Researchers take a fresh look at the Michaelis-Menten equation

Move over Michaelis-Menten!
Magnus Kjærgaard (left) and Mateusz Dyla challenge one of the cornerstones of biochemistry, the Michaelis-Menten equation as they show that many enzymes in signaling pathways are independent of substrate concentration, because the substrate is physically connected to the enzyme. Credit: Mateusz Dyla

Researchers from Aarhus University challenge one of the cornerstones of biochemistry, the Michaelis-Menten equation. They show that many enzymes in signaling pathways are independent of substrate concentration, because the substrate is physically connected to the enzyme. With these results, it may one day be possible to develop drugs that not only target the enzyme, but also affect how it is connected to its substrate.

Cells send signals through cascades, where one enzyme passes the signal to the next. In such cascades, it is crucial that the enzyme recognizes the right substrates to ensure that, for example, a hormone activates the right cellular activities. Protein kinases, the enzymes in such cascades, are usually not sufficiently specific on their own, and therefore they rely on other proteins to physically connect them to the right substrates.

"Currently, we describe signaling enzymes with equations developed for metabolic enzymes," Magnus Kjærgaard explains. "Metabolic enzymes that make energy for our bodies, for example, need to process many substrates per minute. In contrast, signaling enzymes act as switches, and often only need to convert a single substrate to have an effect. Therefore, the equations developed to describe are less relevant for signaling enzymes."

For more than a hundred years, biochemists have described the activity of enzymes using the Michaelis-Menten equation, which describes how activity increases with increased substrate equation. When the enzyme is connected to its substrate, it does not matter how much substrate is present. Instead, the speed of the reaction depends on how the enzyme is connected to the substrate and thus on the connector molecule. Until now, we have not had any description of how the structure of such molecules affected enzymatic reactions.

"Normally, the question you are trying to answer is what graph shape describes the enzyme activity. We had a much more ," says first-author Mateusz Dyla. "What should we put on the X-axis instead of concentration?"

Connector molecules control cellular signaling

The authors made a model system where they could change the connection between the enzyme and the substrate. They used this to measure how the length of a flexible connector affects the first round of catalysis by the enzyme, which took place in milliseconds. Finally, they ended up with an equation that describes how the speed of the enzyme depends on the connection between enzyme and substrate. This suggested that connector molecules play an overlooked role in controlling cellular signaling.

The connection between enzyme and substrate also affects which substrates the enzyme prefers. Substrates that look similar can be very different when the enzyme only processes a single connected substrate.

"It is like the difference between how long it takes me to eat a single hotdog, and how many hotdogs I can eat over a whole week," Magnus explains. "Over the course of a week, I will be limited by how fast I can digest the hotdogs. This is irrelevant to the time it takes to eat the first hotdog. Therefore, the two types of measurements give different results. If you want to understand kinase switches, you have to focus on the first round of catalysis."

In the long-term, this may have implications for the development of drugs targeting kinases in, for example, cancer. Mateusz explains: "We hope that one day it will be possible to make drugs that not only target the enzyme, but also target how it is connected to its ."

The results have been published in the international journal PNAS.


Explore further

Paradigm-shifting theory highlights the importance of substrate flexibility in enzymatic reactions

More information: Mateusz Dyla and Magnus Kjaergaard. Intrinsically disordered linkers control tethered kinases via effective concentration. PNAS first published August 18, 2020. doi.org/10.1073/pnas.2006382117
Provided by Aarhus University
Citation: Researchers take a fresh look at the Michaelis-Menten equation (2020, August 20) retrieved 28 October 2020 from https://phys.org/news/2020-08-fresh-michaelis-menten-equation.html
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