How the key proteins behind autosomal dominant polycystic kidney disease work

Structural Mechanisms of Polycystic Kidney Disease Proteins

NIH-funded research Utah State Higher Education System--University of Utah · NIH-11321734

This project looks at the shapes and assembly of the proteins that cause autosomal dominant polycystic kidney disease to help people with ADPKD.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUtah State Higher Education System--University of Utah NIH-funded
Lab location1 site (Salt Lake City, United States)
Project IDNIH-11321734 on NIH RePORTER

What this research studies

I would describe this as lab research that aims to reveal the three-dimensional shapes and how PKD1, PKD2, and related polycystin proteins fit together in tiny cell structures called primary cilia. The team uses biochemical assays, structural imaging, and model systems to see how mutations change protein assembly and channel function. They also study related family members (like PKD1L1 and PKD2L2) that affect development and reproduction to broaden the picture. The work connects genetic changes found in people with ADPKD to specific molecular problems in the proteins.

Who could benefit from this research

Good fit: People with autosomal dominant polycystic kidney disease or a strong family history of ADPKD are the population most directly related to this research.

Not a fit: Patients whose kidney disease is caused by non-PKD genes or by unrelated conditions are unlikely to see direct benefit from these findings in the near term.

Why it matters

Potential benefit: If successful, this work could point to new drug targets or biomarkers that might slow cyst growth or guide personalized treatments for ADPKD patients.

How similar studies have performed: Previous genetic and functional studies have linked PKD1 and PKD2 to ADPKD, but high-resolution structures and detailed assembly mechanisms remain largely uncharacterized.

Where this research is happening

Salt Lake City, 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 Adult Polycystic Kidney DiseaseAutosomal Dominant Polycystic Kidney Disease
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.