Methods of generating highly-crystalline recombinant spider silk protein fibers

US12209331B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12209331-B2
Application numberUS-202117527617-A
CountryUS
Kind codeB2
Filing dateNov 16, 2021
Priority dateSep 25, 2017
Publication dateJan 28, 2025
Grant dateJan 28, 2025

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Provided herein are scalable methods of processing wet-spun fiber comprising recombinant spider silk polypeptides to generate a three-dimensional crystalline lattice of beta-sheet structures in the fiber.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method for generating a drawn fiber comprising a silk polypeptide, the method comprising: dissolving a powder comprising the silk polypeptide into a solvent to generate a spin dope; extruding the spin dope into a coagulation bath to form a precursor fiber; collecting the precursor fiber without drawing the precursor fiber; annealing the precursor fiber prior to drawing the fiber; and drawing the precursor fiber only over a surface having a temperature of at least 190° C. to generate a drawn fiber, wherein the drawn fiber has a crystallinity index of at least 6% as measured using X-ray diffraction. 2. The method of claim 1 , wherein said silk polypeptide is a recombinant silk polypeptide. 3. The method of claim 2 , wherein said recombinant silk polypeptide comprises two or more repeat units of a proteinaceous block copolymer. 4. The method of claim 1 , wherein said silk polypeptide is a recombinant spider silk polypeptide. 5. The method of claim 4 , wherein the recombinant spider silk polypeptide comprises SEQ ID NO: 1. 6. The method of claim 1 , wherein the powder comprising the silk polypeptide is comprised of at least 60% silk polypeptide by weight. 7. The method of claim 1 , wherein the drawn fiber is drawn over the surface at a draw ratio of at least 2×. 8. The method of claim 7 , wherein the draw ratio is computed by determining the draw ratio at failure. 9. The method of claim 8 , wherein determining the draw ratio at failure comprises determining the distribution of maximum elongation at break of one or more precursor fibers using an apparatus designed to draw the fiber over a surface having a temperature of at least 190° C. while increasing the draw ratio. 10. The method of claim 1 , further comprising drawing the drawn fiber over the surface having a temperature of at least 190° C. one or more times. 11. The method of claim 10 , wherein the sum of the draw ratios at each drawing step is approximately equal to or less than the draw ratio at failure of the precursor fiber. 12. The method of claim 10 , wherein the generation of the drawn fiber comprises: determining a draw ratio at failure of the precursor fiber; and distributing the draw ratio at failure of the precursor fiber over each of said drawing steps. 13. The method of claim 1 , wherein annealing the precursor fiber comprises annealing the precursor fiber with alcohol vapor. 14. The method of claim 1 , wherein the solvent comprises N-methyl morpholine N-oxide (NMMO) or formic acid. 15. The method of claim 14 , wherein the solvent comprises 20% to 60% by weight NMMO. 16. The method of claim 14 , wherein generating said drawn fiber comprises heating said spin dope before said step of extruding the spin dope into said coagulation bath. 17. The method of claim 14 , wherein extruding the spin dope into said coagulation bath comprises extruding the spin dope through an air in the range of 2 to 20 cm. 18. The method of claim 1 , wherein the drawn fiber has increased beta-sheet formation relative to the precursor fiber. 19. The method of claim 18 , wherein the drawn fiber has increased beta-sheet formation relative to the precursor fiber proportional to the draw ratio used to draw the fiber over the surface. 20. The method of claim 1 , wherein the surface is at least 200 degrees Celsius. 21. The method of claim 1 , wherein the surface is at least 20 degrees Celsius greater than the glass transition temperature of the precursor fiber. 22. The method of claim 1 , wherein the tenacity of the drawn fiber is greater than 20 cN/tex. 23. The method of claim 1 , wherein the Herman orientation factor of the drawn fiber is approximately the same as native silk fiber. 24. The method of claim 1 , wherein the drawn fiber has a crystallinity index of at least 7% as measured using X-ray diffraction. 25. The method of claim 1 , wherein the drawn fiber has more than 1.5 times increased beta-sheet content as compared to air drawn fibers subject to identical drawing conditions except not drawn over a surface having a temperature of at least 190° C. 26. The method of claim 1 , wherein the drawn fiber has an increased 3D β-sheet content as compared to air drawn fibers subject to identical drawing conditions except not drawn over a surface having a temperature of at least 190° C. 27. The method of claim 1 , further comprising drying the precursor fiber after the collecting and before the annealing to form a dried precursor fiber, wherein the drawing comprises drawing the dried precursor fiber only over the surface to generate the drawn fiber.

Assignees

Inventors

Classifications

  • by contact with at least one rotating roll · CPC title

  • from polyaminoacids or polypeptides · CPC title

  • from fibroin · CPC title

  • Preparation of spinning solutions · CPC title

  • D02J1/221Primary

    Preliminary treatments · CPC title

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Frequently asked questions

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What does patent US12209331B2 cover?
Provided herein are scalable methods of processing wet-spun fiber comprising recombinant spider silk polypeptides to generate a three-dimensional crystalline lattice of beta-sheet structures in the fiber.
Who is the assignee on this patent?
Bolt Threads Inc
What technology area does this patent fall under?
Primary CPC classification D02J1/221. Mapped technology areas include Textiles & Paper.
When was this patent published?
Publication date Tue Jan 28 2025 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 4 related publications on this page (citations in our corpus or others sharing the same primary CPC).