Skip to main content
. 2013 Aug 20;14:18. doi: 10.1186/1471-2199-14-18

Table 2.

Panel of expression vectors encoding fusion proteins

Vector 5′-module Central module 3′-module
Set 1
 
 
 
pEF5/FRT-DEST-R4-R3_V5-6xHis: PAR2:mKate2
V5-6xHis
PAR-2
mKate2
pEF5/FRT-DEST-R4-R3_V5-6xHis: PAR2: EGFP
V5-6xHis
PAR-2
EGFP
Set 2
 
 
 
pEF5/FRT-DEST-R4-R3_mKate2: SIRT1
mKate2
SIRT1
SV40 polyA
pEF5/FRT-DEST-R4-R3_mKate2: ΔNtermSIRT1a
mKate2
ΔNtermSIRT1
SV40 polyA
Set 3
 
 
 
pEF5/FRT-DEST-R4-R3_mkate2: RelA:V5-6xHis
mKate2
p65
V5-6xHis
pEF5/FRT-DEST-R4-R3_V5-6xHis:p65:mKate2 V5-6xHis p65 mKate2

MultiSite Gateway recombination reactions were carried out between the adapted destination expression vector pEF5/FRT-DEST-R4-R3, and plasmids encoding 5′-module, the ORF of interest (central module) and the 3′-module as described. The resulting expression plasmids are listed on the table, with an indication of the functional modules used for making each fusion protein, and are organised in sets, according to the toolkit properties intended to illustrate (see main text). The central module encoding wt SIRT1 is an entry clone obtained from an ORFeome library, used in the MultiSite cloning reaction with no prior modifications. The SV40 polyA module (italics) does not encode for a peptide but contains a polyA signal that precedes the BGH polyA signal provided by the pEF5/FRT-DEST-R4-R3 vector.

aThe “Δ” symbol stands for “deleted”.