4.0-Å resolution cryo-EM structure of the mammalian chaperonin TRiC/CCT reveals its unique subunit arrangement

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 107; no. 11; pp. 4967 - 4972
• Main Authors: Cong, Yao, Baker, Matthew L, Jakana, Joanita, Woolford, David, Miller, Erik J, Reissmann, Stefanie, Kumar, Ramya N, Redding-Johanson, Alyssa M, Batth, Tanveer S, Mukhopadhyay, Aindrila, Ludtke, Steven J, Frydman, Judith, Chiu, Wah
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 16.03.2010; National Acad Sciences
• Subjects: Aggregation; Amino Acid Sequence; Animals; Biochemistry; Biological Sciences; Cattle; Cells; Chaperonin Containing TCP-1 - chemistry; Chaperonins; Chemical properties; Cryoelectron Microscopy; Crystal structure; Crystallography, X-Ray; Disease models; Mammals; Models, Molecular; Molecular Sequence Data; Molecular structure; physicochemical properties; Prokaryotes; prokaryotic cells; Protein folding; Protein Structure, Secondary; Protein Subunits - chemistry; proteome; Proteomics; Reproducibility of Results; sequence homology; Static Electricity; substrate specificity; Surface Properties; Symmetry; Ungulates
• ISSN: 0027-8424; 1091-6490; 1091-6490
• DOI: 10.1073/pnas.0913774107

The essential double-ring eukaryotic chaperonin TRiC/CCT (TCP1-ring complex or chaperonin containing TCP1) assists the folding of ~5-10% of the cellular proteome. Many TRiC substrates cannot be folded by other chaperonins from prokaryotes or archaea. These unique folding properties are likely linked to TRiC's unique heterooligomeric subunit organization, whereby each ring consists of eight different paralogous subunits in an arrangement that remains uncertain. Using single particle cryo-EM without imposing symmetry, we determined the mammalian TRiC structure at 4.7-Å resolution. This revealed the existence of a 2-fold axis between its two rings resulting in two homotypic subunit interactions across the rings. A subsequent 2-fold symmetrized map yielded a 4.0-Å resolution structure that evinces the densities of a large fraction of side chains, loops, and insertions. These features permitted unambiguous identification of all eight individual subunits, despite their sequence similarity. Independent biochemical near-neighbor analysis supports our cryo-EM derived TRiC subunit arrangement. We obtained a Cα backbone model for each subunit from an initial homology model refined against the cryo-EM density. A subsequently optimized atomic model for a subunit showed ~95% of the main chain dihedral angles in the allowable regions of the Ramachandran plot. The determination of the TRiC subunit arrangement opens the way to understand its unique function and mechanism. In particular, an unevenly distributed positively charged wall lining the closed folding chamber of TRiC differs strikingly from that of prokaryotic and archaeal chaperonins. These interior surface chemical properties likely play an important role in TRiC's cellular substrate specificity.