David S. Eisenberg
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Recognitions
David S. Eisenberg has a total of 661 co-authors. Here are the top co-authors by number of shared publications:
- Michael R. Sawaya
Department of Chemistry and Biochemistry, University of California, Los Angeles
77 shared publications Duilio Cascio
39 shared publicationsMichael R. Sawaya
26 shared publications- David R. Boyer
University of California Los Angeles
23 shared publications David R. Boyer
14 shared publicationsRomany Abskharon
14 shared publications
Latest Publications
- Open Access
- 8 September 2026
- Published by National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 123 (37)
Cryo-EM structure of TGFBIp fibrils driven by a corneal dystrophy–linked mutation enables design of peptide inhibitors of aggregation
Corneal dystrophy is a heterogeneous group of diseases which manifests clinically by progressive corneal opacity and diminishing visual acuity. A group of corneal dystrophies are linked to autosomal dominant mutations in transforming growth factor β–induced protein (TGFBIp) and characterized by extracellular amyloid-positive deposits of unknown molecular structure. Here, we determined the cryogenic-electron microscopy (cryo-EM) structure of amyloid fibrils formed by the TGFBIp FAS1-4 domain with corneal dystrophy–linked mutation V624M. The L569 to N609 fibril core, which includes the Y571-R588 segment enriched in patient corneal deposits, forms symmetrical protofilaments with internal solvent channels. Leveraging this structure, we designed peptide inhibitors intended to bind onto fibril ends to block elongation, targeting the unequal growth of symmetrical protofilaments. Our G1 and H4 inhibitors exhibit concentration-dependent reduction of TGFBIp FAS1-4 aggregation as assessed by Thioflavin T, solubility fractionation, and electron microscopy. Our work illustrates how fibril structures can guide rational inhibitor design and suggests the targeting of protein aggregates as a therapeutic approach for corneal and ocular diseases.
- 8 September 2026
- Published by National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 123 (37)
Open AccessCryo-EM structure of TGFBIp fibrils driven by a corneal dystrophy–linked mutation enables design of peptide inhibitors of aggregation
Corneal dystrophy is a heterogeneous group of diseases which manifests clinically by progressive corneal opacity and diminishing visual acuity. A group of corneal dystrophies are linked to autosomal dominant mutations in transforming growth factor β–induced protein (TGFBIp) and characterized by extracellular amyloid-positive deposits of unknown molecular structure. Here, we determined the cryogenic-electron microscopy (cryo-EM) structure of amyloid fibrils formed by the TGFBIp FAS1-4 domain with corneal dystrophy–linked mutation V624M. The L569 to N609 fibril core, which includes the Y571-R588 segment enriched in patient corneal deposits, forms symmetrical protofilaments with internal solvent channels. Leveraging this structure, we designed peptide inhibitors intended to bind onto fibril ends to block elongation, targeting the unequal growth of symmetrical protofilaments. Our G1 and H4 inhibitors exhibit concentration-dependent reduction of TGFBIp FAS1-4 aggregation as assessed by Thioflavin T, solubility fractionation, and electron microscopy. Our work illustrates how fibril structures can guide rational inhibitor design and suggests the targeting of protein aggregates as a therapeutic approach for corneal and ocular diseases.
- Open Access
- 16 April 2026
- Published by EMBL-EBI
Filament of D-TLKIVWR, a D-peptide that disaggregates Alzheimer's Paired Helical Filaments
EMPIAR, the Electron Microscopy Public Image Archive centered at EMBL-EBI, is a public resource for raw electron microscopy images related to EMDB, contains micrographs, particle sets and tilt-series.
- 16 April 2026
- Published by EMBL-EBI
Open AccessFilament of D-TLKIVWR, a D-peptide that disaggregates Alzheimer's Paired Helical Filaments
EMPIAR, the Electron Microscopy Public Image Archive centered at EMBL-EBI, is a public resource for raw electron microscopy images related to EMDB, contains micrographs, particle sets and tilt-series.
- Open Access
- 16 April 2026
- Published by EMBL-EBI
Filament of D-TLKIVWI, a D-peptide that disaggregates Alzheimer's Paired Helical Filaments
EMPIAR, the Electron Microscopy Public Image Archive centered at EMBL-EBI, is a public resource for raw electron microscopy images related to EMDB, contains micrographs, particle sets and tilt-series.
- 16 April 2026
- Published by EMBL-EBI
Open AccessFilament of D-TLKIVWI, a D-peptide that disaggregates Alzheimer's Paired Helical Filaments
EMPIAR, the Electron Microscopy Public Image Archive centered at EMBL-EBI, is a public resource for raw electron microscopy images related to EMDB, contains micrographs, particle sets and tilt-series.
- Open Access
- 16 April 2026
- Published by EMBL-EBI
Filament of D-TLKIVWS, a D-peptide that disaggregates Alzheimer's Paired Helical Filaments
- 16 April 2026
- Published by EMBL-EBI
Open AccessFilament of D-TLKIVWS, a D-peptide that disaggregates Alzheimer's Paired Helical Filaments
- Open Access
- 16 April 2026
- Published by EMBL-EBI
Tau Paired Helical Filament from Alzheimer's Disease before addition of D-peptide disaggregants
- 16 April 2026
- Published by EMBL-EBI
Open AccessTau Paired Helical Filament from Alzheimer's Disease before addition of D-peptide disaggregants
- Open Access
- 14 April 2026
- Published by EMBL-EBI
Tau Paired Helical Filament from Alzheimer's Disease incubated with D-peptide D-TLKIVWS
EMPIAR, the Electron Microscopy Public Image Archive centered at EMBL-EBI, is a public resource for raw electron microscopy images related to EMDB, contains micrographs, particle sets and tilt-series.
- 14 April 2026
- Published by EMBL-EBI
Open AccessTau Paired Helical Filament from Alzheimer's Disease incubated with D-peptide D-TLKIVWS
EMPIAR, the Electron Microscopy Public Image Archive centered at EMBL-EBI, is a public resource for raw electron microscopy images related to EMDB, contains micrographs, particle sets and tilt-series.
- Open Access
- 14 April 2026
- Published by EMBL-EBI
Tau Paired Helical Filament from Alzheimer's Disease incubated with D-peptide D-TLKIVWR
EMPIAR, the Electron Microscopy Public Image Archive centered at EMBL-EBI, is a public resource for raw electron microscopy images related to EMDB, contains micrographs, particle sets and tilt-series.
- 14 April 2026
- Published by EMBL-EBI
Open AccessTau Paired Helical Filament from Alzheimer's Disease incubated with D-peptide D-TLKIVWR
EMPIAR, the Electron Microscopy Public Image Archive centered at EMBL-EBI, is a public resource for raw electron microscopy images related to EMDB, contains micrographs, particle sets and tilt-series.
- Open Access
- 13 April 2026
- Published by EMBL-EBI
Tau Paired Helical Filament from Alzheimer's Disease incubated with D-peptide D-TLKIVWI
EMPIAR, the Electron Microscopy Public Image Archive centered at EMBL-EBI, is a public resource for raw electron microscopy images related to EMDB, contains micrographs, particle sets and tilt-series.
- 13 April 2026
- Published by EMBL-EBI
Open AccessTau Paired Helical Filament from Alzheimer's Disease incubated with D-peptide D-TLKIVWI
EMPIAR, the Electron Microscopy Public Image Archive centered at EMBL-EBI, is a public resource for raw electron microscopy images related to EMDB, contains micrographs, particle sets and tilt-series.