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. 2005 Nov 4;102(46):16729–16734. doi: 10.1073/pnas.0506880102

Table 1. Comparative analysis between His-TAC and Y2H methods to efficiently reveal specific TRX/target complexes in trx1Δtrx2Δ yeast mutants.

Affinity chromatography*
Yeast two-hybrid
Targets TRX1 TRX2 Ath2 Ath3 TRX1 TRX2 Ath2 Ath3
AHP1 +++ +++ +++ +++ ++ +++ ++
TSA1 ++ + + NI ++++ NT
MET16 + + + NI +++ ++ ++
MSRA NI NI NI NI + ++ +/− +/−

All TRX baits are mutated and carry a CXXS active site. NT, not tested; Ath2, AtTrxh2; Ath3, AtTrxh3.

*

Plus signs (+, ++, +++), spot density as observed on 2D gels. NI, the corresponding target was not identified among the 2D spots analyzed.

Plus signs (+, ++, +++), the level of two-hybrid interactions; −, no interaction occurred between partners tested; +/−, a faint but reproducible interaction.