43AG058519-01A1
Former Number1R43EB023736-01A1
Contact PI/Project LeaderDOTY, FRANCIS DAVID
Awardee OrganizationDOTY SCIENTIFIC, INC.
Description
Abstract Text
A Novel Millimeter-wave (mmw) DNP/EPR Front-end Compatible with Versatile High-field NMR Probes
Abstract
There has been explosive growth in interest in Dynamic Nuclear Polarization (DNP) with Magic Angle
Spinning (MAS) over the past five years because it has demonstrated S/N gains exceeding two orders of
magnitude at ~100 K compared to conventional MAS-NMR and non-spinning NMR of biological
macromolecules in their supramolecular assemblies under ambient conditions. The reduction in signal
acquisition time up to four orders is promising for a wide range of applications, and in particular structure
determination and function elucidation of biological macromolecules. Despite this enormous potential benefit,
the adaptation rate of DNP will be severely limited by its very high price tag (currently $2-6M), largely because
of the expensive gyrotron that has been required and because of the need for a special NMR magnet with
superconducting sweep coils (as the bandwidth of the gyrotron is very narrow).
Our preliminary simulations of a novel millimeter wave (mmw) DNP cavity that is compatible with a new
MAS spinner design have shown the potential for achieving the needed electron spin saturation with up to two
orders of magnitude lower microwave power than with existing MAS-DNP probes for samples of similar volume
(1-15 μL) and other conditions. With such an advance in mmw cavity design, along with the order-of-
magnitude progress in broad-band solid-state InP mmw power amplifiers seen over the past five years
(amplifiers now up to 850 GHz), it can become possible to eliminate both the gyrotron and need for a special
NMR magnet with superconducting sweep coils, even at NMR frequencies to 1200 MHz (800 GHz EPR).
These transformational advances can permit an enormous reduction in the cost of bringing MAS-DNP into an
ssNMR laboratory, thereby making it possible for virtually all current NMR groups to begin developing and
applying powerful new methods to structure determination and function elucidation of insoluble rigid proteins
and other macromolecules that are key to progress in developing cures for Alzheimer’s Disease and cancer.
However, in addition to the need for efficient MAS-DNP mmw spinner cavities, a novel low-cost EPR
mmw front-end (bridge) is critically needed so that EPR experiments can first be carried out within the high-
field NMR magnet on the prepared sample to facilitate essential calibration and optimization for the subsequent
MAS-DNP experiments. Unfortunately, the needed mmw front-end hardware is not available and a radically
new approach appears necessary if DNP is to become widely implemented.
This Phase-I would design, develop, and characterize a unique microelectronics mmw circuit for initial
demonstration (during the Phase-II) at 200GHz/300MHz that will be the basis for an add-on DNP/EPR front-
end accessory, eventually up to 800 GHz for existing high-field ssNMR spectrometers. Simulations, analysis,
and hardware tests will establish the potential for an order of magnitude reduction in system cost and two
orders of magnitude increase in EPR sensitivity compared to previously published approaches to high-field
EPR. Moreover, the novel approach will be compatible with H/X/Y MAS-DNP probes of commercially viable
designs.
Public Health Relevance Statement
A Novel Millimeter-wave (mmw) DNP/EPR Front-end Compatible with Versatile High-field NMR Probes
Narrative
Thousands of researchers are regularly using Nuclear Magnetic Resonance (NMR) techniques, with a
majority of the applications driven by the need for structure and function determination in biological
macromolecules. The advances developed under this project will allow almost every NMR laboratory to begin
applying Dynamic Nuclear Polarization (DNP) to both solids and liquids on a budget they will be able to afford,
equipping biomedical researchers with superb new tools for the structure-function studies of membrane
proteins, gaining information that is essential in developing cures for Alzheimer’s Disease and cancer.
NIH Spending Category
AgingBioengineering
Project Terms
Alzheimer's DiseaseAmplifiersAmyloid FibrilsBindingBiologicalBiomedical ResearchBudgetsCalibrationCommunicationComputer softwareDatabasesDepositionDetectionDevelopmentDevicesDropsElectronsEquipmentFrequenciesGrowthHIVLaboratoriesLiquid substanceMagicMalignant NeoplasmsMembrane ProteinsMethodsNMR SpectroscopyNuclearNuclear Magnetic ResonanceOpticsPharmaceutical PreparationsPhasePhysiologic pulsePlayPriceProteinsPublishingRaceRadarRattusReportingResearch PersonnelResolutionRoleSamplingScanning Tunneling MicroscopySideSignal TransductionSmall Business Innovation Research GrantSolidSourceStructureSystemTechniquesTestingTimeVertebral columnbasecostcryogenicsdesigndetectorexperimental studyfallsflexibilitygallium arsenideimprovedinstrumentinterestmacromoleculemicrowave electromagnetic radiationmillimeternanosecondnovelnovel strategiesprotein functionprototypesimulationsolid statesolid state nuclear magnetic resonancestructural biologytoolvirtual
No Sub Projects information available for 1R43AG058519-01A1
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 1R43AG058519-01A1
Patents
No Patents information available for 1R43AG058519-01A1
Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for 1R43AG058519-01A1
Clinical Studies
No Clinical Studies information available for 1R43AG058519-01A1
News and More
Related News Releases
No news release information available for 1R43AG058519-01A1
History
No Historical information available for 1R43AG058519-01A1
Similar Projects
No Similar Projects information available for 1R43AG058519-01A1