New Type of Friction Discovered in Ligand-Protein Systems

- EN - DE
A team from the University of Freiburg and the Max Planck Institute of Biophysics in Frankfurt-am-Main identifies anisotropic friction

An interdisciplinary research team of the Institutes of Physical Chemistry and Physics of the University of Freiburg and the Max Planck Institute of Biophysics in Frankfurt-am-Main has discovered a new, direction-dependent friction in proteins called anisotropic friction. "Until now, nobody had observed that friction in biomolecules was dependent on direction," says physicist Dr. Steffen Wolf of the University of Freiburg. The results have been published as cover story in the scientific journal "Nano Letters."

Experiments on model complex of protein-ligands

Proteins constitute the microscopic machinery of cells. They perform work during their functional cycles. Accordingly, they follow the laws of thermodynamics, exhibit an energy conversion efficiency, and lose energy during their functional cycle due to dissipation. From a macroscopic perspective, the latter effect corresponds to apparent friction. On the microscopic scale of single proteins, a known source of friction is internal friction of proteins that results from the excitation of protein-internal vibrations. A further source is solvent friction, which arises from the acceleration of surrounding solvent molecules. These sources of friction lead to heating of both protein and solvent. Here, the researchers discovered the novel type of friction by carrying out single molecule experiments and simulations on a model complex of a protein and a ligand.

In their single molecule experiments, the team used a new method applying stereographic single molecule force spectroscopy, which is based on atomic force microscopy (AFM). This technique allowed them to study the unbinding of a ligand from a protein bound to a surface not only along a single coordinate, but along all three Cartesian coordinates. During their experiments, Dr. Wanhao Cai , Thorsten Hugel and Dr. Bizan N. Balzer of the Institute of Physical Chemistry of the University of Freiburg as well as Dr. Jakob T. Bullerjahn of the Max Planck Institute, made the surprising discovery that friction during ligand unbinding increases with the pulling angle applied.

Combining experiment and computer simulations

Miriam Jäger and Dr. Steffen Wolf of the University of Freiburg’s Institute of Physics subsequently recreated the experiment using computer simulations. They used the high performance computing (HPC) resources of the BinAC-HPC-Cluster in Tübingen. During the simulations they determined that the work of detaching a ligand from its binding site depends on the exact direction of application of the pulling force.

By combining results from the experiment and simulations, the researchers recognized that the source of the angle-dependent friction is the undefinable and random orientation of the proteins along their rotational axes bound to the surface in the experiment. The team repeated the single molecule pulling experiments by binding and unbinding a ligand to and from a protein many times in order to achieve statistically significant results. There, the ligand binds to a different protein for each measurement. Consequently, in each measurement, a ligand was pulled at the same angle with respect to the surface, but over different regions of the randomly-oriented protein. This orientation cannot be defined, both in the experimental setup and in the real world, and each measurement cannot be exactly and reversibly repeated. Therefore, each time different amounts of energy were deposited into the biomolecule. The irreversible part of this energy was lost as heat to the system. The corresponding effect is a source of friction, which the researchers call anisotropic friction.

A fundamental type of friction

"We assume that this previously unknown and fundamental type of friction is present in every bioassembly in which randomness in protein orientation appears together with directionality of force application," says Dr. Bizan N. Balzer , a biophysicist. He explains that this is the case in biomolecular motors or force-sensitive membrane proteins, as well as for processes such as blood flow, where forces are exerted on randomly oriented proteins. Balzer concludes, "Anisotropic friction is thus another important piece of the puzzle for understanding friction in both technical applications and in biological complexes in general."

Factual overview:

  • Original publication: Cai, W., Jäger, M., Bullerjahn, J. T., Hugel, T., Wolf, S., Balzer, B. N.: Anisotropic Friction in a Ligand-Protein Complex. In: Nano Letters 2023. DOI: http://doi.org/10.1021/a­cs.nanolet­t.2c04632.
  • Thorsten Hugel is a professor, Bizan N. Balzer a lecturer and Wanhao Cai a post-doctoral researcher at the Institute of Physical Chemistry of the University of Freiburg. Hugel and Balzer are members of the Excellence Cluster "Living Adaptive and Energy-autonomous Materials Systems" (livMatS) of the University of Freiburg. Balzer is a member of the Freiburg Materials Research Center (FMF). Steffen Wolf is a lecturer, and Miriam Jäger a doctoral candidate, at the Institute of Physics at the University of Freiburg. They are members of the Research Unit FOR5099 of the German Research Foundation (DFG) "Reducing complexity of nonequilibrium systems." Jakob T. Bullerjahn is a staff researcher at the Max Planck Institute of Biophysics in Frankfurt-am-Main.


  • The German Research Foundation (DFG) is supporting their research through the project HU 997/13-1, the excellence initiative - EXC-2193/1 - 390951807 and the project WO 2410/2-1 within the Research Unit FOR5099 "Reducing complexity of nonequilibrium systems" (project no. 431 945 604) and the project INST 37/935-1 FUGG, as well as the Max Planck Society. Furthermore,

    Pressefoto zum Download  

    Caption: Pulling experiments on a biotin-streptavidin complex. Biotin (blue lines) is pulled out of a streptavidin protein (yellow) via a polymer linker (gray line), which is bound to a cantilever tip of an atomic force microscope (gray triangle).