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Subject: SVY

Kanazawa University Research: Lipids and Proteins: Further Evidence for Functional Crosstalk in Cells


KANAZAWA, Japan, June 17, 2018 /PRNewswire/ --

Researchers at Kanazawa University have uncovered the role of lipids in facilitating a functional switch between two forms of a cellular enzyme: Peroxiredoxin (Prxs). Their study published in the Journal of Molecular Biology explains how negatively charged membrane lipids can bind to Prxs, and induce structural changes, in turn flipping their function.

     (Photo: https://mma.prnewswire.com/media/706938/Kanazawa_University_Lipids_and_Proteins_Infographic.jpg )

Kanazawa University WPI Nano Life Science Institute

https://nanolsi.kanazawa-u.ac.jp/en/

Prxs are a family of proteins found in abundance within red blood cells. The most common form of these, is 2-Cys Prxs. Until recently, the primary function of 2-Cys Prxs was thought to be its involvement in neutralizing free radicals, such as hydrogen peroxide (H2O2) which are harmful by-products of chemical reactions in the cell. Prxs have "active sites" on their surface, which can bind to free radicals and deactivate them.

A more ambiguous role of 2-Cys Prxs is that of a chaperone; essential in maintaining the structural composition of other proteins, especially under conditions of stress. To undertake this role, 2-Cys Prxs must be in arranged as high-molecular-weight complexes (HMW). In the native form, it is dimeric in structure. The only known inducers of HMWs, are a docking of the energy carrier ATP/ADP onto the dimer, or overoxidation, a chemical reaction in which the active site is blocked. The exact roles of these inducers are however, debatable. Takamitsu Haruyama and colleagues conducted a groundbreaking study on the process that causes 2-Cys Prxs to switch into chaperones, which until now was quite elusive.

The research team first grew the human form of 2-Cys Prxs, in bacteria, and isolated it. To then induce HMWs, it was incubated with Mg-ATP or Mg-ADP, their stable counterparts. Overoxidation was used as an alternative inducer. To their surprise, yields of HMWs were quite low. The structure of the resulting HMWs was examined using atomic force microscopy (AFM), a sophisticated technique used to magnify the structure of macromolecules. AFM suggested that HMWs consisted of a big sphere, which upon dismantling, revealed various shapes: a small hexagonal lattice, flattened sheets, and even smaller trefoil or clover-shaped particles. The team now had reason to believe that their isolated 2-Cys Prxs, was contaminated with something from the host bacteria, which lowered their yields, and formed spherical vesicles. This contamination was most likely to be another set of cellular macromolecules - lipids.

2-Cys Prxs was subsequently isolated with utmost care, ensuring it was free of all lipids. In a serendipitous discovery, the team now noticed that Mg-ADP or overoxidation no longer induced HMWs. Could it be the lipids then, that led to formation of HMWs? Four different membrane lipids were now incubated with 2-Cys Prxs. Two of these, phosphotidylglycerol (PG) and phosphotidylserine (PS) did indeed result in HMWs formation. This too had a nearly identical spherical structure, containing trefoil-shaped particles, most likely oligomers of 2-Cys Prxs. To assess functionality of the newly formed HMWs, their chaperone activity was tested on an artificially distressed protein. Indeed, only chaperone activity and no inherent peroxidase activity was seen.

The authors speculate the exact chaperone function of the HMWs in the context of stress. They hypothesize that this complex might play a role in capturing and removing incorrectly structured proteins from the cell, which would otherwise cause more damage. Although this hypothesis needs further validation, their discovery of the specific lipids involved in this mechanism, will make it much easier. Given the need for chaperones in combatting aging, neurodegenerative diseases and cancer, these findings could have an impact on therapeutic research.

References:

Takamitsu Haruyama, Takayuki Uchihashi, Yutaro Yamada, Noriyuki Kodera, Toshio Ando and Hiroki Konno, "Negatively Charged Lipids Are Essential for Functional and Structural Switch of Human 2-Cys Peroxiredoxin II", Journal of Molecular Biology (January 2018)

doi: https://doi.org/10.1016/j.jmb.2017.12.020

About WPI Nano Life Science Institute (WPI-NanoLSI), Kanazawa University

The Kanazawa University Nano Life Science Institute (WPI-NanoLSI) was launched October 2017 following the selection of The University for the World Premier International Research Initiative (WPI) by Japan's Ministry of Education, Culture, Sports, Science and Technology (MEXT).

The mission of the NanoLSI is to combine the world's foremost knowledge of bio-scanning probe microscopy and supramolecular chemistry to develop 'nano-endoscopic techniques' to directly image, analyze, and manipulate the nano-dynamics of proteins and nucleic acids both on the surface and inside of living cells. Notably, complementary experimental and multi-scale simulation techniques developed in this research will form a basis for elucidating wide ranging molecular and cellular dynamics by comparing healthy and cancer cells.

Based on the techniques and expertise gained through this process, Kanazawa University will create the new academic field of 'Nanoprobe Life Science', to promote fundamental understanding of critical mechanisms governing diverse life phenomena such as diseases and aging.

https://nanolsi.kanazawa-u.ac.jp/en/

Further information
Public Affairs
WPI Nano Life Science Institute (WPI-NanoLSI), Kanazawa University,  
Kakuma-machi, Kanazawa 920-1192, Japan
Email: nanolsi-office@adm.kanazawa-u.ac.jp
Tel: +81 (76) 234-4550



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