Real-Time Monitoring of the Structural Transition of Bombyx mori Liquid Silk under Pressure by Solid-State NMR

被引:6
作者
Suzuki, Yu [1 ]
Morie, Shota [1 ]
Okamura, Hideyasu [1 ]
Asakura, Tetsuo [2 ]
Naito, Akira [2 ,3 ]
机构
[1] Univ Fukui, Grad Sch Engn, Dept Appl Chem & Biotechnol, Fukui, Fukui 9108507, Japan
[2] Tokyo Univ Agr & Technol, Dept Biotechnol, Tokyo 1848588, Japan
[3] Yokohama Natl Univ, Grad Sch Engn, Yokohama 2408501, Japan
关键词
BETA-TURN STRUCTURE; SPINNING APPARATUS; LAMELLAR STRUCTURE; AQUEOUS-SOLUTION; FIBROIN SOLUTION; MIDDLE DIVISION; FLOW-ANALYSIS; MODEL; CHAIN; BACTERIORHODOPSIN;
D O I
10.1021/jacs.3c04361
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Silk fibroin is stored in the silk glands of Bombyx mori silkworms as a condensed aqueous solution called liquid silk. It is converted into silk fibers at the silkworm's spinnerets under mechanical forces including shear stress and pressure. However, the detailed mechanism of the structural transition of liquid silk to silk fibers under pressure is not well understood. Magic angle spinning (MAS) in solid-state nuclear magnetic resonance (NMR) can exert pressure on liquid samples in a quantitative manner. In this study, solid-state NMR was used to quantitatively analyze the impact of pressure on the structural transition of liquid silk. A combination of C-13 DD-MAS and CP-MAS NMR measurements enabled the conformation and dynamics of the crystalline region of the silk fibroin (both before (Silk I-p) and after (Silk IIp) the structural transition) to be detected in real time with atomic resolution. Spectral analyses proposed that the pressure-induced structural transition from Silk I-p to Silk IIp proceeds by a two-step autocatalytic reaction mechanism. The first reaction step is a nucleation step in which Silk I-p transforms to single lamellar Silk IIp, and the second is a growth step in which the single lamellar Silk IIp acts as a catalyst that reacts with Silk I-p molecules to further form Silk IIp molecules, resulting in stacked lamellar Silk IIp. Furthermore, the rate constant in the second step shows a significant pressure dependence, with an increase in pressure accelerating the formation of large stacked lamellar Silk IIp.
引用
收藏
页码:22925 / 22933
页数:9
相关论文
共 48 条
[1]   Proteins in Wonderland: The Magical World of Pressure [J].
Akasaka, Kazuyuki ;
Maeno, Akihiro .
BIOLOGY-BASEL, 2022, 11 (01)
[2]   Silk Spinning in Silkworms and Spiders [J].
Andersson, Marlene ;
Johansson, Jan ;
Rising, Anna .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2016, 17 (08)
[3]   Refinement of repeated β-turn structure for silk I conformation of Bombyx mori silk fibroin using 13C solid-state NMR and X-ray diffraction methods [J].
Asakura, T ;
Ohgo, K ;
Komatsu, K ;
Kanenari, M ;
Okuyama, K .
MACROMOLECULES, 2005, 38 (17) :7397-7403
[4]   A repeated β-turn structure in poly(Ala-Gly) as a model for silk I of Bombyx mori silk fibroin studied with two-dimensional spin-diffusion NMR under off magic angle spinning and rotational echo double resonance [J].
Asakura, T ;
Ashida, J ;
Yamane, T ;
Kameda, T ;
Nakazawa, Y ;
Ohgo, K ;
Komatsu, K .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 306 (02) :291-305
[5]   Lamellar structure in Poly(Ala-Gly) determined by solid-state NMR and statistical mechanical calculations [J].
Asakura, Tetsuo ;
Sato, Hirohiko ;
Moro, Fumika ;
Nakazawa, Yasumoto ;
Aoki, Akihiro .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (17) :5703-5709
[6]   Some observations on the structure and function of the spinning apparatus in the silkworm Bombyx mori [J].
Asakura, Tetsuo ;
Umemura, Kosuke ;
Nakazawa, Yasumoto ;
Hirose, Haruko ;
Higham, James ;
Knight, David .
BIOMACROMOLECULES, 2007, 8 (01) :175-181
[7]   Structure of silk I (Bombyx mori silk fibroin before spinning) in the dry and hydrated states studied using 13C solid-state NMR spectroscopy [J].
Asakura, Tetsuo ;
Naito, Akira .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2022, 216 :282-290
[8]   Structure of Silk I (Bombyx mori Silk Fibroin before Spinning) -Type II β-Turn, Not α-Helix- [J].
Asakura, Tetsuo .
MOLECULES, 2021, 26 (12)
[9]   Chain-folded lamellar structure and dynamics of the crystalline fraction of Bombyx mori silk fibroin and of (Ala-Gly-Ser-Gly-Ala-Gly)n model peptides [J].
Asakura, Tetsuo ;
Ogawa, Tatsuya ;
Naito, Akira ;
Williamson, Michael P. .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2020, 164 :3974-3983
[10]   Lamellar Structure in Alanine-Glycine Copolypeptides Studied by Solid-State NMR Spectroscopy: A Model for the Crystalline Domain of Bombyx mori Silk Fibroin in Silk II Form [J].
Asakura, Tetsuo ;
Aoki, Akihiro ;
Komatsu, Kohei ;
Ito, Chie ;
Suzuki, Ikue ;
Naito, Akira ;
Kaji, Hironori .
BIOMACROMOLECULES, 2020, 21 (08) :3102-3111