Introduction

Self-assembly is the spontaneous organisation of individual subunits without central direction. A self-assembling protein scaffold offers an elegant method of spatially organising enzymes for co-localisation. Other approaches for enzyme scaffolding include the use of microcompartments, DNA and RNA scaffolds and fusions of aptamer domains¹. We designed experiments to investigate two distinct assembly processes for our enzyme-scaffold complex: the oligomerisation of alpha prefoldin and beta prefoldin, and the formation of isopeptide bonds between SpyTags and SnoopTags and SpyCatchers and SnoopCatchers respectively.

Alpha prefoldin (aPFD) (15.7 kDa) and beta prefoldin (bPFD) (13.8 kDa) derived from Methanobacterium thermoautotrophicum oligomerise to form heterohexameric structures (87 kDa), consisting of 2 alpha subunits and 4 beta subunits². The prefoldin hexamer is assembled through interactions between beta hairpins in each subunit. These beta hairpins form two 8 stranded up and down beta barrels. Appropriate methods for analysing the assembly of prefoldin hexamers include techniques such as Size Exclusion Chromatography (SEC), Native-PAGE and Multiangle Light Scattering (MALS), as these retain the native structure of assemblies and can distinguish between molecules of varying size. SEC was used to demonstrate the formation of aPFD and bPFD hexamers and other oligomers, and also could enable the investigation of the monodispersity of the sample. We also aimed to investigate if aPFD and bPFD could hexamerise when fused with SpyCatcher or SnoopCatcher.

Figure 1: aPFD and bPFD form hexamers. Image created using PDB ID: 1FXK²

The SpyCatcher and SpyTag system were derived from Streptococcus pyogenes fibronectin-binding protein FbaB³. A spontaneous isopeptide bond forms between a lysine residue on the SpyCatcher protein and an aspartic acid on the SpyTag peptide, covalently fusing the two components. Fusion of the SpyCatcher and SpyTag to different proteins enables their spontaneous covalent conjugation within minutes. A similar attachment mechanism was developed from the adhesin RrgA from Streptococcus pneumoniae, yielding SnoopCatcher and SnoopTag which also covalently bind to each other⁴. In addition, the attachment systems are orthogonal, as SnoopTag/SnoopCatcher does not interact with SpyTag/SpyCatcher.

Figure 2: A spontaneous isopeptide bond forms between SpyTag and SpyCatcher. Image created using PDB ID: 4MLS⁵

The use of both systems in tandem enable specific and irreversible attachment of tagged enzymes with aPFD fused to SpyCatcher or bPFD fused to SnoopCatcher. The prefoldins can then self-assemble to form an enzyme-scaffold complex. SDS-PAGE was employed to investigate the Tag/Catcher reaction, as the sodium dodecyl sulphate and heat treatment before analysis denatures proteins, while retaining covalent interactions. Any covalent interaction between an enzyme and a prefoldin-catcher fusion could be determined, indicating the binding of an enzyme to our scaffold.

Gamma prefoldin (gPFD) filaments was proposed as an alternative scaffold to alpha and beta prefoldin hexamers. These filaments are composed of a single protein, related to aPFD and bPFD, that polymerises linearly⁶. Although it is difficult to control the length of filaments^7,8 and the distribution of a mixture of fusions with SpyCatcher or SnoopCatcher, the filaments enable increased density of enzyme clustering. To investigate if gPFD filaments are able to form when fused to SpyCatcher and/or SpyCatcher and a SpyTagged enzyme, Transmission Electron Microscopy (TEM) was used to image gPFD, gPFD fused to SpyCatcher (gPFD-SpyC) and gPFD-SpyC mixed with a SpyTagged enzyme (IaaH-SpyT).

SEC, SDS-PAGE and TEM provide valuable information about the required conditions for assembly of our enzyme-scaffold complex. A multiplexed approach to the characterisation of the assembly process enable us to piece together a more complete understanding of the enzyme scaffold and its potential applications to industry and foundational research.

Aims

To investigate and demonstrate:

• the assembly of alpha prefoldin and beta prefoldin hexamers, in their native state or when fused with SpyCatcher or SnoopCatcher
• SpyTag/SpyCatcher or SnoopTag/SnoopCatcher reactions between prefoldin scaffold proteins and tagged enzymes

Methods

Assembly of alpha prefoldin and beta prefoldin

IMAC purified alpha prefoldin and beta prefoldin were mixed in a 1:2 molar ratio to a total volume of 1 mL at concentrations of 1 mg/mL in PBS pH 8 and incubated overnight at 4oC. Size Exclusion Chromatography was kindly performed by Ms Hélène Lebhar. Alpha prefoldin, beta prefoldin and the mixture were loaded onto a Superdex S200 Increase 10/300 GL column using an AKTA start, and separated by SEC. The chromatograms of the three runs were then overlayed for analysis, and compared to the molecular weight standards thyroglobulin (670 kDa), gamma-globulin (158 kDa), ovalbumin (44 kDa) and myoglobulin (17 kDa).

SpyTag/SpyCatcher reactions

IaaH fused with SpyTag and proteins fused to SpyCatcher (aPFD-SpyCatcher, gPFD-SpyCatcher and SpyCatcher-gPFD-SpyCatcher) were mixed at a concentration of 3 µM and 15 µM respectively in a total volume of 250 µL in PBS pH 8, and incubated at room temperature. After 0, 10, 20 and 30 minutes of incubation, a 10 µL sample was taken and boiled with 5 µL of 4x Bolt LDS sample buffer for 10 minutes at 95oC to cease SpyCatcher reactivity while preserving any covalent interactions. The samples were then examined on SDS-PAGE.

Transmission Electron Microscopy (TEM)

Wild type gamma prefoldin and gamma prefoldin fused to SpyCatcher samples were diluted to 0.01 mg/mL. Gamma prefoldin fused to SpyCatcher and reacted with IaaH-SpyTag as previously described were also diluted to 0.01 mg/mL of gamma prefoldin. Protein samples were negative-stained on carbon coated grids and imaged with TEM, using a JEOL JEM-1400 with magnifications up to 150000x. Grid staining and TEM was kindly performed by Dr Daniel Lorenz Winter.