Cargando…
Dendrimer‐Like Supramolecular Assembly of Proteins with a Tunable Size and Valency Through Stepwise Iterative Growth
The assembly of proteins in a programmable manner provides insight into the creation of novel functional nanomaterials for practical applications. Despite many advances, however, a rational protein assembly with an easy scalability in terms of size and valency remains a challenge. Here, a simple bot...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8693032/ https://www.ncbi.nlm.nih.gov/pubmed/34719882 http://dx.doi.org/10.1002/advs.202102991 |
_version_ | 1784619059151634432 |
---|---|
author | Bae, Jin‐Ho Kim, Hong‐Sik Kim, Gijeong Song, Ji‐Joon Kim, Hak‐Sung |
author_facet | Bae, Jin‐Ho Kim, Hong‐Sik Kim, Gijeong Song, Ji‐Joon Kim, Hak‐Sung |
author_sort | Bae, Jin‐Ho |
collection | PubMed |
description | The assembly of proteins in a programmable manner provides insight into the creation of novel functional nanomaterials for practical applications. Despite many advances, however, a rational protein assembly with an easy scalability in terms of size and valency remains a challenge. Here, a simple bottom‐up approach to the supramolecular protein assembly with a tunable size and valency in a programmable manner is presented. The dendrimer‐like protein assembly, simply called a “protein dendrimer,” is constructed through a stepwise and alternate addition of a building block protein. Starting from zeroth‐generation protein dendrimer (pG(0)) of 27 kDa, the protein dendrimer is sequentially grown to pG(1), pG(2), pG(3), to pG(4) with a molecular mass of 94, 216, 483, and 959 kDa, respectively. The valency of the protein dendrimers at the periphery increases by a factor of two after each generation, allowing a tunable valency and easy functionalization. The protein dendrimers functionalizes with a targeting moiety and a cytotoxic protein cargo shows a typical feature of multi‐valency in the avidity and a highly enhanced cellular cytotoxicity, exemplifying their utility as a protein delivery platform. The present approach can be effectively used in the creation of protein architectures with new functions for biotechnological and medical applications. |
format | Online Article Text |
id | pubmed-8693032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86930322022-01-03 Dendrimer‐Like Supramolecular Assembly of Proteins with a Tunable Size and Valency Through Stepwise Iterative Growth Bae, Jin‐Ho Kim, Hong‐Sik Kim, Gijeong Song, Ji‐Joon Kim, Hak‐Sung Adv Sci (Weinh) Research Articles The assembly of proteins in a programmable manner provides insight into the creation of novel functional nanomaterials for practical applications. Despite many advances, however, a rational protein assembly with an easy scalability in terms of size and valency remains a challenge. Here, a simple bottom‐up approach to the supramolecular protein assembly with a tunable size and valency in a programmable manner is presented. The dendrimer‐like protein assembly, simply called a “protein dendrimer,” is constructed through a stepwise and alternate addition of a building block protein. Starting from zeroth‐generation protein dendrimer (pG(0)) of 27 kDa, the protein dendrimer is sequentially grown to pG(1), pG(2), pG(3), to pG(4) with a molecular mass of 94, 216, 483, and 959 kDa, respectively. The valency of the protein dendrimers at the periphery increases by a factor of two after each generation, allowing a tunable valency and easy functionalization. The protein dendrimers functionalizes with a targeting moiety and a cytotoxic protein cargo shows a typical feature of multi‐valency in the avidity and a highly enhanced cellular cytotoxicity, exemplifying their utility as a protein delivery platform. The present approach can be effectively used in the creation of protein architectures with new functions for biotechnological and medical applications. John Wiley and Sons Inc. 2021-10-31 /pmc/articles/PMC8693032/ /pubmed/34719882 http://dx.doi.org/10.1002/advs.202102991 Text en © 2021 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Bae, Jin‐Ho Kim, Hong‐Sik Kim, Gijeong Song, Ji‐Joon Kim, Hak‐Sung Dendrimer‐Like Supramolecular Assembly of Proteins with a Tunable Size and Valency Through Stepwise Iterative Growth |
title | Dendrimer‐Like Supramolecular Assembly of Proteins with a Tunable Size and Valency Through Stepwise Iterative Growth |
title_full | Dendrimer‐Like Supramolecular Assembly of Proteins with a Tunable Size and Valency Through Stepwise Iterative Growth |
title_fullStr | Dendrimer‐Like Supramolecular Assembly of Proteins with a Tunable Size and Valency Through Stepwise Iterative Growth |
title_full_unstemmed | Dendrimer‐Like Supramolecular Assembly of Proteins with a Tunable Size and Valency Through Stepwise Iterative Growth |
title_short | Dendrimer‐Like Supramolecular Assembly of Proteins with a Tunable Size and Valency Through Stepwise Iterative Growth |
title_sort | dendrimer‐like supramolecular assembly of proteins with a tunable size and valency through stepwise iterative growth |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8693032/ https://www.ncbi.nlm.nih.gov/pubmed/34719882 http://dx.doi.org/10.1002/advs.202102991 |
work_keys_str_mv | AT baejinho dendrimerlikesupramolecularassemblyofproteinswithatunablesizeandvalencythroughstepwiseiterativegrowth AT kimhongsik dendrimerlikesupramolecularassemblyofproteinswithatunablesizeandvalencythroughstepwiseiterativegrowth AT kimgijeong dendrimerlikesupramolecularassemblyofproteinswithatunablesizeandvalencythroughstepwiseiterativegrowth AT songjijoon dendrimerlikesupramolecularassemblyofproteinswithatunablesizeandvalencythroughstepwiseiterativegrowth AT kimhaksung dendrimerlikesupramolecularassemblyofproteinswithatunablesizeandvalencythroughstepwiseiterativegrowth |