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. 2008 May 14;82(15):7601–7612. doi: 10.1128/JVI.00209-08

TABLE 3.

Summary of the biochemical and biological properties of Ls-eIF4E mutants

Class of mutation eIF4E form In vitro cap bindinga,b In vitro eIF4G bindingb Virus rescuec Yeast rescued
mo10 allele eIF4E0 + + + +
mo11 allele eIF4E1 ± NT +
mo12 allele eIF4E2 ± NT +
eIF4G binding E91A + ± + +
W94A + ± + +
G156A + ± + +
E157A + ± + −*
Cap binding W64A NT
W77L ± NT
W123A NT +
R173A + NT
W182A NT
S223L + NT + +
Outer surface F65A ± NT
R82L + NT + +
Y113A + NT + +
A174P ± NT + −*
a

Estimated by cap affinity chromatography.

b

+, present; −, absent; ±, binding is affected, but not fully abolished; NT, not tested.

c

+, the eIF4E form is able to complement LMV infection in resistant plants; −, no complementation occurs.

d

10× serial dilutions of yeast strain J055 transformed with plasmids p426GPD-4E were plated on glucose selective medium. +, 100× or 1,000× dilutions grew on glucose-containing medium; -, these dilutions did not grow (behavior was identical to that of the negative control, cells transformed with the plasmid p426GPD); *, in only one experiment of 4 did cells grow for a 10× dilution, but none grew for the 100× and 1,000× serial dilutions.