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. 2006 Sep 13;80(22):11283–11292. doi: 10.1128/JVI.00820-06

TABLE 4.

Stern-Volmer quenching constants for the association of N proteins from Sin Nombre, Andes, Puumala, Prospect Hill, and Seoul viruses with wild-type S segment panhandles from different viruses in binding buffer containing 80 mM NaCl at room temperaturea

Panhandle Quenching constant for interaction with indicated N protein
SNV Andes virus Puumala virus PHV Seoul virus
None 6.4 ± 0.1 7.2 ± 0.3 9.7 ± 0.4 7.9 ± 0.1 6.3 ± 0.1
Andes virus 2.8 ± 0.05 2.4 ± 0.03 4.2 ± 0.1 5.2 ± 0.3 3.3 ± 0.2
PHV 5.2 ± 0.1 2.7 ± 0.1 4.8 ± 0.3 4.9 ± 0.2 3.1 ± 0.2
Puumala virus 5.4 ± 0.1 2.7 ± 0.02 3.5 ± 0.1 5.4 ± 0.3 3.6 ± 0.1
Seoul virus 4.0 ± 0.3 3.0 ± 0.2 4.5 ± 0.2 5.1 ± 0.2 3.0 ± 0.3
SNV 2.6 ± 0.06 2.5 ± 0.1 4.3 ± 0.1 5.3 ± 0.2 3.3 ± 0.3
Bunyamwera virus 5.0 ± 0.3 5.9 ± 0.3 8.1 ± 0.4 7.1 ± 0.2 5.2 ± 0.1
Tomato spotted wilt virus 5.4 ± 0.2 6.2 ± 0.1 8.0 ± 0.2 7.3 ± 0.1 5.6 ± 0.1
Rift Valley fever virus 5.0 ± 0.3 6.3 ± 0.2 8.6 ± 0.3 7.7 ± 0.2 5.3 ± 0.2
CCHFV 4.9 ± 0.2 6.8 ± 0.3 8.8 ± 0.4 7.2 ± 0.2 5.9 ± 0.1
a

Tryptophan fluorescence of N protein (25 nM) was quenched with acrylamide in the presence or absence panhandle RNA to generate the Stern-Volmer plots. The panhandle RNA concentration was three times the dissociation constant for the panhandles used in each experiment. PHV, Prospect Hill virus; CCHFV, Crimean Congo hemorrhagic fever virus.