TY - JOUR
T1 - Site-specific phosphorylation of PSD-95 dynamically regulates the postsynaptic density as observed by phase separation
AU - Vistrup-Parry, Maria
AU - Chen, Xudong
AU - Johansen, Thea L.
AU - Bach, Sofie
AU - Buch-Larsen, Sara C.
AU - Bartling, Christian R.O.
AU - Ma, Chenxue
AU - Clemmensen, Louise S.
AU - Nielsen, Michael L.
AU - Zhang, Mingjie
AU - Strømgaard, Kristian
N1 - Publisher Copyright:
© 2021 The Authors
PY - 2021/11/19
Y1 - 2021/11/19
N2 - Postsynaptic density protein 95 is a key scaffolding protein in the postsynaptic density of excitatory glutamatergic neurons, organizing signaling complexes primarily via its three PSD-95/Discs-large/Zona occludens domains. PSD-95 is regulated by phosphorylation, but technical challenges have limited studies of the molecular details. Here, we genetically introduced site-specific phosphorylations in single, tandem, and full-length PSD-95 and generated a total of 11 phosphorylated protein variants. We examined how these phosphorylations affected binding to known interaction partners and the impact on phase separation of PSD-95 complexes and identified two new phosphorylation sites with opposing effects. Phosphorylation of Ser78 inhibited phase separation with the glutamate receptor subunit GluN2B and the auxiliary protein stargazin, whereas phosphorylation of Ser116 induced phase separation with stargazin only. Thus, by genetically introducing phosphoserine site-specifically and exploring the impact on phase separation, we have provided new insights into the regulation of PSD-95 by phosphorylation and the dynamics of the PSD.
AB - Postsynaptic density protein 95 is a key scaffolding protein in the postsynaptic density of excitatory glutamatergic neurons, organizing signaling complexes primarily via its three PSD-95/Discs-large/Zona occludens domains. PSD-95 is regulated by phosphorylation, but technical challenges have limited studies of the molecular details. Here, we genetically introduced site-specific phosphorylations in single, tandem, and full-length PSD-95 and generated a total of 11 phosphorylated protein variants. We examined how these phosphorylations affected binding to known interaction partners and the impact on phase separation of PSD-95 complexes and identified two new phosphorylation sites with opposing effects. Phosphorylation of Ser78 inhibited phase separation with the glutamate receptor subunit GluN2B and the auxiliary protein stargazin, whereas phosphorylation of Ser116 induced phase separation with stargazin only. Thus, by genetically introducing phosphoserine site-specifically and exploring the impact on phase separation, we have provided new insights into the regulation of PSD-95 by phosphorylation and the dynamics of the PSD.
KW - Biochemistry
KW - Biomolecules
KW - Biophysical chemistry
KW - Biophysics
KW - Protein structure aspects
UR - https://www.webofscience.com/wos/woscc/full-record/WOS:000730109700008
UR - https://openalex.org/W3207741203
UR - https://www.scopus.com/pages/publications/85122617083
U2 - 10.1016/j.isci.2021.103268
DO - 10.1016/j.isci.2021.103268
M3 - Journal Article
SN - 2589-0042
VL - 24
JO - iScience
JF - iScience
IS - 11
M1 - 103268
ER -