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From Proteopedia

Tobacco Etch Virus (TEV) Protease

The tobacco etch virus (TEV) is a member of the Potyviridae family of positive-strand RNA viruses ^[1]. The single-strand RNA genome of the TEV is translated into a large polyprotein precursor that is cleaved soon after translation to form independent protein products ^[2]. The TEV nuclear inclusion a (NIa) protease (shown to the right co-crystallized with peptide product in purple, with the catalytic residues highlighted as green ball and stick models) ^[3] is a 27 kDa 3C-type protease responsible for the processing of the original polyprotein into functional viral proteins. TEV protease resembles well-known serine proteases, such as trypsin and chymotrypsin, except that the TEV protease utilizes the nucleophilic thiol of the active site cysteine residue, as opposed to the serine hydroxyl used in serine proteases ^[4]. Ultimately, the biological importance of the TEV protease requires that the enzyme have very stringent sequence specificity to ensure proper production of viral proteins, and it is for this reason that the TEV protease has increasingly been used to remove affinity tags from recombinant proteins.

Structure of TEV Protease

TEV protease adopts a antiparallel β-barrel fold, typical of trypsin-like serine proteases, where the β sheet in the first domain is open (red) and the β sheet in the second domain folds to form a (cyan). Like typical serine proteases, the β-barrel contains a motif. Located at the interface between the two domains is the , composed of His46, Asp81, and Cys151. A structural comparison with related proteins reveals that the TEV protease fold is most similar to that of other 3C cysteine proteases from hepatitis A virus and rhinovirus, which serve a similar function as the TEV protease in their respective viruses. However, although the overall fold of TEV protease and these related proteins is indeed very similar, the actual atomic coordinates are very different, with the root mean square deviation for Cα carbons between 2.4 to 3.5 Å ^[5].

Substrate Specificity

The canonical recognition site of the TEV protease is the seven amino acid sequence ENLYFQ/G, with cleavage occurring after the glutamine residue. Although quite specific, TEV protease does have a tendency to undergo self-cleavage at a (KVFM/S) which follows residue 218, yielding a truncated enzyme with diminished catalytic activity ^[6]. Based on biochemical and structural data, it appears that the C-terminal region of the protein is relatively unstructured and flexible, allowing the scissile bond between Met218 and Ser219 to come dangerously close to the active site, and is readily cleaved. Mutation of Ser 219 to a number of other amino acids (Asp, Val, Pro) functions to limit the mobility of the peptide bond between residues 218 and 219, and has led to the production of TEV protease constructs resistant to this autoproteolytic activity with no affect in the normal catalytic function. Crystallization of the catalytically active TEV protease resistant to autoproteolysis (S219D mutation) in the presence of an artificial substrate revealed that the larger of the two products remain bound within the enzyme active site. Likewise, crystallization of an inactive TEV protease mutant (in which the catalytic Cys151 was mutated to Ala) has been carried out both in the presence and absence of artificial substrate. Interestingly, in the absence of artificial substrate, the (shown in yellow, active site residues in green) of the inactive TEV protease is bound within the active site of the enzyme, suggesting that the C-terminus of binds to the active site with high specificity and may be responsible for the diminished catalytic capacity of the truncated enzyme after autoproteolysis at residue 219 ^[7].

Links

To view available crystal structures of TEV protease please visit the following:

• 1lvm
• 1lvb
• 1q31

References

1. ↑ Ryan MD, Flint M. Virus-encoded proteinases of the picornavirus super-group. J Gen Virol. 1997 Apr;78 ( Pt 4):699-723. PMID:9129643
2. ↑ Stanway G. Structure, function and evolution of picornaviruses. J Gen Virol. 1990 Nov;71 ( Pt 11):2483-501. PMID:2254747
3. ↑ Phan J, Zdanov A, Evdokimov AG, Tropea JE, Peters HK 3rd, Kapust RB, Li M, Wlodawer A, Waugh DS. Structural basis for the substrate specificity of tobacco etch virus protease. J Biol Chem. 2002 Dec 27;277(52):50564-72. Epub 2002 Oct 10. PMID:12377789 doi:http://dx.doi.org/10.1074/jbc.M207224200
4. ↑ Seipelt J, Guarne A, Bergmann E, James M, Sommergruber W, Fita I, Skern T. The structures of picornaviral proteinases. Virus Res. 1999 Aug;62(2):159-68. PMID:10507325
5. ↑ Phan J, Zdanov A, Evdokimov AG, Tropea JE, Peters HK 3rd, Kapust RB, Li M, Wlodawer A, Waugh DS. Structural basis for the substrate specificity of tobacco etch virus protease. J Biol Chem. 2002 Dec 27;277(52):50564-72. Epub 2002 Oct 10. PMID:12377789 doi:http://dx.doi.org/10.1074/jbc.M207224200
6. ↑ Kapust RB, Tozser J, Fox JD, Anderson DE, Cherry S, Copeland TD, Waugh DS. Tobacco etch virus protease: mechanism of autolysis and rational design of stable mutants with wild-type catalytic proficiency. Protein Eng. 2001 Dec;14(12):993-1000. PMID:11809930
7. ↑ Nunn CM, Jeeves M, Cliff MJ, Urquhart GT, George RR, Chao LH, Tscuchia Y, Djordjevic S. Crystal structure of tobacco etch virus protease shows the protein C terminus bound within the active site. J Mol Biol. 2005 Jul 1;350(1):145-55. PMID:15919091 doi:10.1016/j.jmb.2005.04.013