Functional decoration of elastin-like polypeptides-based nanoparticles with a modular assembly via isopeptide bond formation

被引:0
|
作者
Yamaguchi, Jun [1 ]
Nishida, Kei [1 ]
Kobatake, Eiry [1 ]
Mie, Masayasu [1 ]
机构
[1] Inst Sci Tokyo, Sch Life Sci & Technol, Dept Life Sci & Technol, 4259 Nagatsuta Cho,Midori Ku, Yokohama 2268501, Japan
基金
日本学术振兴会;
关键词
Elastin-like polypeptide; Isopeptide bond formation; Protein ligation; Protein nanoparticles; SnoopTag/SnoopCatcher; PROTEIN NANOPARTICLES; LUCIFERASE; DRUG;
D O I
10.1007/s10529-024-03549-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Temperature-responsive elastin-like polypeptides (ELPs) exhibit a low critical solution temperature-type phase transition and offer potential as useful materials for the construction of nanoparticles. Herein, we developed a novel decoration method for ELP-based nanoparticles via isopeptide bond formation with the SnoopTag/SnoopCatcher system that is not affected by the heating process required for particle formation. A mixture of a fusion protein of ELP and poly(aspartic acid) (poly(D)), known as ELP-poly(D), and ELP-poly(D) fused with SnoopCatcher (ELP-poly(D)-SnC) formed protein nanoparticles as a result of the temperature responsiveness of ELP, with the resultant nanoparticles displaying the SnoopCatcher binding domain on their surfaces. In the present study, two model proteins fused to SnoopTag were displayed on the surfaces of protein nanoparticles constructed from ELP-poly(D)-SnC and ELP-poly(D). The model proteins are enhanced green fluorescent protein (EGFP) and Renilla luciferace (Rluc), which exhibits luminescent capability and weak thermostability, respectively. EGFP on the particle surface was found to retain 48.7% activity, while Rluc exhibited almost full activity, as calculated from the binding efficiency and nanoparticle activities recovered after purification. ELP-based nanoparticles containing the SnoopTag/SnoopCatcher system offer the opportunity for particle decoration with a wide range of functional proteins via isopeptide bond formation.
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页数:12
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