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Enhancing the population of the encounter complex affects protein complex formation efficiency
Author(s) -
Di Savino Antonella,
Foerster Johannes M.,
Ullmann G. Matthias,
Ubbink Marcellus
Publication year - 2022
Publication title -
the febs journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 204
eISSN - 1742-4658
pISSN - 1742-464X
DOI - 10.1111/febs.16159
Subject(s) - cytochrome c , cytochrome c peroxidase , peroxidase , cytochrome , chemistry , population , mutant , static electricity , wild type , stereochemistry , crystallography , biophysics , biochemistry , biology , enzyme , physics , mitochondrion , demography , quantum mechanics , sociology , gene
Optimal charge distribution is considered to be important for efficient formation of protein complexes. Electrostatic interactions guide encounter complex formation that precedes the formation of an active protein complex. However, disturbing the optimized distribution by introduction of extra charged patches on cytochrome c peroxidase does not lead to a reduction in productive encounters with its partner cytochrome c . To test whether a complex with a high population of encounter complex is more easily affected by suboptimal charge distribution, the interactions of cytochrome c mutant R13A with wild‐type cytochrome c peroxidase and a variant with an additional negative patch were studied. The complex of the peroxidase and cytochrome c R13A was reported to have an encounter state population of 80%, compared to 30% for the wild‐type cytochrome c . NMR analysis confirms the dynamic nature of the interaction and demonstrates that the mutant cytochrome c samples the introduced negative patch. Kinetic experiments show that productive complex formation is fivefold to sevenfold slower at moderate and high ionic strength values for cytochrome c R13A but the association rate is not affected by the additional negative patch on cytochrome c peroxidase, showing that the total charge on the protein surface can compensate for less optimal charge distribution. At low ionic strength (44 m m ), the association with the mutant cytochrome c reaches the same high rates as found for wild‐type cytochrome c , approaching the diffusion limit.