# Identification of essential sites of lipid peroxidation in ferroptosis using Raman spectroscopy imaging

> **NIH NIH F30** · COLUMBIA UNIVERSITY HEALTH SCIENCES · 2020 · $45,525

## Abstract

Project Summary
Ferroptosis, an iron-dependent form of non-apoptotic regulated cell death, has been suggested as a cause of
neuronal death in neurodegenerative disorders such as Alzheimer’s disease. Ferroptotic death is due to an
uncontrolled iron-mediated accumulation of phospholipid hydroperoxides. Iron and lipid-based reactive oxygen
species are both increased in the brains of patients with Alzheimer’s disease, and induction of ferroptosis in the
forebrain neurons of mice by knocking out GPX4, an anti-ferroptotic peroxidase, results in Alzheimer-like
symptoms. Anti-oxidants such as vitamin E and iron chelators have been moderately effective in Alzheimer’s
disease patients, and we attribute their limited efficacy to low potency and improper biodistribution. Our goal is
to define precisely where lipid peroxides need to form to drive the cell death characteristic of ferroptosis, and
ultimately whether this process contributes to Alzheimer’s disease. In this study, a group of mechanistically
distinct ferroptosis inhibitors will be localized in cells using stimulated Raman spectroscopy (SRS) imaging.
SRS imaging allows sensitive detection of compound distribution in live cells without bulky fluorescent tags;
compounds are instead labeled with small, aliphatic probes containing Raman-active functional groups such as
diynes. The distribution of these ferroptosis inhibitors will illuminate candidate subcellular sites that require
protection to inhibit ferroptosis. By comparing the distributions of these compounds, we can hypothesize which
organelles/membranes are key sites of lipid peroxidation in ferroptotic death. We will then investigate these
organelles/membranes by specifically modulating their sensitivity to ferroptotic lipid peroxidation, in order to
determine their contribution to ferroptosis. This will be accomplished by targeting established pro- and anti-
ferroptotic proteins to these subcellular sites, and evaluating changes in sensitivity to ferroptosis inducers.
Through this systematic approach, we will identify whether one or more subcellular components are essential
to ferroptotic death. In summary, the aims of this project are to (i) to determine the subcellular localization of
ferroptosis inhibitors to identify targets of drugs inhibiting neurodegenerative oxidative cell death, and (ii) to
identify the essential membranes for inhibition and induction of ferroptotic death in neurons through targeted
modulation of sensitivity to ferroptotic lipid peroxidation. The results of this project will deepen our
understanding of this pathological cell death pathway, as well as enhance future development of ferroptosis-
inhibiting compounds that could become disease-modifying treatments for Alzheimer’s and other
neurodegenerative diseases. Through this project, the trainee will advance his biological and chemical
laboratory skills with novel techniques, develop a strong research acumen, and gain scientific writing and
presentation experience, al...

## Key facts

- **NIH application ID:** 10067795
- **Project number:** 1F30AG066272-01A1
- **Recipient organization:** COLUMBIA UNIVERSITY HEALTH SCIENCES
- **Principal Investigator:** Alfred Nikolai von Krusenstiern
- **Activity code:** F30 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $45,525
- **Award type:** 1
- **Project period:** 2020-09-01 → 2023-08-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10067795

## Citation

> US National Institutes of Health, RePORTER application 10067795, Identification of essential sites of lipid peroxidation in ferroptosis using Raman spectroscopy imaging (1F30AG066272-01A1). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/10067795. Licensed CC0.

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