Cited by 92Neuroscience and Neuropharmacology ResearchGenetics and Neurodevelopmental DisordersProtein Kinase Regulation and GTPase Signaling

Scaffold Proteins at the Postsynaptic Density

Verpelli, Chiara, Schmeisser, Michael J., Sala, Carlo, Boeckers, Tobias M.·2012·Advances in Experimental Medicine and Biology

Abstract

Scaffold proteins are abundant and essential components of the postsynaptic density (PSD). They play a major role in many synaptic functions including the trafficking, anchoring, and clustering of glutamate receptors and adhesion molecules. Moreover, they link postsynaptic receptors with their downstream signaling proteins and regulate the dynamics of cytoskeletal structures. By definition, PSD scaffold proteins do not have intrinsic enzymatic activities but are formed by modular and specific domains deputed to form large protein networks. Here, we will discuss the latest findings regarding the structure and functions of major PSD scaffold proteins. Given that scaffold proteins are central components of PSD architecture, it is not surprising that deletion or mutations in their human genes cause severe neuropsychiatric disorders including autism, mental retardation, and schizophrenia. Thus, their dynamic organization and regulation are directly correlated with the essential structure of the PSD and the normal physiology of neuronal synapses.

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Crossref · 10.1007/978-3-7091-0932-8_2

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  • MAGUK family scaffold proteins are central to synaptic architecture, linking receptors to signaling cascades.

    “MAGUK family scaffold proteins are central to this architecture, linking receptors to signaling cascades; their dysfunction is a convergent factor in neuropsychiatric disorders such as autism and schizophrenia [56,85].”

    From Molecular Physiology of the Neuronal Synapse (2026) · cites this paper as [85]

  • Dysfunction of MAGUK family scaffold proteins is a convergent factor in neuropsychiatric disorders such as autism and schizophrenia.

    “MAGUK family scaffold proteins are central to this architecture, linking receptors to signaling cascades; their dysfunction is a convergent factor in neuropsychiatric disorders such as autism and schizophrenia [56,85].”

    From Molecular Physiology of the Neuronal Synapse (2026) · cites this paper as [85]

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References 235 · Cited by 92

Authors
Verpelli, C., Schmeisser, M. J., Sala, C., & Boeckers, T. M.
Affiliations
  • University of Milan (IT)
  • Universität Ulm (DE)
Corresponding author
  • Sala, Carlo
  • Boeckers, Tobias M.
Venue
Advances in Experimental Medicine and Biology
Published
2012
Volume
970
Pages
29-61
ISSN
0065-2598 (ISSN-L)
OpenAlex
W1881638195
Cited by
92
References
235
Citations by year
2026: 2 · 2025: 9 · 2024: 5 · 2023: 2 · 2022: 8 · 2021: 6 · 2020: 8 · 2019: 3 · 2018: 8 · 2017: 5 · 2016: 6 · 2015: 10 · 2014: 8 · 2013: 10 · 2012: 2
FWCI
10.57
Type
book chapter
Language
en
Open access
closed
Locations
  • Advances in experimental medicine and biology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
Keywords
postsynaptic density, scaffold proteins, synaptic organization, glutamate receptor trafficking, adhesion molecules, cytoskeletal dynamics, protein signaling networks, neuropsychiatric disorders, autism spectrum disorder, intellectual disability, schizophrenia
MeSH terms
Animals, Carrier Proteins, Cytoskeleton, Humans, Mice, Transgenic, Nerve Tissue Proteins, Synaptic Transmission, Neuronal Plasticity, Neurons, Protein Binding, Receptors, Glutamate, Glutamic Acid, Mice, Post-Synaptic Density

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