Non-Reciprocal Interactions Between Single Molecules Without External Forces Discovered

Category Physics

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Scientists have discovered a new mechanism by which single molecules can interact in a non-reciprocal manner without the use of external forces. Researchers from the University of Maine and Penn State explained this process is facilitated by the kinetic asymmetry of chemical catalysts, and may have played a role in the development of complex matter from simple matter.


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Scientists have found that molecules can interact in a non-reciprocal manner without external forces, a discovery that could change our understanding of molecular interactions and the evolution of life.

Researchers from the University of Maine and Penn State discovered that molecules experience non-reciprocal interactions without external forces.

Fundamental forces such as gravity and electromagnetism are reciprocal, where two objects are attracted to each other or are repelled by each other. In our everyday experience, however, interactions don’t seem to follow this reciprocal law. For example, a predator is attracted to prey, but the prey tends to flee from the predator. Such non-reciprocal interactions are essential for complex behavior associated with living organisms.

The kinetic asymmetry that allows these interactions is known as a property of enzymes, and can be found in many biological molecules

For microscopic systems such as bacteria, the mechanism of non-reciprocal interactions has been explained by hydrodynamic or other external forces, and it was previously thought that similar types of forces could explain interactions between single molecules.

In work published in the prestigious Cell Press journal Chem, UMaine theoretical physicist R. Dean Astumian and collaborators Ayusman Sen and Niladri Sekhar Mandal at Penn State have published a different mechanism by which single molecules can interact non-reciprocally without hydrodynamic effects.

The research builds on earlier work which showed that a catalyst molecule can use energy from a reaction it induces to move directionally in a concentration gradient

This mechanism invokes the local gradients of reactants and products due to the reactions facilitated by every chemical catalyst, a biological example of which is an enzyme. Because the response of a catalyst to the gradient depends on the catalyst’s properties, it is possible to have a situation in which one molecule is repelled by, but attracts, another molecule.

The authors’ “Eureka moment” occurred when, in their discussion, they realized that a property of every catalyst known as the kinetic asymmetry controls the direction of response to a concentration gradient. Because kinetic asymmetry is a property of the enzyme itself, it can undergo evolution and adaptation. The non-reciprocal interactions allowed by kinetic asymmetry also play a crucial role in allowing molecules to interact with each other, and may have played a critical role in the processes by which simple matter becomes complex.

The new mechanism of non-reciprocal interactions could change our understanding of molecular interactions and its role in the evolution of life

Much previous work has been done by other researchers on what happens when non-reciprocal interactions occur. These efforts have played a central role in the development of a field known as “active matter.” In this earlier work, the non-reciprocal interactions were introduced by incorporation of ad hoc forces.

The research described by Mandal, Sen, and Astumian, however, describes a basic molecular mechanism by which such interactions can arise between single molecules. This research builds on earlier work in which the same authors showed how a single catalyst molecule could use energy from the reaction it catalyzed to undergo directional motion in a concentration gradient.

This research was published in the prestigious Cell Press journal Chem

The kinetic asymmetry that features in determining the non-reciprocal interactions between different catalysts has also been shown to be important for the directionality of biomolocules in living organisms as well as to guide a single biomolecule using only local gradients of its own.


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