News Release 

A small twist leads to a big reaction

Key components of proteins are twisted to boost reactions useful to medicine

University of Tokyo

IMAGE

IMAGE: These act as advanced catalysts to speed up the hydrolysis of amide bonds. view more 

Credit: © 2020 Fujita et al.

In proteins, amino acids are held together by amide bonds. These bonds are long-lived and are robust against changes in temperature, acidity or alkalinity. Certain medicines make use of reactions involving amide bonds, but the bonds are so strong they actually slow down reactions, impeding the effectiveness of the medicines. Researchers devised a way to modify amide bonds with a twist to their chemical structure that speeds up reactions by 14 times.

The amide bonds that hold amino acids in place to form proteins ordinarily have a flat shape, said to be planar. This planar arrangement is known to give amide bonds their incredible resilience to change. So if a reaction requires a breakdown of amide bonds, it's going to have a hard time unless it gets some help.

One such reaction is called hydrolysis, a chemical breakdown due to the presence of water. This is used by some medicines, for example antibiotics, within the body. Hydrolysis is also used in the lab as a tool for chemical analysis, amongst other things. So if hydrolysis can be made faster, it could benefit research in these areas. And this is exactly what Professor Makoto Fujita and his team at the Department of Applied Chemistry have done.

"Amide bonds can be hydrolyzed in time given sufficient heat or pH balance, but this can be inefficient or expensive at scale," said Fujita. "For many years we have fabricated self-assembling molecular cage structures which can confine and modify structures within them. In this case, we confined amide bonds in molecular cages which then applied a slight twist of 34 degrees to their otherwise planar structures. And the results are encouraging."

What Fujita and his team discovered was that given this slight twist in their structures, amide bonds were able to be hydrolyzed at a much faster rate with certain configurations, increasing their reaction rate by up to 14 times. This could be of great benefit to various medical researchers in the fields of drug development and more besides.

###

Journal article

Hiroki Takezawa, Kosuke Shitozawa & Makoto Fujita. Enhanced reactivity of twisted amides inside a molecular cage. Nature Chemistry. DOI: 10.1038/s41557-020-0455-y https://www.nature.com/articles/s41557-020-0455-y

This research was supported by Grants-in-Aid for Specially Promoted Research (19H05461 to M.F.), for Young Scientists (19K15581 to H.T.) and the Noguchi Institute (to H.T.).

Related links

Department of Applied Chemistry
https://www.appchem.t.u-tokyo.ac.jp/en/

Graduate School of Engineering
https://www.t.u-tokyo.ac.jp/soee/

Institute for Molecular Science (NINS)
https://www.ims.ac.jp/en/

Research Contact

Professor Makoto Fujita
Department of Applied Chemistry, The University of Tokyo
7-3-1 Hongo, Tokyo 113-0033, JAPAN
Tel: +81-3-5841-7259 - Email: mfujita@appchem.t.u-tokyo.ac.jp

Press Contact

Mr. Rohan Mehra
Division for Strategic Public Relations, The University of Tokyo
7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8654, JAPAN
Tel: +81-3-5841-0876 - Email: press-releases.adm@gs.mail.u-tokyo.ac.jp

About the University of Tokyo

The University of Tokyo is Japan's leading university and one of the world's top research universities. The vast research output of some 6,000 researchers is published in the world's top journals across the arts and sciences. Our vibrant student body of around 15,000 undergraduate and 15,000 graduate students includes over 4,000 international students. Find out more at https://www.u-tokyo.ac.jp/en/ or follow us on Twitter at @UTokyo_News_en.

Disclaimer: AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert system.