Structure guided studies of the interaction between PTP1B and JAK
- Author(s)
- Morris, R; Keating, N; Tan, C; Chen, H; Laktyushin, A; Saiyed, T; Liau, NPD; Nicola, NA; Tiganis, T; Kershaw, NJ; Babon, JJ;
- Details
- Publication Year 2023-06-14,Volume 6,Issue #1,Page 641
- Journal Title
- Communications Biology
- Publication Type
- Research article
- Abstract
- Protein Tyrosine Phosphatase 1B (PTP1B) is the prototypical protein tyrosine phosphatase and plays an essential role in the regulation of several kinase-driven signalling pathways. PTP1B displays a preference for bisphosphorylated substrates. Here we identify PTP1B as an inhibitor of IL-6 and show that, in vitro, it can dephosphorylate all four members of the JAK family. In order to gain a detailed understanding of the molecular mechanism of JAK dephosphorylation, we undertook a structural and biochemical analysis of the dephosphorylation reaction. We identified a product-trapping PTP1B mutant that allowed visualisation of the tyrosine and phosphate products of the reaction and a substrate-trapping mutant with a vastly decreased off-rate compared to those previously described. The latter mutant was used to determine the structure of bisphosphorylated JAK peptides bound to the enzyme active site. These structures revealed that the downstream phosphotyrosine preferentially engaged the active site, in contrast to the analogous region of IRK. Biochemical analysis confirmed this preference. In this binding mode, the previously identified second aryl binding site remains unoccupied and the non-substrate phosphotyrosine engages Arg47. Mutation of this arginine disrupts the preference for the downstream phosphotyrosine. This study reveals a previously unappreciated plasticity in how PTP1B interacts with different substrates.
- Publisher
- Springer Nature
- Keywords
- *Phosphoric Monoester Hydrolases; Phosphotyrosine; *Janus Kinases; Arginine; Binding Sites
- Department(s)
- Laboratory Research
- PubMed ID
- 37316570
- Publisher's Version
- https://doi.org/10.1038/s42003-023-05020-9
- Open Access at Publisher's Site
https://doi.org/10.1038/s42003-023-05020-9- Terms of Use/Rights Notice
- Refer to copyright notice on published article.
Creation Date: 2023-10-12 05:13:32
Last Modified: 2023-10-12 05:16:23