TY - JOUR
T1 - Mobility Capillary Electrophoresis-Restrained Modeling Method for Protein Structure Analysis in Mixtures
AU - Zhang, Rongkai
AU - Wu, Haimei
AU - He, Muyi
AU - Zhang, Wenjing
AU - Xu, Wei
N1 - Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/3/14
Y1 - 2019/3/14
N2 - Protein stereostructure analysis in mixtures still remains challenging, especially large-scale analysis such as in proteomics. With the capability of measuring the hydrodynamic radius of ions in the liquid phase, mobility capillary electrophoresis (MCE) has been applied to study the structure of peptides. In this study, MCE was extended for protein mixture separation and their corresponding hydrodynamic radius analyses. After ellipsoid approximation, the results obtained by MCE experiments were then used as a restraint in molecular dynamics simulations to predict the most probable structure of each protein. Besides a three-protein mixture, a mixture of disulfide bond reduced insulin was also studied by this MCE-restrained modeling method. The results obtained by this method agree with literature studies, and mass spectrometry experiments were also carried out to confirm our findings.
AB - Protein stereostructure analysis in mixtures still remains challenging, especially large-scale analysis such as in proteomics. With the capability of measuring the hydrodynamic radius of ions in the liquid phase, mobility capillary electrophoresis (MCE) has been applied to study the structure of peptides. In this study, MCE was extended for protein mixture separation and their corresponding hydrodynamic radius analyses. After ellipsoid approximation, the results obtained by MCE experiments were then used as a restraint in molecular dynamics simulations to predict the most probable structure of each protein. Besides a three-protein mixture, a mixture of disulfide bond reduced insulin was also studied by this MCE-restrained modeling method. The results obtained by this method agree with literature studies, and mass spectrometry experiments were also carried out to confirm our findings.
UR - http://www.scopus.com/inward/record.url?scp=85062881736&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcb.9b01148
DO - 10.1021/acs.jpcb.9b01148
M3 - Article
C2 - 30807169
AN - SCOPUS:85062881736
SN - 1520-6106
VL - 123
SP - 2335
EP - 2341
JO - Journal of Physical Chemistry B
JF - Journal of Physical Chemistry B
IS - 10
ER -