Effect of pH and Copper(II) on the Conformation Transitions of Silk Fibroin Based on EPR, NMR, and Raman Spectroscopy†

Biochemistry ◽  
2004 ◽  
Vol 43 (38) ◽  
pp. 11932-11941 ◽  
Author(s):  
Xiao-Hong Zong ◽  
Ping Zhou ◽  
Zheng-Zhong Shao ◽  
Shi-Ming Chen ◽  
Xin Chen ◽  
...  
2010 ◽  
Vol 11 (7) ◽  
pp. 1796-1801 ◽  
Author(s):  
Qinqin Dang ◽  
Shoudong Lu ◽  
Shen Yu ◽  
Pingchuan Sun ◽  
Zhi Yuan

RSC Advances ◽  
2019 ◽  
Vol 9 (71) ◽  
pp. 41720-41728
Author(s):  
Shuai Zhang ◽  
Minghan Han

The effect of pH on polynuclear molybdenum species (isopolymolybdates) synthesis was investigated by Raman spectroscopy.


1989 ◽  
Vol 43 (7) ◽  
pp. 1269-1272 ◽  
Author(s):  
Siding Zheng ◽  
Guanxian Li ◽  
Wenhuo Yao ◽  
Tongyin Yu

The mechanical denaturation process of silk fibroin is examined by Raman spectroscopy. The fresh silk fibroins from the middle gland of mature silkworms are drawn to various ratios on a tensile tester ( R = ldrawn/ linitial, where l is length) and their conformations are measured with Raman spectroscopy. Undrawn silk fibroin is mainly in the random coil structure with some α-helical conformation, the characteristic bands appearing at 1252 and 1660 (random coil) and at 942, 1106, and 1270 cm−1 (α-helix). When the samples are drawn up to R = 4 at an extension rate of 500 mm/min, two peaks at 1233 cm−1 (the amide III band) and 1085 cm−1 appear; it is shown that the β-sheet conformation is then formed. With an increase in drawing ratios, the intensities of these β-sheet bands increase and those of the random coil and α-helical bands decrease gradually. These changes indicate that, under the action of stress, the conformation of fibroin is altered from random coil and α-helix to β-sheet structures. This result is quite similar to the results achieved by the spinning of the silkworm. The effect of the water content in liquid silk on this conformational transition process is revealed and discussed.


Polymers ◽  
2019 ◽  
Vol 11 (10) ◽  
pp. 1622 ◽  
Author(s):  
Xin Zhang ◽  
Zhijuan Pan

With excellent biocompatibility and biodegradability, silk fibroin has been developed into many protein materials. For producing regenerated silk fibroin (RSF) fibers, the conformation transition of silk fibroin needs to be thoroughly studied during the spinning process. Since the many silk fabrics that are discarded comprise an increasing waste of resources and increase the pressure on the environment, in this paper, waste silk fiber was recycled in an attempt to prepare regenerated fibroin fiber by dry-wet spinning. Ethanol was the coagulation bath. The rheological properties of all the RSF solutions were investigated to acquire rheology curves and non-Newtonian indexes for spinnability analysis. Four stages of the spinning process were carried out to obtain RSF samples and study their conformation transitions, crystallization, and thermal properties by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction, and differential scanning calorimetry. Quantitative analysis of the FTIR results was performed to obtain specific data regarding the contents of the secondary structures. The results showed that higher concentration spinning solutions had better spinnability. As the spinning process progressed, random coils were gradually converted into β-sheets and crystallization increased. Among the different influencing factors, the ethanol coagulation bath played a leading role in the conformation transitions of silk fibroin.


1992 ◽  
Vol 48 (3) ◽  
pp. 141-144 ◽  
Author(s):  
Zuglul Haider Ayub ◽  
Kiyoshi Hirabayashi ◽  
Mitsuo Arai
Keyword(s):  

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