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. 2023 Jan 9;12:1. doi: 10.1186/s40035-022-00334-w

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© The Author(s) 2023

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 2 — p85S6K interacts with GluA1 specifically. a Co-immunoprecipitation of AMPA receptors in hippocampal tissue lysates with Flag-p85S6K or empty vector (Mock) from HEK293 cell lysates. b Co-immunoprecipitation of myc-GluA1 or myc-GluA2 with Flag-p85S6K, with AKAP79 co-transfected in HEK293 cells. c Co-immunoprecipitation results for Flag-p85S6K or Flag-p70S6K with myc-GluA1, with AKAP79 co-transfected in HEK293 cells. d, e Co-immunoprecipitation of endogenous GluA1 with p85S6K in the PSD-1 fraction. f Confirmation of such interaction in vivo by in situ PLA. Scale bar, 10 μm. Representative blots or images of at least 3 independent experiments are shown. IP immunoprecipitation, IB immunoblot