TY - JOUR
T1 - Reversible Assembly of an Artificial Protein Nanocage Using Alkaline Earth Metal Ions
AU - Ohara, Naoya
AU - Kawakami, Norifumi
AU - Arai, Ryoichi
AU - Adachi, Naruhiko
AU - Moriya, Toshio
AU - Kawasaki, Masato
AU - Miyamoto, Kenji
N1 - Funding Information:
The authors thank Prof. Toshiya Senda for managing cryo-EM data collections, Satomi Kojima for technical support of TEM observation, and Prof. Nobutaka Shimizu and Photon Factory (PF) staff for their help in synchrotron SAXS experiments, which were performed at PF, KEK, under the approval of PF program advisory committee (proposal number 2020G674). This research was supported by Platform Project for Supporting Drug Discovery and Life Science Research (Basis for Supporting Innovative Drug Discovery and Life Science Research (BINDS)) from AMED under Grant Number JP21am0101071/JP22ama121001 (support number 1582), JSPS KAKENHI Grant Number JP18K05324 to N.K., Grant Numbers JP17KK0104 and JP19H02522 to R.A., and Grant Number JP22J13988 to N.O., The Japan Association for Chemical Innovation (JACI) eighth Research Encouragement Award to N.K., and the Keio University Doctorate Student Grant-in-Aid Program from Ushioda Memorial Fund and KLL 2021 Ph.D. Program Research Grant to N.O.
Publisher Copyright:
© 2022 American Chemical Society.
PY - 2023/1/11
Y1 - 2023/1/11
N2 - Protein nanocages are of increasing interest for use as drug capsules, but the encapsulation and release of drug molecules at appropriate times require the reversible association and dissociation of the nanocages. One promising approach to addressing this challenge is the design of metal-dependent associating proteins. Such designed proteins typically have Cys or His residues at the protein surface for connecting the associating proteins through metal-ion coordination. However, Cys and His residues favor interactions with soft and borderline metal ions, such as Au+ and Zn2+, classified by the hard and soft acids and bases concept, restricting the types of metal ions available to drive association. Here, we show the alkaline earth (AE) metal-dependent association of the recently designed artificial protein nanocage TIP60, which is composed of 60-mer fusion proteins. The introduction of a Glu (hard base) mutation to the fusion protein (K67E mutant) prevented the formation of the 60-mer but formed the expected cage structure in the presence of Ca, Sr, or Ba ions (hard acids). Cryogenic electron microscopy (cryo-EM) analysis indicated a Ba ion at the interface of the subunits. Furthermore, we demonstrated the encapsulation and release of single-stranded DNA molecules using this system. Our results provide insights into the design of AE metal-dependent association and dissociation mechanisms for proteins.
AB - Protein nanocages are of increasing interest for use as drug capsules, but the encapsulation and release of drug molecules at appropriate times require the reversible association and dissociation of the nanocages. One promising approach to addressing this challenge is the design of metal-dependent associating proteins. Such designed proteins typically have Cys or His residues at the protein surface for connecting the associating proteins through metal-ion coordination. However, Cys and His residues favor interactions with soft and borderline metal ions, such as Au+ and Zn2+, classified by the hard and soft acids and bases concept, restricting the types of metal ions available to drive association. Here, we show the alkaline earth (AE) metal-dependent association of the recently designed artificial protein nanocage TIP60, which is composed of 60-mer fusion proteins. The introduction of a Glu (hard base) mutation to the fusion protein (K67E mutant) prevented the formation of the 60-mer but formed the expected cage structure in the presence of Ca, Sr, or Ba ions (hard acids). Cryogenic electron microscopy (cryo-EM) analysis indicated a Ba ion at the interface of the subunits. Furthermore, we demonstrated the encapsulation and release of single-stranded DNA molecules using this system. Our results provide insights into the design of AE metal-dependent association and dissociation mechanisms for proteins.
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U2 - 10.1021/jacs.2c09537
DO - 10.1021/jacs.2c09537
M3 - Article
C2 - 36541447
AN - SCOPUS:85145054432
SN - 0002-7863
VL - 145
SP - 216
EP - 223
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 1
ER -