Evidence map›Paper›PMID 36032526›Full record

ArticleJACS Au2022

Recognizing the Binding Pattern and Dissociation Pathways of the p300 Taz2-p53 TAD2 Complex.

Tongtong Li, Stefano Motta, Amy O Stevens, Shenghan Song, Emily Hendrix, Alessandro Pandini, Yi He

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Article in JACS Au, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Tongtong LiDepartment of Chemistry & Chemical Biology, The University of New Mexico, Albuquerque, New Mexico 87131, United States.
Stefano MottaDepartment of Earth and Environmental Sciences, University of Milano-Bicocca, Milan 20126, Italy.ORCID https://orcid.org/0000-0002-0812-6834
Amy O StevensDepartment of Chemistry & Chemical Biology, The University of New Mexico, Albuquerque, New Mexico 87131, United States.
Shenghan SongDepartment of Chemistry & Chemical Biology, The University of New Mexico, Albuquerque, New Mexico 87131, United States.
Emily HendrixDepartment of Chemistry & Chemical Biology, The University of New Mexico, Albuquerque, New Mexico 87131, United States.
Alessandro PandiniDepartment of Computer Science, Brunel University London, Uxbridge UB8 3PH, U.K.ORCID https://orcid.org/0000-0002-4158-233X
Yi HeDepartment of Chemistry & Chemical Biology, The University of New Mexico, Albuquerque, New Mexico 87131, United States.ORCID https://orcid.org/0000-0002-6884-5312

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The dynamic association and dissociation between proteins are the basis of cellular signal transduction. This process becomes much more complicated if one or both interaction partners are intrinsically disordered because intrinsically disordered proteins can undergo disorder-to-order transitions upon binding to their partners. p53, a transcription factor with disordered regions, plays significant roles in many cellular signaling pathways. It is critical to understand the binding/unbinding mechanism involving these disordered regions of p53 at the residue level to reveal how p53 performs its biological functions. Here, we studied the dissociation process of the intrinsically disordered N-terminal transactivation domain 2 (TAD2) of p53 and the transcriptional adaptor zinc-binding 2 (Taz2) domain of transcriptional coactivator p300 using a combination of classical molecular dynamics, steered molecular dynamics, self-organizing maps, and time-resolved force distribution analysis (TRFDA). We observed two different dissociation pathways with different probabilities. One dissociation pathway starts from the TAD2 N-terminus and propagates to the α-helix and finally the C-terminus. The other dissociation pathway is in the opposite order. Subsequent TRFDA results reveal that key residues in TAD2 play critical roles. Besides the residues in agreement with previous experimental results, we also highlighted some other residues that play important roles in the disassociation process. In the dissociation process, non-native interactions were formed to partially compensate for the energy loss due to the breaking of surrounding native interactions. Moreover, our statistical analysis results of other experimentally determined complex structures involving either Taz2 or TAD2 suggest that the binding of the Taz2-TAD2 complex is mainly governed by the binding site of Taz2, which includes three main binding regions. Therefore, the complexes involving Taz2 may follow similar binding/unbinding behaviors, which could be studied together to generate common principles.

Identifiers

PMID36032526
PMCPMC9400049

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