TY - JOUR
T1 - Custom design of protein particles as multifunctional biomaterials
AU - Shanbhag, Bhuvana K.
AU - Liu, Chang
AU - Pradeep, G. C.
AU - Younas, Tayyaba
AU - Hu, Kevin K.Y.
AU - Fulcher, Alex J.
AU - Struwe, Weston B.
AU - Steer, David
AU - Dumsday, Geoff
AU - Harper, Ian S.
AU - Kukura, Philipp
AU - Haritos, Victoria S.
AU - He, Lizhong
N1 - Funding Information:
B.K.S. and C.L. contributed equally to the work. B.K.S and C.L. acknowledge the Monash University Institute of Graduate Research for scholarship. C.L. acknowledges the travel grant provided by Faculty of Engineering, Monash University. P.G.C. acknowledges the New Horizon Research Scholarship provided by Faculty of Engineering, Monash University and Commonwealth Scientific and Industrial Research Organization (CSIRO), Australia. V.S.H. acknowledges the financial support from LIEF grant number LE16100185. B.K.S and L.H. acknowledges the support from the Australian Research Council (ARC) through the ARC Research Hub for Energy‐efficient Separation (IH170100009). The authors acknowledge the facilities of Monash Micro Imaging, Monash Centre for Electron Microscopy, The Clive and Ramaciotti Centre for Structural Cryo‐Electron Microscopy and Monash Biomedical Proteomics for their services. They thank Dr. Tim Ryan and Dr. Adrian Hawley from the Australian Synchrotron for technical support of SAXS work and Gina Pacheco Arredondo for her assistance with SAXS experiments.
Publisher Copyright:
© 2021 Wiley-VCH GmbH
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/1/10
Y1 - 2021/1/10
N2 - Assembled protein particles, as emerging biomaterials, have broad applications ranging from vaccines and drug delivery to biocatalysis and particle tracking, but to date these require trial-and-error rational design experimentation and/or intensive computational methods to generate. Here, the authors describe an easy-to-implement engineering strategy to generate customized protein particles as multifunctional biomaterials. They utilize protein–peptide modules to generate functional nanoparticles whose assembly and size is controlled by the addition of mild stimuli. The protein assembling method is versatile, as exemplified through particle formation with 7 distinct protein modules, using a variety of assembly conditions tailored by the chemistries of 3 peptide partners. They have generated customized protein particles using enzymes, binding and reporter proteins, and their functions and utilities are demonstrated using biocatalysis, sensing, and labelling applications, respectively. Furthermore, co-assembly with two functional proteins within one particle has been successfully achieved and demonstrated. Physical insights into the kinetics and molecular mechanisms of particle formation are revealed by small angle X-ray scattering and mass photometry, providing fundamental knowledge to guide design and manufacture these interesting biomaterials in future. Their protein assembling strategy is a reliable method for fabricating a protein particle to deliver new functionalities on-demand.
AB - Assembled protein particles, as emerging biomaterials, have broad applications ranging from vaccines and drug delivery to biocatalysis and particle tracking, but to date these require trial-and-error rational design experimentation and/or intensive computational methods to generate. Here, the authors describe an easy-to-implement engineering strategy to generate customized protein particles as multifunctional biomaterials. They utilize protein–peptide modules to generate functional nanoparticles whose assembly and size is controlled by the addition of mild stimuli. The protein assembling method is versatile, as exemplified through particle formation with 7 distinct protein modules, using a variety of assembly conditions tailored by the chemistries of 3 peptide partners. They have generated customized protein particles using enzymes, binding and reporter proteins, and their functions and utilities are demonstrated using biocatalysis, sensing, and labelling applications, respectively. Furthermore, co-assembly with two functional proteins within one particle has been successfully achieved and demonstrated. Physical insights into the kinetics and molecular mechanisms of particle formation are revealed by small angle X-ray scattering and mass photometry, providing fundamental knowledge to guide design and manufacture these interesting biomaterials in future. Their protein assembling strategy is a reliable method for fabricating a protein particle to deliver new functionalities on-demand.
KW - biocatalysis
KW - biosensing
KW - multi-functions
KW - protein particles
KW - protein self-assembly
KW - stimuli-responsive peptides
UR - http://www.scopus.com/inward/record.url?scp=85116358718&partnerID=8YFLogxK
U2 - 10.1002/adfm.202108039
DO - 10.1002/adfm.202108039
M3 - Article
AN - SCOPUS:85116358718
VL - 32
JO - Advanced Functional Materials
JF - Advanced Functional Materials
SN - 1616-301X
IS - 2
M1 - 2108039
ER -