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-Structure paper
タイトル | Structural visualization of the tubulin folding pathway directed by human chaperonin TRiC/CCT. |
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ジャーナル・号・ページ | Cell, Vol. 185, Issue 25, Page 4770-4787.e20, Year 2022 |
掲載日 | 2022年12月8日 |
著者 | Daniel Gestaut / Yanyan Zhao / Junsun Park / Boxue Ma / Alexander Leitner / Miranda Collier / Grigore Pintilie / Soung-Hun Roh / Wah Chiu / Judith Frydman / |
PubMed 要旨 | The ATP-dependent ring-shaped chaperonin TRiC/CCT is essential for cellular proteostasis. To uncover why some eukaryotic proteins can only fold with TRiC assistance, we reconstituted the folding of ...The ATP-dependent ring-shaped chaperonin TRiC/CCT is essential for cellular proteostasis. To uncover why some eukaryotic proteins can only fold with TRiC assistance, we reconstituted the folding of β-tubulin using human prefoldin and TRiC. We find unstructured β-tubulin is delivered by prefoldin to the open TRiC chamber followed by ATP-dependent chamber closure. Cryo-EM resolves four near-atomic-resolution structures containing progressively folded β-tubulin intermediates within the closed TRiC chamber, culminating in native tubulin. This substrate folding pathway appears closely guided by site-specific interactions with conserved regions in the TRiC chamber. Initial electrostatic interactions between the TRiC interior wall and both the folded tubulin N domain and its C-terminal E-hook tail establish the native substrate topology, thus enabling C-domain folding. Intrinsically disordered CCT C termini within the chamber promote subsequent folding of tubulin's core and middle domains and GTP-binding. Thus, TRiC's chamber provides chemical and topological directives that shape the folding landscape of its obligate substrates. |
リンク | Cell / PubMed:36493755 / PubMed Central |
手法 | EM (単粒子) |
解像度 | 2.9 - 3.85 Å |
構造データ | EMDB-26089, PDB-7trg: EMDB-26120, PDB-7ttn: EMDB-26123, PDB-7ttt: EMDB-26131, PDB-7tub: EMDB-32822: An apo TRiC map EMDB-32823, PDB-7wu7: |
化合物 | ChemComp-MG: ChemComp-ADP: ChemComp-AF3: ChemComp-HOH: |
由来 |
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キーワード | CHAPERONE / Human chaperonin TRiC with beta-tubulin folding intermediate I / Human chaperonin TRiC with beta-tubulin folding intermediate II / Human chaperonin TRiC with beta-tubulin folding intermediate III / Human chaperonin TRiC with beta-tubulin folding intermediate IV / chapronin complex |