Extracting Orientation and Distance-Dependent Interaction Potentials between Proteins in Solutions Using Small-Angle X-ray/Neutron Scattering

Nonspecific protein-protein interactions (PPIs) are key to understanding the behavior of proteins in solutions. However, experimentally measuring anisotropic PPIs as a function of orientation and distance has been challenging. Here, we propose to measure a new parameter, the generalized second virial coefficient, <i>B</i><sub>22</sub>(<i>Q</i>), to address this challenge. <i>B</i><sub>22</sub>(<i>Q</i>) can be measured by using small-angle X-ray/neutron scattering (SAXS/SANS) at finite <i>Q</i> values, where <i>Q</i> is the magnitude of the scattering wave vector. We develop the analytical theory here to calculate <i>B</i><sub>22</sub>(<i>Q</i>) with any known interprotein potentials including anisotropic interaction potentials. This method overcomes the challenges and limitations of commonly used methods for extracting PPI information, namely, using integral approximations to solve the Ornstein-Zernike equation by fitting SAXS/SANS data. The accuracy of this analytical theory is further evaluated with computer simulations using a model system. Not only can our method greatly extend the capability of SAXS/SANS to investigate PPIs of many proteins, but it is also applicable to a wide variety of colloidal systems where anisotropic interaction potentials are important.

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Publication Details

Journal
The Journal of Physical Chemistry Letters
Published
2024-12-10
DOI
https://doi.org/10.1021/acs.jpclett.4c02629
Citations
2
Primary Topic
Protein Structure and Dynamics
Type
article
Field-Weighted Citation Impact
0.47

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article

Extracting Orientation and Distance-Dependent Interaction Potentials between Proteins in Solutions Using Small-Angle X-ray/Neutron Scattering

Harold W. Hatch, Alexander Grishaev, Marco A. Blanco, Guangcui Yuan et al.
2 citations
The Journal of Physical Chemistry Letters
Protein Structure and Dynamics
0.47
article

Extracting Orientation and Distance-Dependent Interaction Potentials between Proteins in Solutions Using Small-Angle X-ray/Neutron Scattering

Harold W. Hatch, Alexander Grishaev, Marco A. Blanco, Guangcui Yuan, Jainik Panchal, Yun Liu, Vincent K. Shen
article en
2 citations

Abstract

Nonspecific protein-protein interactions (PPIs) are key to understanding the behavior of proteins in solutions. However, experimentally measuring anisotropic PPIs as a function of orientation and distance has been challenging. Here, we propose to measure a new parameter, the generalized second virial coefficient, <i>B</i><sub>22</sub>(<i>Q</i>), to address this challenge. <i>B</i><sub>22</sub>(<i>Q</i>) can be measured by using small-angle X-ray/neutron scattering (SAXS/SANS) at finite <i>Q</i> values, where <i>Q</i> is the magnitude of the scattering wave vector. We develop the analytical theory here to calculate <i>B</i><sub>22</sub>(<i>Q</i>) with any known interprotein potentials including anisotropic interaction potentials. This method overcomes the challenges and limitations of commonly used methods for extracting PPI information, namely, using integral approximations to solve the Ornstein-Zernike equation by fitting SAXS/SANS data. The accuracy of this analytical theory is further evaluated with computer simulations using a model system. Not only can our method greatly extend the capability of SAXS/SANS to investigate PPIs of many proteins, but it is also applicable to a wide variety of colloidal systems where anisotropic interaction potentials are important.

The Journal of Physical Chemistry LettersVol. 15(50)
Merck & Co., Inc., Rahway, NJ, USA (United States) (US), National Institute of Standards and Technology (US), United States Military Academy (US), Material Measurement Laboratory (US), NIST Center for Neutron Research (US), University of Delaware (US)
National Institute of Standards and Technology, Division of Materials Research
Openalex Percentile: Top 34%
Protein Structure and Dynamics
0.47
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