Yellow fever virus NS2B/NS3 protease: Hydrolytic Properties and Substrate Specificity

• Published in: Biochemical and biophysical research communications Vol. 407; no. 4; pp. 640 - 644
• Main Authors: Kondo, Marcia Y., Oliveira, Lilian C.G., Okamoto, Debora N., de Araujo, Marina R.T., Duarte dos Santos, Claudia N., Juliano, Maria A., Juliano, Luiz, Gouvea, Iuri E.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 22-04-2011
• Subjects: Amino Acid Motifs; Dengue; Enzyme kinetics; Flavivirus; FRET substrate; Hydrogen-Ion Concentration; Hydrolysis; Peptides - chemistry; Recombinant Proteins - chemistry; Recombinant Proteins - genetics; RNA Helicases - chemistry; RNA Helicases - genetics; Serine Endopeptidases - chemistry; Serine Endopeptidases - genetics; Serine-proteases; Substrate Specificity; Viral Nonstructural Proteins - chemistry; Viral Nonstructural Proteins - genetics; West Nile virus; Yellow fever virus; Yellow fever virus - enzymology; FRET substrate; Enzyme kinetics; Flavivirus; Dengue; Serine-proteases
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2011.03.054

► YFV contains the same substrate motif in all processing sites. ► The kcat/km varied by more than two orders of magnitude among then. ► Obtained data parallel with those previously obtained in vivo. ► Substrates do not co-evolved with protease to promote highly efficient hydrolysis. ► Interactions others than on motif are critical in mediating substrate selective.
Here we report the hydrolytic behavior of recombinant YFV NS2B/NS3 protease against FRET substrates mimicking the prime and non-prime region of the natural polyprotein cleavage sites. While the P2-P′1 motif is the main factor associated with the catalytic efficiency of Dengue (DV) and West Nile Virus (WNV) protease, we show that the kcat/Km of YFV NS2B/NS3 varied by more than two orders of magnitude, despite the presence of the same motif in all natural substrates. The catalytic significance of this homogeneity – a unique feature among worldwide prominent flavivirus – was kinetically analyzed using FRET peptides containing all possible combinations of two and three basic amino acids in tandem, and Arg and Lys residues produced distinct effects on kcat/Km. The parallel of our data with those obtained in vivo by Chambers et al. (1991) restrains the idea that these sites co-evolved with the NS2B/NS3 protease to promote highly efficient hydrolysis and supports the notion that secondary substrate interaction distant from cleavage sites are the main factor associated with the different hydrolytic rates on YFV NS2B-NS3pro natural substrates.