Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Article
  • Published:

Self-assembly of peptide nanocapsules by a solvent concentration gradient

Abstract

Biological systems can create materials with intricate structures and specialized functions. In comparison, precise control of structures in human-made materials has been challenging. Here we report on insect cuticle peptides that spontaneously form nanocapsules through a single-step solvent exchange process, where the concentration gradient resulting from the mixing of water and acetone drives the localization and self-assembly of the peptides into hollow nanocapsules. The underlying driving force is found to be the intrinsic affinity of the peptides for a particular solvent concentration, while the diffusion of water and acetone creates a gradient interface that triggers peptide localization and self-assembly. This gradient-mediated self-assembly offers a transformative pathway towards simple generation of drug delivery systems based on peptide nanocapsules.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Fig. 1: De novo sequencing and screening of nanocapsule-forming peptides from O. furnacalis.
Fig. 2: The assembly of ICPs in water–acetone mixed solvent.
Fig. 3: Transition of ICP secondary structure during the self-assembly process.
Fig. 4: Exploring the driving forces of ICP self-assembly through MD simulations.
Fig. 5: Encapsulating protein and drug by ICP capsules.
Fig. 6: Intracellular drug, protein and mRNA delivery into cells using ICPs nanocapsules.

Similar content being viewed by others

Data availability

The data that support the plots within this paper and other findings of this study are available via DR-NTU at https://doi.org/10.21979/N9/DJV2BM (ref. 58). The data that support the findings of this study are also available from the corresponding authors upon reasonable request. Source data are provided with this paper.

Code availability

All code and scripts used in this study are available from the corresponding authors upon reasonable request.

References

  1. Bar-Cohen, Y. Biomimetics—using nature to inspire human innovation. Bioinspir. Biomim. 1, P1 (2006).

    Article  PubMed  Google Scholar 

  2. Liu, Z., Meyers, M. A., Zhang, Z. & Ritchie, R. O. Functional gradients and heterogeneities in biological materials: design principles, functions, and bioinspired applications. Prog. Mater. Sci. 88, 467–498 (2017).

    Article  CAS  Google Scholar 

  3. Waite, J. H., Lichtenegger, H. C., Stucky, G. D. & Hansma, P. Exploring molecular and mechanical gradients in structural bioscaffolds. Biochemistry 43, 7653–7662 (2004).

    Article  CAS  PubMed  Google Scholar 

  4. Miserez, A., Li, Y., Waite, J. H. & Zok, F. Jumbo squid beaks: inspiration for design of robust organic composites. Acta Biomater. 3, 139–149 (2007).

    Article  CAS  PubMed  Google Scholar 

  5. Ho, S. P., Marshall, S. J., Ryder, M. I. & Marshall, G. W. The tooth attachment mechanism defined by structure, chemical composition and mechanical properties of collagen fibers in the periodontium. Biomaterials 28, 5238–5245 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Meyers, M. A., McKittrick, J. & Chen, P.-Y. Structural biological materials: critical mechanics–materials connections. Science 339, 773–779 (2013).

    Article  CAS  PubMed  Google Scholar 

  7. Fratzl, P. & Weinkamer, R. Nature’s hierarchical materials. Prog. Mater. Sci. 52, 1263–1334 (2007).

    Article  CAS  Google Scholar 

  8. Heinemann, F., Launspach, M., Gries, K. & Fritz, M. Gastropod nacre: structure, properties and growth—biological, chemical and physical basics. Biophys. Chem. 153, 126–153 (2011).

    Article  CAS  PubMed  Google Scholar 

  9. Chen, P.-Y., Stokes, A. & McKittrick, J. Comparison of the structure and mechanical properties of bovine femur bone and antler of the North American elk (Cervus elaphus canadensis). Acta Biomater. 5, 693–706 (2009).

    Article  PubMed  Google Scholar 

  10. Silva, E. C. N., Walters, M. C. & Paulino, G. H. Modeling bamboo as a functionally graded material: lessons for the analysis of affordable materials. J. Mater. Sci. 41, 6991–7004 (2006).

    Article  CAS  Google Scholar 

  11. Korevaar, P. A., Schaefer, C., de Greef, T. F. & Meijer, E. Controlling chemical self-assembly by solvent-dependent dynamics. J. Am. Chem. Soc. 134, 13482–13491 (2012).

    Article  CAS  PubMed  Google Scholar 

  12. Wang, J. et al. Trace solvent as a predominant factor to tune dipeptide self-assembly. ACS Nano 10, 2138–2143 (2016).

    Article  CAS  PubMed  Google Scholar 

  13. Hartgerink, J. D., Beniash, E. & Stupp, S. I. Self-assembly and mineralization of peptide-amphiphile nanofibers. Science 294, 1684–1688 (2001).

    Article  CAS  PubMed  Google Scholar 

  14. Lee, B. K., Yun, Y. & Park, K. PLA micro- and nano-particles. Adv. Drug Deliv. Rev. 107, 176–191 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. El-Sheikh, S., El-Sherbiny, S., Barhoum, A. & Deng, Y. Effects of cationic surfactant during the precipitation of calcium carbonate nano-particles on their size, morphology, and other characteristics. Colloids Surf. A 422, 44–49 (2013).

    Article  CAS  Google Scholar 

  16. Cheng, J. et al. Formulation of functionalized PLGA–PEG nanoparticles for in vivo targeted drug delivery. Biomaterials 28, 869–876 (2007).

    Article  CAS  PubMed  Google Scholar 

  17. Moreno‐Alcántar, G. et al. Solvent‐driven supramolecular wrapping of self‐assembled structures. Angew. Chem. Int. Ed. Engl. 133, 5467–5473 (2021).

    Article  Google Scholar 

  18. Te Brinke, E. et al. Dissipative adaptation in driven self-assembly leading to self-dividing fibrils. Nat. Nanotechnol. 13, 849–855 (2018).

    Article  Google Scholar 

  19. Albert, J. N. & Epps, T. H. III Self-assembly of block copolymer thin films. Mater. Today 13, 24–33 (2010).

    Article  CAS  Google Scholar 

  20. Knowles, T. P., Oppenheim, T. W., Buell, A. K., Chirgadze, D. Y. & Welland, M. E. Nanostructured films from hierarchical self-assembly of amyloidogenic proteins. Nat. Nanotechnol. 5, 204–207 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Rideau, E., Wurm, F. R. & Landfester, K. Self‐assembly of giant unilamellar vesicles by film hydration methodologies. Adv. Biosyst. 3, 1800324 (2019).

    Article  Google Scholar 

  22. Blanazs, A., Armes, S. P. & Ryan, A. J. Self‐assembled block copolymer aggregates: from micelles to vesicles and their biological applications. Macromol. Rapid Commun. 30, 267–277 (2009).

    Article  CAS  PubMed  Google Scholar 

  23. Cui, H., Chen, Z., Zhong, S., Wooley, K. L. & Pochan, D. J. Block copolymer assembly via kinetic control. Science 317, 647–650 (2007).

    Article  CAS  PubMed  Google Scholar 

  24. Rabani, E., Reichman, D. R., Geissler, P. L. & Brus, L. E. Drying-mediated self-assembly of nanoparticles. Nature 426, 271–274 (2003).

    Article  CAS  PubMed  Google Scholar 

  25. Sorrenti, A., Leira-Iglesias, J., Markvoort, A. J., de Greef, T. F. & Hermans, T. M. Non-equilibrium supramolecular polymerization. Chem. Soc. Rev. 46, 5476–5490 (2017).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Rivas, C. J. M. et al. Nanoprecipitation process: from encapsulation to drug delivery. Int. J. Pharm. 532, 66–81 (2017).

    Article  Google Scholar 

  27. Andersen, S. O. Biochemistry of insect cuticle. Annu. Rev. Entomol. 24, 29–59 (1979).

    Article  CAS  Google Scholar 

  28. Gopalan Nair, K. & Dufresne, A. Crab shell chitin whisker reinforced natural rubber nanocomposites. 1. Processing and swelling behavior. Biomacromolecules 4, 657–665 (2003).

    Article  PubMed  Google Scholar 

  29. Bogatyreva, N. S., Finkelstein, A. V. & Galzitskaya, O. V. Trend of amino acid composition of proteins of different taxa. J. Bioinform. Comput. Biol. 4, 597–608 (2006).

    Article  CAS  PubMed  Google Scholar 

  30. Willis, J. H. Structural cuticular proteins from arthropods: annotation, nomenclature, and sequence characteristics in the genomics era. Insect Biochem. Mol. Biol. 40, 189–204 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Kajava, A. V. Tandem repeats in proteins: from sequence to structure. J. Struct. Biol. 179, 279–288 (2012).

    Article  CAS  PubMed  Google Scholar 

  32. Lebouille, J., Stepanyan, R., Slot, J., Stuart, M. C. & Tuinier, R. Nanoprecipitation of polymers in a bad solvent. Colloids Surf. A 460, 225–235 (2014).

    Article  CAS  Google Scholar 

  33. Aryal, S., Hu, C.-M. J. & Zhang, L. Polymer–cisplatin conjugate nanoparticles for acid-responsive drug delivery. ACS Nano 4, 251–258 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. Hyde, C., Johnson, T. & Sheppard, R. Internal aggregation during solid phase peptide synthesis. Dimethyl sulfoxide as a powerful dissociating solvent. J. Chem. Soc. Chem. Commun. https://doi.org/10.1039/C39920001573 (1992).

  35. Srivastava, K. R., Kumar, A., Goyal, B. & Durani, S. Stereochemistry and solvent role in protein folding: nuclear magnetic resonance and molecular dynamics studies of poly-l and alternating-l, d homopolypeptides in dimethyl sulfoxide. J. Phys. Chem. B 115, 6700–6708 (2011).

    Article  CAS  PubMed  Google Scholar 

  36. Mendoza-Novelo, B., Mata-Mata, J. L., Vega-González, A., Cauich-Rodríguez, J. V. & Marcos-Fernández, Á. Synthesis and characterization of protected oligourethanes as crosslinkers of collagen-based scaffolds. J. Mater. Chem. B 2, 2874–2882 (2014).

    Article  CAS  PubMed  Google Scholar 

  37. Gu, L., Jiang, Y. & Hu, J. Scalable spider‐silk‐like supertough fibers using a pseudoprotein polymer. Adv. Mater. 31, 1904311 (2019).

    Article  CAS  Google Scholar 

  38. Annabi, N. et al. Synthesis of highly porous crosslinked elastin hydrogels and their interaction with fibroblasts in vitro. Biomaterials 30, 4550–4557 (2009).

    Article  CAS  PubMed  Google Scholar 

  39. Nowatzki, P. J. & Tirrell, D. A. Physical properties of artificial extracellular matrix protein films prepared by isocyanate crosslinking. Biomaterials 25, 1261–1267 (2004).

    Article  CAS  PubMed  Google Scholar 

  40. Ramos, R. et al. Nanocapsules produced by nanoprecipitation of designed suckerin-silk fusion proteins. ACS Macro Lett. 10, 628–634 (2021).

    Article  CAS  PubMed  Google Scholar 

  41. Zhang, L. et al. Microfluidic synthesis of rigid nanovesicles for hydrophilic reagents delivery. Angew. Chem. Int. Ed. Engl. 127, 4024–4028 (2015).

    Article  Google Scholar 

  42. Wang, Z., Rutjes, F. P. & van Hest, J. C. pH responsive polymersome Pickering emulsion for simple and efficient Janus polymersome fabrication. Chem. Commun. 50, 14550–14553 (2014).

    Article  CAS  Google Scholar 

  43. Reuvers, A. & Smolders, C. Formation of membranes by means of immersion precipitation: part II. The mechanism of formation of membranes prepared from the system cellulose acetate-acetone-water. J. Membr. Sci. 34, 67–86 (1987).

    Article  CAS  Google Scholar 

  44. Taylor, N. O., Wei, M.-T., Stone, H. A. & Brangwynne, C. P. Quantifying dynamics in phase-separated condensates using fluorescence recovery after photobleaching. Biophys. J. 117, 1285–1300 (2019).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  45. Ray, S. et al. Mass photometric detection and quantification of nanoscale α-synuclein phase separation. Nat. Chem. 15, 1306–1316 (2023).

    Article  CAS  PubMed  Google Scholar 

  46. Greenfield, N. J. Analysis of the kinetics of folding of proteins and peptides using circular dichroism. Nat. Protoc. 1, 2891–2899 (2006).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  47. Vögeli, B., Kazemi, S., Güntert, P. & Riek, R. Spatial elucidation of motion in proteins by ensemble-based structure calculation using exact NOEs. Nat. Struct. Mol. Biol. 19, 1053–1057 (2012).

    Article  PubMed  Google Scholar 

  48. Ulijn, R. V. & Smith, A. M. Designing peptide based nanomaterials. Chem. Soc. Rev. 37, 664–675 (2008).

    Article  CAS  PubMed  Google Scholar 

  49. Nauman, J. V., Campbell, P. G., Lanni, F. & Anderson, J. L. Diffusion of insulin-like growth factor-I and ribonuclease through fibrin gels. Biophys. J. 92, 4444–4450 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  50. Cui, H., Webber, M. J. & Stupp, S. I. Self‐assembly of peptide amphiphiles: from molecules to nanostructures to biomaterials. Biopolymers 94, 1–18 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  51. Tian, Y., Tirrell, M. V. & LaBelle, J. L. Harnessing the therapeutic potential of biomacromolecules through intracellular delivery of nucleic acids, peptides, and proteins. Adv. Healthc. Mater. 11, 2270066 (2022).

    Article  Google Scholar 

  52. Tang, L. et al. Investigating the optimal size of anticancer nanomedicine. Proc. Natl Acad. Sci. USA 111, 15344–15349 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  53. Midoux, P., Pichon, C., Yaouanc, J. J. & Jaffrès, P. A. Chemical vectors for gene delivery: a current review on polymers, peptides and lipids containing histidine or imidazole as nucleic acids carriers. Br. J. Pharmacol. 157, 166–178 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  54. Xiang, Z. et al. Adding an unnatural covalent bond to proteins through proximity-enhanced bioreactivity. Nat. Methods 10, 885–888 (2013).

    Article  CAS  PubMed  Google Scholar 

  55. Ruoslahti, E. & Pierschbacher, M. D. New perspectives in cell adhesion: RGD and integrins. Science 238, 491–497 (1987).

    Article  CAS  PubMed  Google Scholar 

  56. Naldini, L. Gene therapy returns to centre stage. Nature 526, 351–360 (2015).

    Article  CAS  PubMed  Google Scholar 

  57. Pardi, N. et al. Administration of nucleoside-modified mRNA encoding broadly neutralizing antibody protects humanized mice from HIV-1 challenge. Nat. Commun. 8, 14630 (2017).

    Article  PubMed  PubMed Central  Google Scholar 

  58. Haopeng, L. et al. Data for: harnessing gradients for self-assembly of peptide-based nanocapsules: a pathway to advanced drug delivery systems. DR-NTU (Data) https://doi.org/10.21979/N9/DJV2BM (2023).

Download references

Acknowledgements

H.L., X.H. and J.Y acknowledge support from the Singapore National Research Fellowship (NRF-NRFF11-2019-0004) and the Singapore Ministry of Education (MOE) Tier 2 Grant (MOE-T2EP30220-0006). T.L. acknowledges support from the National Natural Science Foundation of China (31871959) and the National Key R&D Program of China (2022YFD1700200). Q.Y. acknowledges support from the National Natural Science Foundation of China (32161133010), the National Key R&D Program of China (2022YFD1700200) and the Shenzhen Science and Technology Program (KQTD20180411143628272). X.Q. and H.G. acknowledge support from the Singapore Ministry of Education (MOE) under its Academic Research Fund Tier 1 award no. RG138/20, no. RG135/22 and a start-up grant from Nanyang Technological University, Singapore and A*STAR, Singapore. G.Z and H.G. acknowledge funding support from the Ministry of Education in Singapore under grant MOE-MOET32022-0002. A.M. acknowledges support from the Singapore Ministry of Education (MOE) through an Academic Research (AcRF) Tier 3 grant (Grant No. MOE 2019-T3-1-012). We acknowledge the Facility for Analysis, Characterisation, Testing and Simulation (FACTS) and NTU Institute of Structural Biology (NISB), Nanyang Technological University, Singapore, for use of their HR-TEM, Cryo-TEM and NMR facilities. Molecular dynamics simulations reported were performed on resources provided by the High Performance Computing Centre at Nanyang Technological University, Singapore, and the National Supercomputing Centre, Singapore (http://www.nscc.sg).

Author information

Authors and Affiliations

Authors

Contributions

T.L., Q.Y., H.G. and J.Y. designed the study. Q.Y. conceptualized and supported the study. H.L., H.M., X.H., H.Q., F.Y., T.L. and J.Y. conducted the experiments. H.L. performed the experiment and analysis. X.Q. performed the modelling, simulations and analysis. H.L. and X.Q. collected the data. H.L., X.Q., H.M., X.H., H.Q., G.Z., A.M., Q.Y., T.L., H.G. and J.Y. analysed and interpreted the data. The paper was written through contributions of all authors. All authors have given approval of the final version of the paper for submission.

Corresponding authors

Correspondence to Tian Liu, Qing Yang, Huajian Gao or Jing Yu.

Ethics declarations

Competing interests

J.Y. and H.L. have filed a Singapore provisional patent application number 10202301815S.

Peer review

Peer review information

Nature Nanotechnology thanks Debasish Haldar and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.

Additional information

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Supplementary Information

Supplementary Methods, Tables 1–7 and Figs. 1–45.

Reporting Summary

Source data

Source Data Fig. 1

Statistical source data.

Source Data Fig. 2

Statistical source data.

Source Data Fig. 3

Statistical source data.

Source Data Fig. 4

Statistical source data.

Source Data Fig. 5

Statistical source data.

Source Data Fig. 6

Statistical source data.

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Li, H., Qian, X., Mohanram, H. et al. Self-assembly of peptide nanocapsules by a solvent concentration gradient. Nat. Nanotechnol. (2024). https://doi.org/10.1038/s41565-024-01654-w

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1038/s41565-024-01654-w

Search

Quick links

Nature Briefing: Translational Research

Sign up for the Nature Briefing: Translational Research newsletter — top stories in biotechnology, drug discovery and pharma.

Get what matters in translational research, free to your inbox weekly. Sign up for Nature Briefing: Translational Research