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NOS1AP Interacts with α-Synuclein and Aggregates in Yeast and Mammalian Cells. / Matiiv, Anton B. ; Moskalenko , Svetlana E. ; Sergeeva, Olga S. ; Zhouravleva , Galina A. ; Bondarev , Stanislav A. .

In: International Journal of Molecular Sciences, Vol. 23, No. 16, 9102, 08.2022.

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@article{9e4dc9e41291492aacdcc9b0f8a7d4c3,
title = "NOS1AP Interacts with α-Synuclein and Aggregates in Yeast and Mammalian Cells",
abstract = "The NOS1AP gene encodes a cytosolic protein that binds to the signaling cascade component neuronal nitric oxide synthase (nNOS). It is associated with many different disorders, such as schizophrenia, post-traumatic stress disorder, autism, cardiovascular disorders, and breast cancer. The NOS1AP (also known as CAPON) protein mediates signaling within a complex which includes the NMDA receptor, PSD-95, and nNOS. This adapter protein is involved in neuronal nitric oxide (NO) synthesis regulation via its association with nNOS (NOS1). Our bioinformatics analysis revealed NOS1AP as an aggregation-prone protein, interacting with α-synuclein. Further investigation showed that NOS1AP forms detergent-resistant non-amyloid aggregates when overproduced. Overexpression of NOS1AP was found in rat models for nervous system injury as well as in schizophrenia patients. Thus, we can assume for the first time that the molecular mechanisms underlying these disorders include misfolding and aggregation of NOS1AP. We show that NOS1AP interacts with α-synuclein, allowing us to suggest that this protein may be implicated in the development of synucleinopathies and that its aggregation may explain the relationship between Parkinson{\textquoteright}s disease and schizophrenia.",
keywords = "NOS1AP, CAPON, α-synuclein, protein aggregation, schizophrenia, synucleinopathies, Rats, Synucleinopathies, Adaptor Proteins, Signal Transducing/metabolism, Signal Transduction/physiology, Animals, Saccharomyces cerevisiae/metabolism, Neurons/metabolism, Nitric Oxide Synthase Type I, alpha-Synuclein/genetics",
author = "Matiiv, {Anton B.} and Moskalenko, {Svetlana E.} and Sergeeva, {Olga S.} and Zhouravleva, {Galina A.} and Bondarev, {Stanislav A.}",
note = "Publisher Copyright: {\textcopyright} 2022 by the authors.",
year = "2022",
month = aug,
doi = "10.3390/ijms23169102",
language = "English",
volume = "23",
journal = "International Journal of Molecular Sciences",
issn = "1422-0067",
publisher = "MDPI AG",
number = "16",

}

RIS

TY - JOUR

T1 - NOS1AP Interacts with α-Synuclein and Aggregates in Yeast and Mammalian Cells

AU - Matiiv, Anton B.

AU - Moskalenko , Svetlana E.

AU - Sergeeva, Olga S.

AU - Zhouravleva , Galina A.

AU - Bondarev , Stanislav A.

N1 - Publisher Copyright: © 2022 by the authors.

PY - 2022/8

Y1 - 2022/8

N2 - The NOS1AP gene encodes a cytosolic protein that binds to the signaling cascade component neuronal nitric oxide synthase (nNOS). It is associated with many different disorders, such as schizophrenia, post-traumatic stress disorder, autism, cardiovascular disorders, and breast cancer. The NOS1AP (also known as CAPON) protein mediates signaling within a complex which includes the NMDA receptor, PSD-95, and nNOS. This adapter protein is involved in neuronal nitric oxide (NO) synthesis regulation via its association with nNOS (NOS1). Our bioinformatics analysis revealed NOS1AP as an aggregation-prone protein, interacting with α-synuclein. Further investigation showed that NOS1AP forms detergent-resistant non-amyloid aggregates when overproduced. Overexpression of NOS1AP was found in rat models for nervous system injury as well as in schizophrenia patients. Thus, we can assume for the first time that the molecular mechanisms underlying these disorders include misfolding and aggregation of NOS1AP. We show that NOS1AP interacts with α-synuclein, allowing us to suggest that this protein may be implicated in the development of synucleinopathies and that its aggregation may explain the relationship between Parkinson’s disease and schizophrenia.

AB - The NOS1AP gene encodes a cytosolic protein that binds to the signaling cascade component neuronal nitric oxide synthase (nNOS). It is associated with many different disorders, such as schizophrenia, post-traumatic stress disorder, autism, cardiovascular disorders, and breast cancer. The NOS1AP (also known as CAPON) protein mediates signaling within a complex which includes the NMDA receptor, PSD-95, and nNOS. This adapter protein is involved in neuronal nitric oxide (NO) synthesis regulation via its association with nNOS (NOS1). Our bioinformatics analysis revealed NOS1AP as an aggregation-prone protein, interacting with α-synuclein. Further investigation showed that NOS1AP forms detergent-resistant non-amyloid aggregates when overproduced. Overexpression of NOS1AP was found in rat models for nervous system injury as well as in schizophrenia patients. Thus, we can assume for the first time that the molecular mechanisms underlying these disorders include misfolding and aggregation of NOS1AP. We show that NOS1AP interacts with α-synuclein, allowing us to suggest that this protein may be implicated in the development of synucleinopathies and that its aggregation may explain the relationship between Parkinson’s disease and schizophrenia.

KW - NOS1AP

KW - CAPON

KW - α-synuclein

KW - protein aggregation

KW - schizophrenia

KW - synucleinopathies

KW - Rats

KW - Synucleinopathies

KW - Adaptor Proteins, Signal Transducing/metabolism

KW - Signal Transduction/physiology

KW - Animals

KW - Saccharomyces cerevisiae/metabolism

KW - Neurons/metabolism

KW - Nitric Oxide Synthase Type I

KW - alpha-Synuclein/genetics

UR - http://www.scopus.com/inward/record.url?scp=85136703224&partnerID=8YFLogxK

UR - https://www.mendeley.com/catalogue/b96765ba-6a45-36b6-8b98-4e6bf41ae912/

U2 - 10.3390/ijms23169102

DO - 10.3390/ijms23169102

M3 - Article

C2 - 36012368

VL - 23

JO - International Journal of Molecular Sciences

JF - International Journal of Molecular Sciences

SN - 1422-0067

IS - 16

M1 - 9102

ER -

ID: 99683743