TY - JOUR
T1 - Using coarse-grained simulations to characterize the mechanisms of protein–protein association
AU - Dhusia, Kalyani
AU - Su, Zhaoqian
AU - Wu, Yinghao
N1 - Funding Information:
Funding: This work was supported by the National Institutes of Health under Grant Numbers R01GM120238 and R01GM122804. The work is also partially supported by a start‐up grant from Albert Einstein College of Medicine. Computational support was provided by Albert Einstein College of Medicine High Performance Computing Center.
Funding Information:
This work was supported by the National Institutes of Health under Grant Numbers R01GM120238 and R01GM122804. The work is also partially supported by a start-up grant from Albert Einstein College of Medicine. Computational support was provided by Albert Einstein College of Medicine High Performance Computing Center.
Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2020
Y1 - 2020
N2 - The formation of functionally versatile protein complexes underlies almost every biological process. The estimation of how fast these complexes can be formed has broad implications for unravelling the mechanism of biomolecular recognition. This kinetic property is traditionally quantified by association rates, which can be measured through various experimental techniques. To complement these time-consuming and labor-intensive approaches, we developed a coarse-grained simulation approach to study the physical processes of protein–protein association. We systematically calibrated our simulation method against a large-scale benchmark set. By combining a physics-based force field with a statistically-derived potential in the simulation, we found that the association rates of more than 80% of protein complexes can be correctly predicted within one order of magnitude relative to their experimental measurements. We further showed that a mixture of force fields derived from complementary sources was able to describe the process of protein–protein association with mechanistic details. For instance, we show that association of a protein complex contains multiple steps in which proteins continuously search their local binding orientations and form non-native-like intermediates through repeated dissociation and re-association. Moreover, with an ensemble of loosely bound encounter complexes observed around their native conformation, we suggest that the transition states of protein–protein association could be highly diverse on the structural level. Our study also supports the idea in which the association of a protein complex is driven by a “funnel-like” energy landscape. In summary, these results shed light on our understanding of how protein–protein recognition is kinetically modulated, and our coarse-grained simulation approach can serve as a useful addition to the existing experimental approaches that measure protein–protein association rates.
AB - The formation of functionally versatile protein complexes underlies almost every biological process. The estimation of how fast these complexes can be formed has broad implications for unravelling the mechanism of biomolecular recognition. This kinetic property is traditionally quantified by association rates, which can be measured through various experimental techniques. To complement these time-consuming and labor-intensive approaches, we developed a coarse-grained simulation approach to study the physical processes of protein–protein association. We systematically calibrated our simulation method against a large-scale benchmark set. By combining a physics-based force field with a statistically-derived potential in the simulation, we found that the association rates of more than 80% of protein complexes can be correctly predicted within one order of magnitude relative to their experimental measurements. We further showed that a mixture of force fields derived from complementary sources was able to describe the process of protein–protein association with mechanistic details. For instance, we show that association of a protein complex contains multiple steps in which proteins continuously search their local binding orientations and form non-native-like intermediates through repeated dissociation and re-association. Moreover, with an ensemble of loosely bound encounter complexes observed around their native conformation, we suggest that the transition states of protein–protein association could be highly diverse on the structural level. Our study also supports the idea in which the association of a protein complex is driven by a “funnel-like” energy landscape. In summary, these results shed light on our understanding of how protein–protein recognition is kinetically modulated, and our coarse-grained simulation approach can serve as a useful addition to the existing experimental approaches that measure protein–protein association rates.
KW - Coarse-grained simulations
KW - Physics-based force field
KW - Protein-protein association
KW - Statistical potential
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U2 - 10.3390/biom10071056
DO - 10.3390/biom10071056
M3 - Article
C2 - 32679892
AN - SCOPUS:85088050290
SN - 2218-273X
VL - 10
SP - 1
EP - 21
JO - Biomolecules
JF - Biomolecules
IS - 7
M1 - 1056
ER -