Program of Biophysics · University of Michigan

Magdalena Ivanova, PhD

Protein folding, phase separation, and aggregation in neurodegenerative disease.

Affiliations in the Neuroscience Graduate Program and the Michigan Neuroscience Institute.

About

Our research examines protein folding, liquid–liquid phase separation, and aggregation, and how these processes contribute to disease. We study the misfolding, toxic species formation, and abnormal assembly of proteins including α-synuclein, amyloid-β, tau, TDP-43, and UBQLN2, whose pathogenic accumulation underlies a group of devastating and often terminal disorders known as proteinopathies. Combining biophysics, computational modeling, biochemistry, and cell biology, we work to define the mechanisms driving protein misfolding and to translate that understanding into therapeutic strategies.

Research

Two questions at the center of our work.

Our projects connect molecular self-assembly with protein quality control, disease-specific structures, propagation, and cellular outcomes.

01

Brain-expressed ubiquilins in normal function and disease

The brain-expressed ubiquilins (UBQLN1, 2, and 4) maintain protein homeostasis by clearing damaged and misfolded proteins; mutations in UBQLN2 and UBQLN4 drive pathogenic aggregation in familial ALS/FTD, and ubiquilin dysfunction has been linked to Huntington's disease and the synucleinopathies. Liquid–liquid phase separation appears central to how they work — concentrating them where needed, but also tipping them toward pathological aggregation. We ask what governs that balance at the molecular level, in health and in disease.

ProteostasisPhase separationALS / FTD
02

Molecular studies of α-synuclein aggregation

One protein, several diseases. α-Synuclein aggregates in Parkinson's disease, dementia with Lewy bodies, Alzheimer's disease with Lewy bodies, and multiple system atrophy — yet these disorders differ markedly in pathology and clinical course. We think the answer lies in structure: using computational, biophysical, and cellular approaches, we characterize the structural heterogeneity of α-synuclein inclusions across these diseases and ask how distinct assemblies give rise to distinct phenotypes and how they propagate.

Structural heterogeneityPropagationSynucleinopathies
Teaching

Physics and chemistry as tools for understanding life.

Courses connect foundational principles with biological systems, biomedical applications, quantitative analysis, landmark discoveries, and modern biophysical tools.

Fall 2026

Biophysics of Life

BIOPHYS 120
Winter 2026

Biocomplexity

BIOPHYS 433 · PHYSICS 433
Winter 2026

Medical Physics

BIOPHYS 430 · PHYSICS 430
Teaching history
  • Biophysics of Life / Discovery of the DNA Double Helix — since Fall 2025
  • Physical and Chemical Principles Behind Biology and Medicine — since Fall 2024
  • Medical Physics — since Winter 2020
  • Biocomplexity — since Winter 2025
  • Biophysics of Disease — Fall 2014–Fall 2024

Course listings are available through the Biophysics undergraduate courses page. Interested students are welcome to get in touch.

Editorial & Service
Publications

Recent work, 2020–2026.

Browse peer-reviewed research spanning amyloid oligomers, membrane interactions, ubiquilins, α-synuclein, C9orf72, NOTCH3, and protein quality control.

Selected · since 2020

Scholarly record
7,137Citations
29h-index
39i10-index

Citation metrics via Google Scholar · Updated August 2026.

Contact
Magdalena I. Ivanova, PhD Program of Biophysics
930 N. University Ave.
University of Michigan
Ann Arbor, MI 48109
Phone 734 647 9869
Email [email protected]