2G3Z

Crystal structure of Transthyretin mutant I84A at low pH

Summary for 2G3Z

• Entry DOI: 10.2210/pdb2g3z/pdb
• Related: 1F41 2G3X 2G4E 2G4G
• Descriptor: Transthyretin (2 entities in total)
• Functional Keywords: ttr, amyloid fibrils formation, point mutation, transport protein
• Biological source: Homo sapiens (human)
• Cellular location: Secreted: P02766
• Total number of polymer chains: 2
• Total formula weight: 27470.56

Authors

Pasquato, N.,Folli, C.,Berni, R.,Zanotti, G. (deposition date: 2006-02-21, release date: 2007-01-16, Last modification date: 2023-10-25)

Primary citation

Pasquato, N.,Berni, R.,Folli, C.,Alfieri, B.,Cendron, L.,Zanotti, G.
Acidic pH-induced conformational changes in amyloidogenic mutant transthyretin.
J.Mol.Biol., 366:711-719, 2007

PubMed Abstract: Several proteins, including transthyretin (TTR), can generate in tissues extracellular insoluble aggregates, in the form of fibrils, that are associated with pathological states known as amyloidoses. To date, more than 80 different TTR point mutations have been associated with hereditary amyloidosis in humans. In vitro, the formation of amyloid fibrils by human TTR is known to be triggered by acidic pH. We show here that, in vitro, the natural amyloidogenic I84S and the non-natural I84A TTR mutant forms exhibit a propensity to produce fibrils in an acidic medium significantly higher than that of wild-type TTR. The two mutant forms have been crystallized at both neutral and acidic pH. Their neutral pH crystal structures are very similar to that of wild-type TTR, consistent with previous evidence indicating that only minor structural changes are induced by amyloidogenic mutations. On the contrary, their crystal structures at moderately low pH (4.6) show significant conformational differences as compared to their neutral pH structures. Remarkably, such changes are not induced in wild-type TTR crystallized at low pH. The most relevant consist of the unwinding of the TTR short alpha-helix and of the change in conformation of the loop connecting the alpha-helix to beta-strand F. Only one monomer of the crystallographic dimer is affected, causing a disruption of the tetrameric symmetry. This asymmetry and a possible destabilization of the tetrameric quaternary structure of TTR may be responsible for the amyloidogenic potential of the two TTR mutant forms at low pH.

PubMed: 17196219
DOI: 10.1016/j.jmb.2006.11.076

Experimental method

X-RAY DIFFRACTION (1.9 Å)