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Updated: Jun 23, 2026

Comparing the Affinity of GTPase-binding Proteins using Competition Assays
Published on: October 8, 2015
The charge-dipole pocket: a defining feature of signaling pathway GTPase on/off switches
1Institute for Genome Sciences and Department of Biochemistry & Molecular Biology, University of Maryland School of Medicine, Baltimore, 21201, USA. aneuwald@som.umaryland.edu
Abstract:
Ras-like GTPases function as on/off switches in intracellular signaling pathways. Their on or off state is communicated through conformational changes in the so-called switch I and II regions. It is commonly believed that the distinguishing molecular features of these GTPases are well known. Here, however, I identify-through a Bayesian iterative analysis of GTPase evolutionary divergence-a previously undescribed switch II structural component that (along with previously described, functionally critical residues) most distinguish these signaling pathway on/off switches from other GTPases. In certain Ras-like GTPases this newly-identified component forms an aromatic pocket around the negative-dipole moment at the end of a switch II helix with a positively charged residue inserted into the pocket. This helix is oriented in a specific direction away from the GTPase core, but is reoriented dramatically upon disruption of the charge-dipole pocket. The charge-dipole pocket occurs in both the on and off states and both the charge-dipole pocket and an alternative configuration occur within the unit cell of a single crystal structure of Rab5a GTPase in the off state. Thus, the charge-dipole pocket configuration is closely associated, not with the on or off state, but rather with formation of the outward-oriented helix and, as a result, with restructuring of the switch II N-terminal region, which has a critical role both in sensing the on/off state and in mediating GTP hydrolysis and nucleotide exchange.
Insights
Researchers discovered a new structural component in Ras-like GTPases, crucial for signaling pathway regulation. This finding refines our understanding of these molecular switches and their function.
Area of Science:
- Molecular Biology
- Biochemistry
- Structural Biology
Background:
- Ras-like GTPases act as molecular switches in cellular signaling.
- Their function relies on conformational changes in switch I and II regions.
- Existing knowledge suggests these GTPase features are well-understood.
Purpose of the Study:
- To identify novel structural components that distinguish Ras-like GTPases.
- To elucidate the role of these components in GTPase signaling.
- To challenge the established understanding of GTPase molecular features.
Main Methods:
- Bayesian iterative analysis of GTPase evolutionary divergence.
- Structural analysis of GTPase conformations.
- Investigation of charge-dipole interactions within switch II.
Main Results:
- A previously undescribed switch II structural component was identified.
- This component forms a charge-dipole pocket involving aromatic residues and a positive charge.
- The pocket's disruption reorients a key helix, impacting switch II restructuring.
Conclusions:
- The identified charge-dipole pocket is crucial for switch II restructuring and helix orientation.
- This pocket is associated with helix reorientation, not directly with the GTPase on/off state.
- The findings offer new insights into GTPase signaling, GTP hydrolysis, and nucleotide exchange mechanisms.
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