Non-microtubule tubulin-based backbone and subordinate components of postsynaptic density lattices

Author:

Suzuki Tatsuo1ORCID,Terada Nobuo2,Higashiyama Shigeki3,Kametani Kiyokazu4,Shirai Yoshinori1ORCID,Honda Mamoru5,Kai Tsutomu5,Li Weidong67,Tabuchi Katsuhiko18ORCID

Affiliation:

1. Department of Molecular and Cellular Physiology, Shinshu University Academic Assembly, Institute of Medicine, Shinshu University Academic Assembly, Matsumoto, Japan

2. Health Science Division, Department of Medical Sciences, Graduate School of Medicine, Science and Technology, Shinshu University, Matsumoto, Nagano, Japan

3. Department of Cell Growth and Tumor Regulation, Proteo-Science Center, Ehime University, To-on, Ehime, Japan

4. Department of Veterinary Anatomy, Faculty of Veterinary Medicine, Rakuno Gakuen University, Ebetsu, Japan

5. Bioscience Group, Center for Precision Medicine Supports, Pharmaceuticals and Life Sciences Division, Shimadzu Techno-Research, INC, Kyoto, Japan

6. Bio-X Institutes, Key Laboratory for the Genetics of Development and Neuropsychiatric Disorders (Ministry of Education), Shanghai Key Laboratory of Psychotic Disorders, and Brain Science and Technology Research Center, Shanghai Jiao Tong University, Shanghai, China

7. Institute for Biomedical Sciences, Interdisciplinary Cluster for Cutting Edge Research Shinshu University, Matsumoto, Japan

8. Department of Biological Sciences for Intractable Neurological Diseases, Institute for Biomedical Sciences, Interdisciplinary Cluster for Cutting Edge Research Shinshu University, Matsumoto, Japan

Abstract

A purification protocol was developed to identify and analyze the component proteins of a postsynaptic density (PSD) lattice, a core structure of the PSD of excitatory synapses in the central nervous system. “Enriched”- and “lean”-type PSD lattices were purified by synaptic plasma membrane treatment to identify the protein components by comprehensive shotgun mass spectrometry and group them into minimum essential cytoskeleton (MEC) and non-MEC components. Tubulin was found to be a major component of the MEC, with non-microtubule tubulin widely distributed on the purified PSD lattice. The presence of tubulin in and around PSDs was verified by post-embedding immunogold labeling EM of cerebral cortex. Non-MEC proteins included various typical scaffold/adaptor PSD proteins and other class PSD proteins. Thus, this study provides a new PSD lattice model consisting of non-microtubule tubulin-based backbone and various non-MEC proteins. Our findings suggest that tubulin is a key component constructing the backbone and that the associated components are essential for the versatile functions of the PSD.

Funder

Grant from Institute of Medicine, Shinshu University Academic Assembly

Publisher

Life Science Alliance, LLC

Subject

Health, Toxicology and Mutagenesis,Plant Science,Biochemistry, Genetics and Molecular Biology (miscellaneous),Ecology

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