9D27

Cryo-EM structure of amyloid fibril extracted from kidney of a variant ATTR T60A amyloidosis patient 3

Summary for 9D27

• Entry DOI: 10.2210/pdb9d27/pdb
• Related: 9D21 9D23 9D24
• EMDB information: 46479 46481 46482 46487
• Descriptor: Transthyretin (1 entity in total)
• Functional Keywords: transthyretin, amyloidosis, attr, kidney, protein fibril
• Biological source: Homo sapiens (human)
• Total number of polymer chains: 5
• Total formula weight: 68736.67

Authors

Nguyen, A.B.,Fernandez-Ramirez, M.C.,Saelices, L. (deposition date: 2024-08-08, release date: 2025-08-13, Last modification date: 2025-10-29)

Primary citation

Fernandez-Ramirez, M.D.C.,Nguyen, B.A.,Afrin, S.,Singh, V.,Evers, B.,Shelton, J.M.,Escobar, C.L.,Bassett, P.,Wang, L.,Pekala, M.,Ahmed, Y.,Cabrera Hernandez, L.O.,Pedretti, R.,Singh, P.,Canepa, J.,Wosztyl, A.,Li, Y.,Boyer, D.R.,Cao, Q.,Saelices, L.
Structural and molecular homogeneity of ATTRv-T60A amyloid fibrils across patients and organs.
Structure, 2025

PubMed Abstract: Transthyretin amyloidosis is a systemic protein misfolding disorder with diverse clinical phenotypes, including cardiomyopathy, polyneuropathy, or a combination of both. While structural polymorphism of amyloid fibrils has been linked to disease heterogeneity in neurodegenerative disorders, its role in transthyretin amyloidosis remains unclear. Here, we used cryo-electron microscopy to analyze ex vivo fibrils extracted from the hearts of three patients carrying the T60A mutation, a variant associated with mixed cardiac and neuropathic symptoms. In one patient, we additionally examined fibrils from the thyroid, kidney, and liver. All fibrils across patients and tissues adopted a single morphology previously associated with cardiomyopathy. Complementary molecular analyses revealed high compositional homogeneity. Notably, we extracted fibrils from the liver, an organ considered fibril-free, with seeding capacity in vitro. These findings suggest structural homogeneity as a hallmark of cardiac and mixed phenotypes, and provide a mechanistic rationale for the transmission of amyloidosis following domino liver transplantation.

PubMed: 41106377
DOI: 10.1016/j.str.2025.09.008

Experimental method

ELECTRON MICROSCOPY (3.19 Å)