How certain cell transport proteins move fatty acids into peroxisomes

Molecular basis of fatty acid transport by peroxisomal ABC transporters

NIH-funded research University of Minnesota · NIH-11146365

Researchers will use biochemical and high-resolution imaging tools to learn how ABCD transport proteins move very-long-chain fatty acids, aiming to better understand disorders like X‑linked adrenoleukodystrophy.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniversity of Minnesota NIH-funded
Lab location1 site (Minneapolis, United States)
Project IDNIH-11146365 on NIH RePORTER

What this research studies

This project uses purified proteins, lab-grown cells, and patient-derived mutations to watch how ABCD transporters pick up and move very-long-chain and branched fatty acids into peroxisomes. Scientists will combine biochemical tests, cell biology experiments, cryo-electron microscopy, and EPR spectroscopy to see transporter shapes and motions during transport. They will compare normal ABCD1 with disease-causing ABCD1 variants and with related ABCD2 and ABCD3 proteins to find what goes wrong in disease. The work focuses on molecular details that could explain lipid buildup and nerve damage seen in peroxisomal disorders.

Who could benefit from this research

Good fit: People with X‑linked adrenoleukodystrophy or other peroxisomal fatty acid metabolism disorders, and individuals known to carry ABCD1/ABCD2/ABCD3 mutations, would be the most relevant candidates.

Not a fit: Patients with neurological or metabolic conditions unrelated to peroxisomal fatty acid transport are unlikely to receive direct benefit from this work.

Why it matters

Potential benefit: If successful, the findings could point to new targets for treatments or diagnostics for X‑linked adrenoleukodystrophy and related peroxisomal lipid disorders.

How similar studies have performed: Related structural and biochemical work on other ABC transporters has yielded useful insights, but applying cryo-EM and EPR specifically to ABCD transporters and disease variants is relatively new.

Where this research is happening

Minneapolis, United States

Researchers

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page below.
Conditions Addison disease-cerebral sclerosis syndromeAddison disease-spastic paraplegia syndromeAddison-Schilder syndrome
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.