Raman Spectroscopic Evidence for Side-Chain Unfolding in Spider Dragline Silk under Tensile Deformation

2005 ◽  
Vol 874 ◽  
Author(s):  
Xiaojun He ◽  
Michael S. Ellison ◽  
Jacqueline M. Palmer

AbstractIn-situ Ramanspectra were collected on the N. clavipes spider dragline silk under a tensile deformation rate of 15mm/min. The most prominent features on the spectra were due to those bands near 1100 cm-1, which present as a sensitive probe to structural changes associated with side-chains of silk peptide. A downshift of Raman bands at 1095 cm-1 and 1089 cm-1 was detected with increasing strain. Furthermore, an increase in the intensity of the Raman band at 1062 cm-1 due to the vibration of trans structure without lateral coupling was prominent at certain strain levels. This was interpreted in terms of a morphology transition from the random configuration to the trans conformation modulated by the reorganization of the hydrogen bonding among the side-chain.

2014 ◽  
Vol 6 (19) ◽  
pp. 16827-16834 ◽  
Author(s):  
Seung-Mo Lee ◽  
Eckhard Pippel ◽  
Oussama Moutanabbir ◽  
Jae-Hyun Kim ◽  
Hak-Joo Lee ◽  
...  

2020 ◽  
Vol 21 (12) ◽  
pp. 5306-5314
Author(s):  
Linli Hu ◽  
Qianying Chen ◽  
Jinrong Yao ◽  
Zhengzhong Shao ◽  
Xin Chen

2014 ◽  
Vol 50 (37) ◽  
pp. 4856-4859 ◽  
Author(s):  
Xiangyan Shi ◽  
Jeffery L. Yarger ◽  
Gregory P. Holland

2H–13C HETCOR MAS NMR is performed on 2H/13C/15N-Pro enriched A. aurantia dragline silk. Proline dynamics are extracted from 2H NMR line shapes and T1 in a site-specific manner to elucidate the backbone and side chain molecular dynamics for the MaSp2 GPGXX β-turn regions for spider dragline silk in the dry and wet, supercontracted states.


2008 ◽  
Vol 41 (2) ◽  
pp. 390-398 ◽  
Author(s):  
Anja Glišović ◽  
Thorsten Vehoff ◽  
Richard J. Davies ◽  
Tim Salditt

Evolution ◽  
2006 ◽  
Vol 60 (12) ◽  
pp. 2539 ◽  
Author(s):  
Brook O. Swanson ◽  
Todd A. Blackledge ◽  
Adam P. Summers ◽  
Cheryl Y. Hayashi

Author(s):  
Lizhong Dong ◽  
Jian Qiao ◽  
Yulong Wu ◽  
Ming Ren ◽  
Yulian Wang ◽  
...  

2010 ◽  
Vol 5 (9) ◽  
pp. 1934578X1000500
Author(s):  
Iris Stappen ◽  
Joris Höfinghoff ◽  
Gerhard Buchbauer ◽  
Peter Wolschann

Structural modifications of natural (-)-( Z)-β-santalol have shown that the sandalwood odor impression is highly sensitive, even to small structural changes. Particularly, the substitution of the quaternary carbon is of great influence on the scent. Epi-compounds with side chains in the endo-position possess sandalwood odor in only a few derivatives, whereas modifications at this side chain, as well as modification at the bicyclic ring systems mostly lead to a complete loss of sandalwood fragrance.


2020 ◽  
Author(s):  
Sachin Kumar ◽  
Yujen Wang ◽  
Manuel K. Rausch ◽  
Sapun H. Parekh

AbstractFibrin is a fibrous protein network that entraps blood cells and platelets to form blood clots following vascular injury. As a biomaterial, fibrin acts a biochemical scaffold as well as a viscoelastic patch that resists mechanical insults. The biomechanics and biochemistry of fibrin have been well characterized independently, showing that fibrin is a hierarchical material with numerous binding partners. However, comparatively little is known about how fibrin biomechanics and biochemistry are coupled: how does fibrin deformation influence its biochemistry at the molecular level? In this study, we show how mechanically-induced molecular structural changes in fibrin affect fibrin biochemistry and fibrin-platelet interaction. We found that tensile deformation of fibrin lead to molecular structural transitions of α-helices to β-sheets, which reduced binding of tissue plasminogen activator (tPA), an enzyme that initiates fibrinolysis, at the network and single fiber level. Moreover, binding of tPA and Thioflavin T (ThT), a commonly used β-sheet marker, was primarily mutually exclusive such that tPA bound to native (helical) fibrin whereas ThT bound to strained fibrin. Finally, we demonstrate that conformational changes in fibrin suppressed the biological activity of platelets on mechanically strained fibrin due to attenuated αIIbβ3 integrin binding. Our work shows that mechanical strain regulates fibrin molecular structure and fibrin biological activity in an elegant mechano-chemical feedback loop, which likely influences fibrinolysis and wound healing kinetics.


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