Interaction of Extracellular Loop II of κ-Opioid Receptor (196–228) with Opioid Peptide Dynorphin in Membrane Environments as Revealed by Solid State Nuclear Magnetic Resonance, Quartz Crystal Microbalance and Molecular Dynamics Simulation

2014 ◽  
Vol 118 (32) ◽  
pp. 9604-9612 ◽  
Author(s):  
Atsushi Kira ◽  
Namsrai Javkhlantugs ◽  
Takenori Miyamori ◽  
Yoshiyuki Sasaki ◽  
Masayuki Eguchi ◽  
...  
2021 ◽  
Vol 16 (4) ◽  
pp. 041003
Author(s):  
Mahsa Moradipour ◽  
Xinjie Tong ◽  
Brian Novak ◽  
Poorya Kamali ◽  
Shardrack O. Asare ◽  
...  

Molecules ◽  
2020 ◽  
Vol 25 (11) ◽  
pp. 2634
Author(s):  
Tetsuo Asakura

This review will introduce very recent studies using solid-state nuclear magnetic resonance (NMR) and molecular dynamics (MD) simulation on the structure and dynamics of spider dragline silks conducted by the author’s research group. Spider dragline silks possess extraordinary mechanical properties by combining high tensile strength with outstanding elongation before breaking, and therefore continue to attract attention of researchers in biology, biochemistry, biophysics, analytical chemistry, polymer technology, textile technology, and tissue engineering. However, the inherently non-crystalline structure means that X-ray diffraction and electron diffraction methods provide only limited information because it is difficult to study the molecular structure of the amorphous region. The most detailed picture of the structure and dynamics of the silks in the solid state experimentally have come from solid-state NMR measurements coupled with stable isotope labeling of the silks and the related silk peptides. In addition, combination of solid-state NMR and MD simulation was very powerful analytical tools to understand the local conformation and dynamics of the spider dragline silk in atomic resolution. In this review, the author will emphasize how solid-state NMR and MD simulation have contributed to a better understanding of the structure and dynamics in the spider dragline silks.


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