R01AT011990
Project Grant
Overview
Grant Description
Development and Validation of a High-Throughput MicroED-Driven Platform Technology for Natural Product Discovery - Abstract
This study is responsive to the Notice of Special Interest (NOSI) NOT-AT-21-006 "Fundamental Science Research on Complementary and Integrative Health Approaches, Including Natural Products or Mind and Body Interventions" objectives to "develop targeted and untargeted bioinformatic approaches to identify active components in a natural product mixture."
Structural elucidation of natural products (NPs) remains a critical rate-limiting step in NP discovery campaigns. Difficulties in structural elucidation can arise from i) the lack of sufficient quantities of material for traditional analytical methods (e.g. nuclear magnetic resonance (NMR) spectroscopy and X-ray crystallography); ii) intrinsic physical properties of the NP, and iii) limitations of NMR capabilities in determining relative configuration.
X-ray crystallography remains the gold-standard for unambiguous structural determination, including the assignment of stereochemistry. However, X-ray crystallographic analysis of newly-isolated NPs is often thwarted by insufficient quantities to provide crystals large enough for single-crystal diffraction or poor solid-state properties that preclude the formation of large, pristine crystals even when sufficient material is available.
Given these challenges, we envision that application of the recently reported cryo-electron microscopy (cryoEM) modality micro-crystal electron diffraction (MicroED) could lead to vertical advances in the field of NP discovery directly responsive to this NOSI, as MicroED has recently been demonstrated to provide unambiguous structures from sub-micron-sized crystals of structurally complex chemical compounds that had failed to yield large crystals suitable for X-ray analysis.
In this proposal, we aim to leverage a cryoEM/MicroED approach to resolving major bottlenecks in the structure elucidation of (partially) purified NPs and chemically complex NP mixtures. We hypothesize that we can advance the field of NP research through development and optimization of a high-throughput platform technology to identify NPs in complex mixtures and yield a novel diffractomics signature of molecules for integration into bioinformatics approaches.
To evaluate this hypothesis, we will carry out three specific aims:
1) Use MicroED to solve structures of recalcitrant (partially) purified NPs;
2) Develop a high-throughput MicroED-based platform for compound discovery; and
3) Resolve major bottlenecks in structure determination of complex NP mixtures.
For all aims, we will leverage a one-of-a-kind and expansive group of three NP collections (chemical libraries of extracts and partially purified fractions) derived from plants, marine organisms, and filamentous fungi. We anticipate advancement in the speed and accuracy of NP structural identification as a result of these studies, accelerating the rate of discovery of pharmacologically relevant NPs key to the improvement of human health.
This study is responsive to the Notice of Special Interest (NOSI) NOT-AT-21-006 "Fundamental Science Research on Complementary and Integrative Health Approaches, Including Natural Products or Mind and Body Interventions" objectives to "develop targeted and untargeted bioinformatic approaches to identify active components in a natural product mixture."
Structural elucidation of natural products (NPs) remains a critical rate-limiting step in NP discovery campaigns. Difficulties in structural elucidation can arise from i) the lack of sufficient quantities of material for traditional analytical methods (e.g. nuclear magnetic resonance (NMR) spectroscopy and X-ray crystallography); ii) intrinsic physical properties of the NP, and iii) limitations of NMR capabilities in determining relative configuration.
X-ray crystallography remains the gold-standard for unambiguous structural determination, including the assignment of stereochemistry. However, X-ray crystallographic analysis of newly-isolated NPs is often thwarted by insufficient quantities to provide crystals large enough for single-crystal diffraction or poor solid-state properties that preclude the formation of large, pristine crystals even when sufficient material is available.
Given these challenges, we envision that application of the recently reported cryo-electron microscopy (cryoEM) modality micro-crystal electron diffraction (MicroED) could lead to vertical advances in the field of NP discovery directly responsive to this NOSI, as MicroED has recently been demonstrated to provide unambiguous structures from sub-micron-sized crystals of structurally complex chemical compounds that had failed to yield large crystals suitable for X-ray analysis.
In this proposal, we aim to leverage a cryoEM/MicroED approach to resolving major bottlenecks in the structure elucidation of (partially) purified NPs and chemically complex NP mixtures. We hypothesize that we can advance the field of NP research through development and optimization of a high-throughput platform technology to identify NPs in complex mixtures and yield a novel diffractomics signature of molecules for integration into bioinformatics approaches.
To evaluate this hypothesis, we will carry out three specific aims:
1) Use MicroED to solve structures of recalcitrant (partially) purified NPs;
2) Develop a high-throughput MicroED-based platform for compound discovery; and
3) Resolve major bottlenecks in structure determination of complex NP mixtures.
For all aims, we will leverage a one-of-a-kind and expansive group of three NP collections (chemical libraries of extracts and partially purified fractions) derived from plants, marine organisms, and filamentous fungi. We anticipate advancement in the speed and accuracy of NP structural identification as a result of these studies, accelerating the rate of discovery of pharmacologically relevant NPs key to the improvement of human health.
Awardee
Funding Goals
NOT APPLICABLE
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Atlanta,
Georgia
303224250
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 1788% from $170,717 to $3,222,429.
Emory University was awarded
High-Throughput MicroED Platform for Natural Product Discovery
Project Grant R01AT011990
worth $3,222,429
from National Center for Complementary and Integrative Health in May 2022 with work to be completed primarily in Atlanta Georgia United States.
The grant
has a duration of 4 years 9 months and
was awarded through assistance program 93.310 Trans-NIH Research Support.
The Project Grant was awarded through grant opportunity NIH Research Project Grant (Parent R01 Clinical Trial Not Allowed).
Status
(Ongoing)
Last Modified 5/21/26
Period of Performance
5/6/22
Start Date
2/28/27
End Date
Funding Split
$3.2M
Federal Obligation
$0.0
Non-Federal Obligation
$3.2M
Total Obligated
Activity Timeline
Subgrant Awards
Disclosed subgrants for R01AT011990
Transaction History
Modifications to R01AT011990
Additional Detail
Award ID FAIN
R01AT011990
SAI Number
R01AT011990-3146423494
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Private Institution Of Higher Education
Awarding Office
75NY00 NIH National Center for Complementary & Integrative Health
Funding Office
75NY00 NIH National Center for Complementary & Integrative Health
Awardee UEI
S352L5PJLMP8
Awardee CAGE
2K291
Performance District
GA-05
Senators
Jon Ossoff
Raphael Warnock
Raphael Warnock
Budget Funding
| Federal Account | Budget Subfunction | Object Class | Total | Percentage |
|---|---|---|---|---|
| National Center for Complementary and Integrative Health, National Institute of Health, Health and Human Services (075-0896) | Health research and training | Grants, subsidies, and contributions (41.0) | $982,643 | 75% |
| Office of the Director, National Institutes of Health, Health and Human Services (075-0846) | Health research and training | Grants, subsidies, and contributions (41.0) | $332,303 | 25% |
Modified: 5/21/26