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30-Jun-2020

Kanazawa University Research: Real-time Monitoring of Proteins in the Nuclear Pore Complex

KANAZAWA,Japan, June 30, 2020 /PRNewswire/ -- Researchers at Kanazawa University report in Biomaterials a high-speed atomic-force microscopy study of protein filaments in the nuclear pore complex.  The visualization in real-time of the filaments' dynamics is an important step in our understanding of molecular transport mechanisms between a cell nucleus and its surrounding medium.

In human cells, the nucleus is enclosed by a structure called the nuclear pore complex (NPC).  It acts as a 'gatekeeper' controlling the transport of molecules between the nucleus and the surrounding cytoplasm (the protein-containing solution in the inside of a cell).  The NPC consists of proteins known as nucleoporins; some of these, the so-called FG-NUPs, belong to the class of intrinsically disordered proteins (IDPs) and capable of forming liquid-–liquid phase separation (LLPS), lacking a well-defined tertiary structure (that is, a particular 3D shape).  Although a lot is known about FG-NUPs, a thorough understanding of how their structure varies in time and space has been missing.  But now, by applying high-speed atomic force microscopy (HS-AFM), Richard Wong from Kanazawa University and colleagues provide much-needed insights into the spatiotemporal structure of FG-NUPs.

The technique used by the researchers, HS-AFM, is typically used for imaging surfaces.  A tiny cantilever is made to move over the surface; at any given time, the force experienced by the cantilever probe can be converted into a height measure.  A scan of the whole surface then results in a height map of the sample.  By repeatedly scanning the surface rapidly, a video of its evolving structure is obtained.  Applying HS-AFM to FG-NUPs, Wong and colleagues were able to measure several of the molecules' properties, including the extension velocity of FG-NUP filaments (thread-like protruding structures), their bending angles and how they form knots.

The scientists studied FG-NUPs in normal colon cells and in colorectal cancer cells and organoids.  They found that the former displayed less conformational dynamics.  A particularly interesting conclusion is that in colon cancer cells, the structure of the so-called central plug is smaller, and cannot develop filamentous features as easily as in normal cells, a finding with high clinical relevance.

The results of Wong and colleagues regarding the central plug are very important and timely, as its morphology and function have been the subject of debate.  The researchers now provide strong evidence that the central plug at least partially consists of FG-NUPs.

Apart from demonstrating that HS-AFM is a tool capable of visualizing FG-NUP filament motion in real time, another implication of the work of the scientists is "that bio-recycled nanomaterials [like NPC nanopores] … have biocompatible advantages … directly derived from cells and organoids, rather than other engineered nanomaterials [like e.g. carbon nanotubes, which may induce tumors and related pathologies] opening a new avenue for nano-tissue engineering."

Background

Nuclear pore complex

The nucleus of a cell is of key importance to any organism. It stores and organizes genetic information (DNA) in a way separating it from other cellular components in the surrounding cytoplasm.  The nuclear pore complex (NPC), a very large protein complex dressed around the nucleus, is the 'gatekeeper' in the exchange of molecules between the nucleus and the  cytoplasm; it lets material pass that should reach the nucleus and blocks material that should not.  This communication can happen because of pores in the NPC, structures built from proteins known as FG-NUPs.  FG-NUPs do not have well-defined shapes; instead, they vary in time and space.  By applying a technique called high-speed atomic force microscopy, Richard Wong from Kanazawa University and colleagues have now provided new, valuable insights into the spatiotemporal structure of FG-NUPs of both normal and cancer cells.

Atomic force microscopy

Atomic force microscopy (AFM) is an imaging technique in which the image is formed by scanning a surface with a very small tip.  Horizontal scanning motion of the tip is controlled via piezoelectric elements, while vertical motion is converted into a height profile, resulting in a height distribution of the sample's surface.  As the technique does not involve lenses, its resolution is not restricted by the so-called diffraction limit.  In a high-speed setup (HS-AFM), the method can be used to produce movies of a sample's structural evolution in real time.  Wong and colleagues have successfully used HS-AFM to study the dynamics of FG-NUPs, proteins playing a key role in the transport-regulating function of the nuclear pore complex situated between a cell's nucleus and the surrounding cytoplasm.

Reference

Mahmoud Shaaban Mohamed, Masaharu Hazawa, Akiko Kobayashi, Laurent Guillaud, Takahiro Watanabe-Nakayama, Mizuho Nakayama, Hanbo Wang, Noriyuki Kodera, Masanobu Oshima, Toshio Ando, and Richard W. Wong.  Spatiotemporally tracking of nano-biofilaments inside the nuclear pore complex core, Biomaterials Available online 23 June 2020.

DOI: https://doi.org/10.1016/j.biomaterials.2020.120198 

URL: https://www.sciencedirect.com/science/article/pii/S0142961220304440  

Figure 1.

https://nanolsi.kanazawa-u.ac.jp/wp-content/uploads/2020/06/Wong1.png

Caption: Schematic illustration of manipulation and tracking of native nuclear nano-pores from colon cancer cells and mouse organoids. Live tracking of single bio-filament conformations inside the nuclear pore presented as a nano diagnosis tool for the colorectal cancer.

Figure 2.

https://nanolsi.kanazawa-u.ac.jp/wp-content/uploads/2020/06/Wong2.png

Caption: HS-AFM enables dynamically studying filament structures in FG-NUP LLPS proteins, including twisting and knot formation.

About Nano Life Science Institute (WPI-NanoLSI)

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

Nano Life Science Institute (NanoLSI), Kanazawa University is a research center established in 2017 as part of the World Premier International Research Center Initiative of the Ministry of Education, Culture, Sports, Science and Technology. The objective of this initiative is to form world-tier research centers. NanoLSI combines the foremost knowledge of bio-scanning probe microscopy to establish 'nano-endoscopic techniques' to directly image, analyze, and manipulate biomolecules for insights into mechanisms governing life phenomena such as diseases.

About Institute for Frontier Science Initiative (InFiniti)

https://infiniti.adm.kanazawa-u.ac.jp/en/

Institute for Frontier Science Initiative (InFiniti) was established in April 2015 for the purpose of creating innovative research results and opening new fields of scientific inquiry. The Institute enhances the academic advantages of Kanazawa University, promotes interdisciplinary research, and accelerates international circulation of talented researchers. It also cultivates young researchers' interdisciplinarity, comprehensiveness, and internationality on the basis of its research results.

About Kanazawa University

http://www.kanazawa-u.ac.jp/e/

As the leading comprehensive university on the Sea of Japan coast, Kanazawa University has contributed greatly to higher education and academic research in Japan since it was founded in 1949. The University has three colleges and 17 schools offering courses in subjects that include medicine, computer engineering, and humanities.

The University is located on the coast of the Sea of Japan in Kanazawa – a city rich in history and culture. The city of Kanazawa has a highly respected intellectual profile since the time of the fiefdom (1598-1867). Kanazawa University is divided into two main campuses: Kakuma and Takaramachi for its approximately 10,200 students including 600 from overseas.

About WPI nanoLSI Kanazawa University

Hiroe Yoneda
Vice Director of 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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Last Updated: 30-Jun-2020