A simple and high efficiency purification of His-tagged turnip yellow mosaic virus-like particle (TYMV-VLP) by nickel ion affinity precipitation

• Published in: Journal of virological methods Vol. 319; p. 114771
• Main Authors: Tan, Foo Hou, Ng, Jeck Fei, Mohamed Alitheen, Noorjahan Banu, Muhamad, Azira, Yong, Chean Yeah, Lee, Khai Wooi
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.09.2023
• Subjects: affinity chromatography; chlorides; coat proteins; dialysis; Escherichia coli; immunogenicity; nanobiotechnology; nickel; Nickel affinity precipitation; Poly-histidine tagged protein; sucrose; transmission electron microscopy; Turnip yellow mosaic virus; Turnip yellow mosaic virus (TYMV); turnips; TYMV coat protein; TYMVc; ultracentrifugation; vaccine development; viruses; VLP purification; Poly-histidine tagged protein; TYMVc; VLP purification; TYMV coat protein; Turnip yellow mosaic virus (TYMV); Nickel affinity precipitation
• ISSN: 0166-0934; 1879-0984; 1879-0984
• DOI: 10.1016/j.jviromet.2023.114771

Virus-like particles (VLPs) is one of the most favourable subjects of study, especially in the field of nanobiotechnology and vaccine development because they possess good immunogenicity and self-adjuvant properties. Conventionally, VLPs can be tagged and purified using affinity chromatography or density gradient ultracentrifugation which is costly and time-consuming. Turnip yellow mosaic virus (TYMV) is a plant virus, where expression of the viral coat protein (TYMVc) in Escherichia coli (E. coli) has been shown to form VLP. In this study, we report a non-chromatographic method for VLP purification using C-terminally His-tagged TYMVc (TYMVcHis6) as a protein model. Firstly, the TYMVcHis6 was cloned and expressed in E. coli. Upon clarification of cell lysate, nickel (II) chloride [NiCl2; 15 µM or equivalent to 0.0000194% (w/v)] was added to precipitate TYMVcHis6. Following centrifugation, the pellet was resuspended in buffer containing 1 mM EDTA to chelate Ni2+, which is then removed via dialysis. A total of 50% of TYMVcHis6 was successfully recovered with purity above 0.90. Later, the purified TYMVcHis6 was analysed with sucrose density ultracentrifugation, dynamic light scattering (DLS), and transmission electron microscopy (TEM) to confirm VLP formation, which is comparable to TYMVcHis6 purified using the standard immobilized metal affinity chromatography (IMAC) column. As the current method omitted the need for IMAC column and beads while significantly reducing the time needed for column washing, nickel affinity precipitation represents a novel method for the purification of VLPs displaying poly-histidine tags (His-tags). •TYMV is a plant virus, where expression of the viral coat protein (TYMVc) in Escherichia coli (E. coli) has been shown to form VLP.•Nickel ion affinity precipitation is a novel approach for VLP purification without chromatography or high-end centrifuges.•Nickel ion affinity precipitation method precipitates his-tagged multimeric VLPs.