PIPages
Labs

Stefan Oliver

Stanford University, CA·Biophysics

Herpesviruses enter cells using proteins studded in their outer membrane, and those same proteins are what the immune system learns to recognize. Varicella-zoster virus, the agent of chickenpox and shingles, is a case in point: it can cause severe disease in people with weakened immune systems, lead to long-lasting nerve pain known as post-herpetic neuralgia, and has been linked to stroke.

Fields

Biophysics

Microbiology & Immunology

Biochemistry

Topics

varicella-zoster virus

herpesvirus

cryo-electron microscopy

Grants
1 known grant, through Jan 2028

What they work on

  1. Determine the near-atomic structure of the varicella-zoster virus gB/gH-gL complex, the machinery that fuses viral and cell membranes, using single-particle cryo-electron microscopy on complexes kept in their native lipid environment.
  2. Relate the shape of the gB/gH-gL complex to its fusion function, to explain mechanistically how herpesviruses merge with the cells they infect.
  3. Solve the structure of the gE/gI glycoprotein pair, which supports viral replication and spread, both on its own and in complex with antibodies that recognize it.
  4. Use CyclApol-based membrane extraction to purify intact glycoprotein complexes from virus-infected cells, avoiding detergents that strip away surrounding lipids.

More about the research

Yet the shapes of its entry proteins, and how they move to pull two membranes together, are largely unknown. This work uses structural imaging to see those machines as they actually sit in a membrane.

Why it matters

Chickenpox and shingles remain common, and their complications include chronic nerve pain and increased stroke risk. Detailed structures of the viral proteins that drive cell entry and antibody recognition could give vaccine designers and antiviral developers concrete targets to aim at, and because herpesviruses share this fusion machinery, the findings may inform work on related viruses.

Known grants

From NIH and NSF research grants. Labs often have other funding we can't see.

Cryo-EM structures of herpesvirus glycoprotein complexes in native membranes: insights into viral entry and immunity

NIH · Feb 2026 – Jan 2028

Closest labs

David Koelle

University of Washington, WA·Microbiology & Immunology

Expand the collection of varicella zoster virus-specific human monoclonal antibodies cloned from shingles skin biopsies and map their fine specificity against viral envelope, tegument, enzyme, and nuclear proteins.

Kai Xu

Ohio State University, OH·Biophysics

Determine structures of soluble, stabilized G and F glycoprotein ectodomains from emerging henipaviruses, including the bat-borne Cedar virus and Angavokely virus, to capture the full tetrameric G and the fragile prefusion F.

James Lee

New York University, NY·Microbiology & Immunology·Early-career

Map the complete route of peptide antigen loading onto MHC-I molecules using a chemical biology strategy applied both in living cells and in reconstituted systems rebuilt from purified components.

The school

Stanford University: 87 labs on PI Pages, $1.6B a year on research, 739 research doctorates a year.

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