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用于仿生纺丝制备韧性等同于蜘蛛拖牵丝的纤维的工程化蜘蛛丝蛋白

Engineered Spider Silk Proteins for Biomimetic Spinning of Fibers with Toughness Equal to Dragline Silks.

作者信息

Arndt Tina, Greco Gabriele, Schmuck Benjamin, Bunz Jessica, Shilkova Olga, Francis Juanita, Pugno Nicola M, Jaudzems Kristaps, Barth Andreas, Johansson Jan, Rising Anna

机构信息

Department of Biosciences and Nutrition Karolinska Institutet Neo Huddinge 14183 Sweden.

Laboratory for Bioinspired, Bionic, Nano, Meta, Materials & Mechanics Department of Civil, Environmental and Mechanical Engineering University of Trento Via Mesiano 77 Trento 38123 Italy.

出版信息

Adv Funct Mater. 2022 Jun 3;32(23):2200986. doi: 10.1002/adfm.202200986. Epub 2022 Mar 25.

DOI:10.1002/adfm.202200986
PMID:36505976
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9720699/
Abstract

Spider silk is the toughest fiber found in nature, and bulk production of artificial spider silk that matches its mechanical properties remains elusive. Development of miniature spider silk proteins (mini-spidroins) has made large-scale fiber production economically feasible, but the fibers' mechanical properties are inferior to native silk. The spider silk fiber's tensile strength is conferred by poly-alanine stretches that are zipped together by tight side chain packing in β-sheet crystals. Spidroins are secreted so they must be void of long stretches of hydrophobic residues, since such segments get inserted into the endoplasmic reticulum membrane. At the same time, hydrophobic residues have high β-strand propensity and can mediate tight inter-β-sheet interactions, features that are attractive for generation of strong artificial silks. Protein production in prokaryotes can circumvent biological laws that spiders, being eukaryotic organisms, must obey, and the authors thus design mini-spidroins that are predicted to more avidly form stronger β-sheets than the wildtype protein. Biomimetic spinning of the engineered mini-spidroins indeed results in fibers with increased tensile strength and two fiber types display toughness equal to native dragline silks. Bioreactor expression and purification result in a protein yield of ≈9 g L which is in line with requirements for economically feasible bulk scale production.

摘要

蜘蛛丝是自然界中发现的最坚韧的纤维,而大量生产具有与其机械性能相匹配的人造蜘蛛丝仍然难以实现。微型蜘蛛丝蛋白(迷你蜘蛛丝蛋白)的开发使大规模纤维生产在经济上可行,但这些纤维的机械性能不如天然蜘蛛丝。蜘蛛丝纤维的拉伸强度由聚丙氨酸链段赋予,这些链段在β-折叠晶体中通过紧密的侧链堆积而结合在一起。蜘蛛丝蛋白是分泌型的,因此它们必须没有长段的疏水残基,因为这些片段会插入内质网的膜中。与此同时,疏水残基具有较高的β-链倾向,并且可以介导紧密的β-折叠片层间相互作用,这些特性对于生产高强度的人造丝很有吸引力。原核生物中的蛋白质生产可以规避蜘蛛作为真核生物必须遵守的生物学规律,因此作者设计了迷你蜘蛛丝蛋白,预计它们比野生型蛋白更易于形成更强的β-折叠片层。对工程化迷你蜘蛛丝蛋白进行仿生纺丝确实能得到拉伸强度更高的纤维,并且两种纤维类型的韧性与天然牵引丝相当。生物反应器表达和纯化的蛋白产量约为9 g/L,这符合经济可行的大规模生产要求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc8f/9720699/e68cfe7b3fcf/ADFM-32-2200986-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc8f/9720699/bc1a98d5f66b/ADFM-32-2200986-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc8f/9720699/6d9a0e323f29/ADFM-32-2200986-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc8f/9720699/214c5892c72e/ADFM-32-2200986-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc8f/9720699/35a74a6256e3/ADFM-32-2200986-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc8f/9720699/d6271ff50973/ADFM-32-2200986-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc8f/9720699/e68cfe7b3fcf/ADFM-32-2200986-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc8f/9720699/bc1a98d5f66b/ADFM-32-2200986-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc8f/9720699/6d9a0e323f29/ADFM-32-2200986-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc8f/9720699/214c5892c72e/ADFM-32-2200986-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc8f/9720699/35a74a6256e3/ADFM-32-2200986-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc8f/9720699/d6271ff50973/ADFM-32-2200986-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc8f/9720699/e68cfe7b3fcf/ADFM-32-2200986-g006.jpg

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