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An In Vivo Photo-Cross-Linking Approach Reveals a Homodimerization Domain of Aha1 in S. cerevisiae


Protein-protein interactions play an essential role in almost any biological processes. Therefore, there is a particular need for methods which describe the interactions of a defined target protein in its physiological context. Here we report a method to photo-cross-link interacting proteins in S. cerevisiae by using the non-canonical amino acid p-azido-L-phenylalanine (pAzpa). Based on the expanded genetic code the photoreactive non-canonical amino acid pAzpa was site-specifically incorporated at eight positions into a domain of Aha1 that was previously described to bind Hsp90 in vitro to function as a cochaperone of Hsp90 and activates its ATPase activity. In vivo photo-cross-linking to the cognate binding partner of Aha1 was carried out by irradiation of mutant strains with UV light (365 nm) to induce covalent intermolecular bonds. Surprisingly, an interaction between Aha1 and Hsp90 was not detected, although, we could confirm binding of suppressed pAzpa containing Aha1 to Hsp90 by native co-immunoprecipitation. However, a homodimer consisting of two covalently crosslinked Aha1 monomers was identified by mass spectrometry. This homodimer could also be confirmed using p-benzoyl-L-phenylalanine, another photoreactive non-canonical amino acid. Crosslinking was highly specific as it was dependent on irradiation using UV light, the exact position of the non-canonical amino acid in the protein sequence as well as on the addition of the non-canonical amino acid to the growth medium. Therefore it seems possible that an interaction of Aha1 with Hsp90 takes place at different positions than previously described in vitro highlighting the importance of in vivo techniques to study protein-protein interactions. Accordingly, the expanded genetic code can easily be applied to other S. cerevisiae proteins to study their interaction under physiological relevant conditions in vivo.


To understand the molecular machinery of a cell, methods for the study of protein-protein interactions are essential. The interactome of S. cerevisiae was initially explored using the yeast two-hybrid method [1], [2]. Later, high-throughput techniques like tandem-affinity purification combined with mass spectrometry were applied which generated a plethora of data [3]. These studies have contributed greatly to the understanding of the interactome of S. cerevisiae. Unfortunately, these methods do not capture the interaction of the protein of interest in the in vivo context, the large fusion tag might interfere with the protein function and they are not able to detect transient interactions. Hence, novel methods are needed which offer the opportunity to study protein-protein interactions in the physiological context. In addition, as modifications of the protein of interest like large tags used for tandem affinity purification can lead to changes in structure and function they should be kept as small as possible.

For this purpose the expanded genetic code represents a promising approach to establish novel methods for the analysis of protein-protein interactions. Using the expanded genetic code non-canonical amino acids with novel and unique properties can be incorporated into proteins at defined position in vivo using orthogonal suppressor tRNA and amino-acyl tRNA synthetase pairs [4]. Many different fields of application using non-canonical amino acids were already demonstrated like photocleavage of the polypeptide backbone [5], control of protein phosphorylation [6] or modification of a growth hormone with improved clinical performance [7]. To date the expanded genetic code is already established in different organisms including E. coli [8], S. cerevisiae [9], [10], P. pastoris [11], C. albicans [12] and mammalian cell lines like Chinese hamster ovary cells [13]. Among dozens of different non-canonical amino acids, there are basically three different types of photoreactive groups, including azido-, diazirin- and benzoyl-groups, which can be incorporated into proteins using the expanded genetic code [14], [15]. For photo-cross-link experiments the non-canonical amino acid pBzpa is widely used to covalently capture the interaction of two proteins [13], [16], [17], [18], [19], [20], [21], [22]. The reason for this is that photolysis of the keto group within the benzophenone can be induced with a relative long wavelength (350–365 nm). It reacts solely with C-H bonds and in case of no reaction this group is able to regenerate [16], [23]. The non-canonical amino acid pAzpa has not yet been widely applied for photo-cross-link experiments in vivo [24], [25]. However, pAzpa has the advantage over pBzpa that pAzpa is smaller in size than pBzpa, but can also be activated at 365 nm. Following activation using UV-light a short-lived (∼1 ns) nitrene is formed which is able to form covalent crosslinks with a variety of different chemicals groups. If no interacting partner is available in close vicinity, the group reacts with H2O which reduces false positive crosslinks [24], [25], [26].

In the present study we examine the possibility of using the non-canonical amino acid p-azido-L-phenylalanine to study protein-protein interactions in S. cerevisiae. By now, using the expanded genetic code and pAzpa for photo-cross-linking yet no studies are reported which use a full length protein for protein-protein analysis in vivo. For this purpose we chose the well characterized cochaperone Aha1 (activator of Hsp90 ATPase) [27]. Aha1 binds as a monomer to the Hsp90 homodimer. The binding of the Aha1 N-terminal domain to the middle domain of Hsp90 induces a conformational change in Hsp90. This stimulates the ATPase activity of both Hsp90 proteins within the homodimer [28]. The interaction interface of the Aha1 N-terminal domain with the Hsp90 middle domain was characterized by crystallography [29].

Accordingly we specifically incorporated p-azido-L-phenylalanine at eight different positions within the binding domain of Aha1 to Hsp90 as suggested by the crystal structure. We confirmed the interaction of the Aha1 variants to Hsp90 by native co-immunoprecipitation. In contrast to the expected Hsp90 and Aha1 heterodimer, a homodimer consisting of two covalently crosslinked Aha1 monomers was identified by mass spectrometry and confirmed by an immunological approach. In addition, this homodimer was also reproduced using the photoreactive amino acid p-benzoyl-L-phenylalanine.


Site-specific incorporation of pAzpa in to Aha1

For the characterization and application of the expanded genetic code to study protein-protein interactions in S. cerevisiae we used the well characterized interaction of Aha1 with Hsp90. Aha1 has been described as a cochaperone that binds to Hsp90 and strongly stimulates its ATPase activity [27], [30]. In S. cerevisiae two proteins are expressed Hsp82 and Hsc82 which both belong to the Hsp90 family. They are redundant in function and nearly identical in protein sequence [31]. The interaction between the N-terminal domain of yeast Aha1 (N-Aha1: residues 1–153) and the middle domain of yeast Hsp90 (M-Hsp90: residues 273–530) has been resolved by a crystal structure (Figure 1A) [29]. The hydrophobic side chains of Ile 64, Leu 66 and Phe 100 of Aha1 are suggested to be involved in the core interaction between the N-Aha1 and M-Hsp90. The side chains of the completely conserved motif 59-RKGK-62 among members of the Aha1 family are reported to be orientated towards Hsp90 and stabilize the catalytic loop of Hsp90 in its active conformation [29]. Based on these observations we chose the amino acids 59–66 for substitution with pAzpa to capture an interaction by a covalent crosslink (Figure 1A and B). The Aha1 variants containing an amber codon at the selected positions for suppression were additionally tagged using a V5 epitope and expressed under the control of the GAL1 promoter from a 2 µ plasmid. The orthogonal pair consisting of an E. coli amber suppressor tRNA and p-azido-L-phenylalanyl tRNA synthetase (aaRS) necessary for the incorporation of pAzpa were also expressed from a 2 µ plasmid based system [10].

Figure 1. Site-specific incorporation of pAzpa in Aha1.

A. Crystal structure of a complex between the middle segment of Hsp90 (M-Hsp90: residues 272–530) and the N-terminal domain of Aha1 (N-Aha1: residues 1–153) deposited at PDB (1USU). The region (59–66) for the incorporation of the non-canonical amino acid within N-Aha1 is highlighted in red. B. Chemical structure of pAzpa and pBzpa. C. Expression of Aha1 in the presence and absence of the non-canonical amino acid pAzpa incorporated at the indicated positions.

Surprisingly, during our suppression experiments we observed growth deficits of S. cerevisiae strain YPH501 in medium containing the non-canonical amino acid pAzpa. Inoculation of the wild type strain YPH501 at a low cell density of OD600 = 0.0003 in SC medium containing 2% glucose with various pAzpa concentrations resulted in a significantly inhibited growth rate of cells depending on pAzpa concentration (Figure S1A). This finding indicates an inhibitory effect of the non-canonical amino acid pAzpa. Furthermore, the growth rate of a strain expressing the orthogonal pair (2YA6,64C1) was significantly decreased depending on the pAzpa concentration added to the medium compared to the wild type strain YPH501 (Figure S1B). When pAzpa was replaced by the non-canonical amino acid pBzpa (Figure S1C) the growth rate of the strain was comparable to that of the wild type YPH501. These results indicate that the non-canonical amino acid pAzpa alone and more pronounced in combination with the orthogonal pair leads to adverse effects on growth of S. cerevisiae strain YPH501. A similar observation was made for another S. cerevisiae strain INVsc1 (data not shown). However, when medium was inoculated with high cell density (OD600 = 1) no growth deficits or morphological phenotypes were observed compared with the inoculation described in Figure S1 (data not shown). Accordingly, in the most cases it is sufficient when the expression of the model protein is induced to a specific time point in a dense preculture by adding pAzpa to the medium as described in this study.

Depending on the addition of pAzpa to the medium expression of the eight Aha1 variants containing pAzpa at the defined positions could be clearly detected (Figure 1C). Nevertheless, we observed also some background suppression in the absence of pAzpa. However, depending on the addition of pAzpa to the medium we saw a significantly stronger suppression of the amber stop codon for each Aha1 variant.

To test the availability and reactivity of the azido group incorporated into the Aha1 variant after 24 h of expression two highly chemoselective reactions, the Staudinger ligation and the azide-alkyne cycloaddition (Click Chemistry) [32] were applied for suppressed Aha1 I64X. On the basis of a specific reaction of the azido group with phosphine or alkyne groups various molecules were linked to Aha1 I64X including a triarylphosphine fluorescent dye that was site-specifically coupled to Aha1 I64X by the Staudinger ligation in a crude cell lysate (Figure S2A). In addition, the Cu(I)-catalyzed azide-alkyne cycloaddition was successfully applied for coupling a biotin molecule to immunoprecipitated Aha1 I64X (Figure S2B). These experiments also indicate stability of the azido group to different buffers and environments.

The substitution of one canonical amino acid by a non-canonical amino acid like pAzpa into the Aha1 protein might influence the three-dimensional (3D)-conformation. This change in conformation might than result in artificial or loss of interactions. To verify that the expressed and modified Aha1 variants were still able to interact with Hsp90, we performed native co-immunoprecipitation. Aha1 variants were precipitated using anti-V5 antibodies and their interaction with Hsp90 was detected by immunoblotting (Figure 2). For all Aha1 variants an interaction with Hsp90 was observed. These results indicate that the replacement of the original canonical amino acids by pAzpa had no negative impact on the interaction between Aha1 variants and Hsp90. When whole protein lysates were separated using 8% polyacrylamide gel two bands were detected with the anti-Hsp90 antibody due to the higher resolution of separation for highly similar Hsp82 and Hsc82 proteins (Figure 2. Hsp90 Input).

Figure 2. Interaction of pAzpa-containing Aha1 variants with Hsp90.

Aha1 variants were expressed in the presence of pAzpa and subsequently immunoprecipitated via their V5-tag. Associated Hsp90 was detected by immunoblotting. Strain 2YA0C1 carrying the empty pYES2/CT vector was used as a control (c). Input = whole protein lysate; IP = eluate after immunoprecipitation.

Crosslink formation of Aha1

For photo-cross-linking, cells containing the various Aha1 variants and the orthogonal pair were irradiated for 120 min with UV light (365 nm) after 24 hours expression of the Aha1 variants in medium containing galactose and 1 mM pAzpa. Subsequently, proteins were isolated and analyzed by Western blot. The incorporation of pAzpa at the positions 59, 62, 64 and 66 combined with irradiation resulted in the formation of a crosslinked product (Figure 3A). This crosslink product had an apparent molecular weight of approximately 100 kDa and was depending on UV irrediation, the position of substitution within the protein as well as the addition of the non-canonical amino acid pAzpa (Figure S3). No additional crosslinked products could be observed. The amount of crosslink product depends on time of exposure and concentration of pAzpa as reduction of exposure time or lower pAzpa concentration in the medium resulted in decreased crosslink yields (Figure S4). We could not observe spontaneous crosslink product formation for pAzpa without exposure to UV light as reported by Grunbeck [33]. Aryl-azides are usually irradiated with UV light at wavelengths below 310 nm [16], [34]. However, in agreement with Takimoto and co-workers who have shown that the azido group can also be activated at longer wavelengths we photo-cross-linked at 365 nm [25]. Since shorter wavelengths have more energy than longer wavelengths we compared 312 nm and 365 nm wavelength induction with respect to formation of crosslink product after 120 min of irradiation. However we were not able to detect any difference regarding specificity and yield (data not shown).

Figure 3. In vivo crosslinking of Aha1 variants.

A. Following incubation in medium containing pAzpa, cells were exposed to UV light and cell lysates were analyzed by Western blot. The band at 100-canonical amino acid pBzpa was incorporated at position 64. Aha1 variant with pAzpa at position 59 was used as a positive control.

In addition to pAzpa there are additional photoreactive non-canonical amino acids with photo-crosslink properties which can be incorporated into proteins using the expanded genetic code [4]. Among them is p-benzoyl-L-phenylalanine (pBzpa) (Figure 1B). The benzophenone group reacts preferentially with C-H bonds and the excitation is reversible when no covalent bond was formed [23]. In this context, using pBzpa we could successfully confirm the crosslink product observed with pAzpa (Figure 3B). This result shows that the formation of the crosslinked product was independent of the type of photoreactive amino acid used to form a covalent bond between Aha1 I64X and an interacting protein in vivo.

For all experiments, mutant Aha1 variants were tagged using a V5/His6-tag at the C-terminus. It has already been reported that proteins containing His6-tags may differ from their wild-type counterparts in dimerization properties [35], therefore we checked whether crosslink product formation is depending on the His6-tag. In this context we expressed the wild-type Aha1, Aha1 R59X, Aha1 V63X and Aha1 I64X either with the V5-, HA- or Flag-tag using the same expression vector and linker sequence between the Aha1 and the respective tag. Using these constructs, crosslink experiments revealed that the specific type of C-terminal tag had no influence on the formation of the observed crosslink product (Figure S5). For Aha1 R59X and Aha1 I64X the crosslink product could be reproduced independent of the tag, whereas no crosslink product formation was observed for wild-type Aha1 and Aha1 V63X that were used as negative control.

Identification of the Aha1 interacting partner

The interaction of Aha1 with Hsp90 has already been demonstrated with various methods like yeast two-hybrid assay or co-immunoprecipitation [27], [36]. Moreover, this interaction is also structurally well characterized by crystal structures [28], [29]. Based on such a crystal structure we expected to capture Hsp90 by a covalent crosslink through the incorporation of pAzpa at one of the positions 59–66 in Aha1. Although the apparent molecular weight of crosslinked proteins are difficult to predict, this heterodimer should have a size of approximately 120 kDa which can be deduced from the individual molecular masses of Hsp82 (81 kDa) and Aha1 (39 kDa). Instead, we found that the crosslink product has an apparent molecular mass of 100 kDa. To test whether Hsp90 was the interaction partner of Aha1 we used Western blot analysis using anti-Hsp90 antibodies to examine whether Hsp90 is part of the crosslink product. Surprisingly, it was not possible to detect any crosslink product with two different anti-Hsp90 antibodies although the Hsp90 monomer gave a clear and strong signal (Figure 4B). Since Hsp90 was first described as a heat shock protein [31] and the expression of both proteins increase under stress conditions like elevated temperatures [37], we also cultivated Aha1 V63X and Aha1I64X strains at 21°C in galactose medium for 24 hours followed by a heat shock at 37°C for 20 min for a fraction of the culture. Afterwards, both 21°C and 37°C cultures were exposed to UV light (365 nm). Under these conditions no band in addition to the Aha1 monomer and the already observed crosslink product could be detected using an anti-V5 antibody (Figure 4A). Again, analysis with an anti-Hsp90 antibody solely showed the signal for the Hsp90 monomer, but no crosslink product at 100 kDa (Figure 4B). These experiments indicate that the crosslinked dimer does not depend on temperature and that Hsp90 could not be found covalently associated to Aha1 variants.

Figure 4. Crosslink product formation is not dependent on temperature.

A. Successful crosslink product formation could be observed both at 21 and 37 degree. No other crosslinks could be detected using an anti-V5 antibody. B. Identical samples as in A were analyzed using anti-Hsp90 antibody. No additional crosslink product band above the Hsp90 signal was detectable.

As our immunological data demonstrate that Hsp90 most likely is not the interacting partner in the covalently crosslinked protein dimer, we therefore immunoprecipitated in a next step the crosslink product in sufficient yields for analysis by mass spectrometry (Figure 5A). Following separation by SDS-PAGE and in gel digest of the cut out band of the crosslink product we found that almost all dominant peaks except for 905.69 could clearly be assigned to Aha1 (highlighted in grey), with about 81% of the Aha1 protein sequence including the C-terminal tag was covered (Figure S6). No further protein in the sample in addition to Aha1 with a significant Probability Based Mowse Score could be detected. As another covalently bound protein had to be present in the sample in stoichiometric amounts, the fact that no other protein could be detected strongly suggests a homodimerization of Aha1 with itself. The assumption that a homodimer was covalently crosslinked is supported by the apparent molecular weight which is twice as big as of a single Aha1 monomer (regarding the apparent migration behavior in SDS-PAGE). In good agreement to a putative homodimer we could also demonstrate by two-dimensional (2D) gel electrophoresis, that the homodimer shows exactly the same isoelectric points compared to the monomer (Figure S7). To confirm this homodimer we also tagged an endogenously expressed Aha1 with a C-terminal HA tag. Cells simultaneously expressing the constitutively expressed Aha1-HA as well as galactose-induced Aha1 R59X containing a V5 epitope were exposed to UV light. The corresponding V5-immunoprecipitated dimer could be detected by Western blot using the anti-HA and anti-V5 antibody (Figure 5B). No dimer was detected upon immunoprecipitation with wild type V5-tagged Aha1. This result confirms the crosslink product as a homodimer consisting of two covalently crosslinked Aha1 monomers. In additional experiments we also found that crosslink product formation was not due to aggregation of misfolded Aha1 proteins within the cell as most of the crosslinked product was found in the supernatant of high speed centrifugation representing the soluble fraction (Figure S8A). Crosslink formation also was unlikely to be co-translationally generated at poly-ribosomes as inhibition of translation using cycloheximide for different periods of times prior to UV-irradiation still results in the formation of the specific crosslink product (Figure S8B).

Figure 5. Identification of the Aha1 cross-linked interaction partner.

A. Tryptic fragmentation of the crosslinked product band that was cut out from SDS-PAGE, revealed peptides only matching to Aha1. Mass peaks that could be unambiguously assigned to Aha1 protein are highlighted in grey. No additional proteins could be detected using MASCOT's “Probability Based MOWSE Score”, indicating that the crosslink product represents a homodimer consisting of two Aha1 proteins. B. Endogenous Aha1 was fused to a HA-tag at its C-terminus and simultaneously expressed with the pAzpa-containing Aha1 mutant (59) or wild-type Aha1 (wt) fused to a V5-tag. Following irradiation with UV light Aha1-V5 was immunoprecipitated using an anti-V5 antibody. The corresponding eluates (E) were analyzed using anti-V5 and anti-HA antibodies. A crosslink product generated by the Aha1 mutant with pAzpa at the position 59 could be detected by both antibodies.


The study of protein-protein interactions by using position-specific, incorporated photo-cross-linkers such as the two non-canonical amino p-azido-L-phenylalanine or p-benzoyl-L-phenylalanine also holds numerous advantages over unspecific chemical compounds such as formaldehyde. By position-specific incorporation of non-canonical amino acids, each region of the protein can be specifically examined for interactions, including those interactions positioned in the interior of the proteins and for this reason are not accessible for chemical agents. In addition, the rapid reaction kinetic after induction with UV light permits the capture of transient and weak interactions, thereby minimizing false-positive results. Importantly, the replacement of only one amino acid is the smallest modification possible in a protein.

For this work we applied the expanded genetic code to study protein-protein interactions in S. cerevisiae using full length proteins. In this context the non-canonical amino acid pAzpa was incorporated at defined positions in the cochaperone Aha1. Aha1 was selected as a model protein because of its well characterized and proven interaction to Hsp90 by yeast two-hybrid [27], [38], co-immunoprecipitation [27], [36], multidimensional NMR technique [28] and crystallisation [29]. Depending on addition of pAzpa to the medium, we were able to incorporate the non-canonical amino acid at each of the selected positions. In contrast, recently Nehring et al. showed that they were not able to suppress an amber stop codon with pAzpa in S. cerevisiae [39]. This finding is very surprising as by using the same orthogonal pair as Nehring et al. that has been initially introduced by the group of Schultz we have expressed different proteins having incorporated the non-canonical amino acid pAzpa in S. cerevisiae strain YPH501. In addition, we also used the commercially available strain INVsc1 mentioned in this study in experiments to successfully express full length Gal4 with pAzpa at different positions. We cannot explain the lack of incorporation of pAzpa into proteins in S. cerevisiae found by Nehring et al., but would like to point out that the concept of an expanded genetic code to incorporate pAzpa and pBzpa into proteins in S. cerevisiae in vivo in fact is feasible.

Prior to carrying out photo-cross-link experiments we first confirmed the preservation of the interaction between the Aha1 variants and Hsp90 by native co-immunoprecipitation. This control was crucial as non-canonical amino acid or a fused tag may change the interaction behavior of a protein. Interestingly, we were able to generate a covalent crosslink including the positions described to be involved in the core interaction between Aha1 and Hsp90 (64 and 66) [29]. We were surprised to observe a crosslinked Aha1 homodimer as we clearly expected to find a heterodimer consisting of Aha1 and Hsp90, because the interaction interface was previously well characterized by a crystal structure [29] and confirmed by a multidimensional NMR technique [28]. However, we do not at all rule out an interaction of Aha1 to Hsp90 as we still find this interaction by native co-immunoprecipitation. It seems reasonable to speculate that an additional interface might be also probable for the interaction of both proteins under these experimental conditions in vivo. In general, the fact that in vivo photo-cross-link results do not necessarily agree with in vitro findings is in line with findings of other groups [40], for example. In this study, we have successfully demonstrated the applicability of the non-canonical amino acid p-azido-L-phenylalanine in S. cerevisiae to investigate protein-protein interactions in their natural context using the expanded genetic code. We found that an Aha1 domain which has been described to be implicated in Hsp90 binding in vitro was involved in homo-dimerization in vivo. These results therefore highlight the need for in vivo techniques for protein interaction analysis.

Materials and Methods

Strains and Materials

S. cerevisiae strain YPH501 (MATa/α ura3–52/ura3–52 lys2–801amber/lys2–801amber ade2–101ochre/ade2–101ochre trp1–Δ63/trp1–Δ63 his3–Δ200/his3–Δ200 leu2–Δ1/leu2–Δ1; Agilent Technologies) and E. coli strain DH5α (F-, endA1, hsdR17 (rk-, mk-), supE44, thi-1, recA1, gyrA96, relA1, Δ(argF-lac)U169, λ-, φ80dlacZΔM15) were used in this study. The non-canonical amino acids pAzpa and pBzpa were purchased from Bachem (Weil am Rhein, Germany). Unless otherwise indicated chemicals were from Roth (Karlsruhe, Germany) or Sigma-Aldrich (Taufkirchen, Germany). All enzymes were purchased from New England Biolabs (Frankfurt/Main, Germany). The monoclonal mouse anti-V5 antibody, the monoclonal mouse anti-Hsp90 antibody and the polyclonal rabbit anti-HA antibody were purchased from Acris (Herford, Germany). Horseradish peroxidase-conjugated sheep anti-mouse IgG and goat anti-rabbit IgG was from GE Healthcare (Freiburg, Germany). Primers used in this study are listed in Table S1.

Plasmid construction and site-directed mutagenesis

The endogenous AHA1 sequence was amplified using primers AHA1_BamHI and AHA1_XbaI containing cleavage sites for BamHI or XbaI at their 5′-ends. The PCR fragment was digested simultaneously with BamHI and XbaI subsequently cloned into the BamHI and XbaI sites of the expression vector pYES2/CT (Invitrogen). The wild-type AHA1 gene in the vector was mutagenized using the Phusion site-directed mutagenesis protocol (Thermo Scientific), to generate a series of clones with an amber stop codon at positions 59–66 (Table S1). The correct sequences of the corresponding plasmids (Table S3) were verified by sequencing.

S. cerevisiae transformation

Transformation was carried out according to standard LiAc/SS carrier DNA/PEG protocols [41]. Vectors encoding the different AHA1 variants were co-transformed with the vector encoding the aminoacyl tRNA synthetase/tRNA pair (pAR3-PGK1+3SUP4-tRNA or pBR2-PGK1+3SUP4-tRNA) into S. cerevisiae strain YPH501 to create strains for photo-crosslink-experiments (Table S2). Positive clones were selected on synthetic complete medium lacking uracil and tryptophan (SC -URA - TRP; 2% glucose, 0.17% yeast nitrogen base w/o amino acid and w/o ammonium sulfate (Difco Laboratories), 0.5% ammonium sulfate, 0.01% each adenine, arginine, cysteine, leuine, lysine, threonine and 0.005% each aspartic acid, histidine, isoleucine, methionine, phenylalanine, proline, serine, tyrosine, valine).

PCR-based tagging

PCR-based tagging was carried out according to the method of Janke with several modifications [42]. The Primers S2_AHA1 and S3_AHA1 with flanking regions of homology were used to amplify the cassette from vector pYM45 for C terminal tagging (Table S1). The amplification was performed in 50 µl reaction with 1× Phusion HF buffer, 0.2 mM dNTP's, 0.5 µM each primer, 1 U of Phusion HF DNA polymerase and approximately 100 ng cassette vector. PCR was performed with an initial denaturation at 98°C (30 sec), followed by 12 cycles of 98°C (10 sec), 60°C (30 sec), 72°C (65 sec) and 18 cycles of 98°C (10 sec), 72°C (65 sec). Following gel purification (QIAquick Gel Extraction Kit) the amplicon was transformed into S. cerevisiae strain YPH501. Positive clones were selected on YPD-plates containing 200 µg/ml geneticin (G418).

In vivo photo-cross-linking and cell lysis

Individual colonies of Aha1 variants were grown at 30°C in SC medium containing 2% glucose, but lacking uracil and tryptophan up to an OD600 of approximately 2. For the expression of Aha1 cells were reinoculated to an OD600 of 1 into SC medium containing 2% galactose and 1 mM pAzpa (dissolved to 1 M in 1 M NaOH) or pBzpa (dissolved to 0.2 M in 1 M NaOH), but lacking uracil and tryptophan and were grown for 24 hours at 30°C. Afterwards cultures were irradiated for 2 h by 365 nm UV light (Bio-Link BLX 365 Crosslinker, 5×8 W bulbs). Cells from a 20 ml culture were pelleted by centrifugation. The pellet volume was estimated and equal volume of glass beads (0.25–0.5 mm) and lysis buffer (50 mM Tris-Cl pH 7.5, 200 mM NaCl, 5 mM EDTA, 1% (v/v) Triton X-100) were added to the pellet. Cells were lysed by three 5 min cycles of vortexing in the cold room. Foam was centrifuged at 16,060 g for 2 min between the vortex steps. Lysates were cleared by centrifugation for 10 min at 16.060 g and 4°C.

Separation of soluble from insoluble proteins and cycloheximide-chase assay

Aha1 I64X (2YA6,64C1) was expressed and crosslink products were formed by irradiation with UV light. Disruption was carried out using a Mixer Mill MM 200 (Retsch) with a shaking frequency of 30 s−1. The resulting cell powder was resuspended in aqueous buffer without detergent (50 mM Tris-Cl pH 7.5, 500 mM NaCl, 1 mM PMSF, 1× protease inhibitor cocktail without EDTA (Roche)). Soluble proteins were separated from the insoluble proteins by a 100,000× g centrifugation for 30 minutes. Insoluble proteins were solved in an insoluble protein buffer (50 mM Tris-Cl pH 7.5, 8 M urea, 2% SDS, 150 mM NaCl, 2 mM DTT, 1 mM PMSF, 1× protease inhibitor cocktail without EDTA (Roche)).

For translational inhibition assays using cycloheximide Aha1 I64X (2YA6,64C1) was expressed and cycloheximide (final concentration 50 µg/ml) was added to the culture prior to UV-irradiation for different periods of time.

Western blot analysis

For Western blot analysis proteins were precipitated from cell lysates according to Wessel and Flugge [43]. Protein concentration was determined by the Dc Protein Assay (Bio-Rad). Per sample 75 µg total protein was separated by 6% or 8% SDS-PAGE [44]. After electrophoresis, the proteins were blotted onto a PVDF membrane (Immobilon P with a pore size of 0.45 µm, Millipore). The proteins were probed with either monoclonal mouse anti-V5 antibody (1∶5,000), polyclonal rabbit anti-HA antibody (1∶5,000) or monoclonal mouse anti-Hsp90 antibody (1∶1,000). Detection was carried out using peroxidase coupled sheep anti-mouse antibody (1∶5,000) or peroxidase coupled goat anti-rabbit antibody (1∶5,000) and the ECL Plus Western Blotting Substrate (Pierce) using the LAS-1000 CCD camera (Fuji Photo Film).


After 24 h of Aha1 expression under the corresponding conditions, cells were harvested by centrifugation and immediately frozen in liquid nitrogen. Disruption was carried out using a Mixer Mill MM 200 (Retsch) with a shaking frequency of 30 s−1. The resulting cell powder was resuspended in 1 ml lysis buffer (20 mM Tris-Cl pH 7.5, 1× protease inhibitor cocktail without EDTA (Roche)). Cell debris was removed by centrifugation at 16,060 g for 7 min at 4°C. For each immunoprecipitation 500 µl of the supernatant was used according to the V5 tagged Protein Purification Kit protocol (MBL International Corporation). Four washing steps were performed with wash buffer (20 mM Tris-Cl pH 7.5, 1× protease inhibitor cocktail without EDTA (Roche), 100 mM NaCl, 5 mM MgCl2, 0.1% (v/v) Tween 20). Two specific elution steps were carried out using the V5 peptide.

Mass spectrometry

In order to achieve a sufficient amount of crosslink product for MS analysis, strain 2YA6,63C1 and 2YA6,64C1 were cultured in 200 ml SC-TRP-URA medium in the presence of pAzpa as already described. The cultures were split after UV irradiation in ten 20 ml fractions and cells were lysed corresponding to the already described glass bead protocol. For each immunoprecipitation 500 µl of the supernatant was used according to the V5 tagged Protein Purification Kit protocol (MBL International Corporation). The elution of the crosslink product was performed with 50 µl 4× Laemmli buffer (200 mM Tris-Cl pH 8.0, 5% (w/v) SDS, 40% (v/v) glycerol, 20% (v/v) β-mercaptoethanol, tip of bromophenol blue). The first two 50 µl eluates were used to elute the remaining eight samples. Afterwards the two 50 µl eluates, each represent five immunoprecipitations, were pooled and separated in a large format 6% SDS-PAGE (PROTEAN® II xi Cell from Bio-Rad). The gels were stained using the FOCUS-FAST Silver Kit (G-Biosciences) which is compatible to MS analysis. The corresponding crosslink product band was cut out, proteins were digested and identified by MALDI-TOF/MS according to standard protocols (TopLab (Martinsried, Germany)) [45].

Supporting Information

Figure S1.

Effects of non-canonical amino acids and the orthogonal pair on cell growth. All experiments were performed in SC medium containing glucose as a carbon source. For all experiments two controls were used without addition of NaOH (control) and the addition of the required amount of 1 M NaOH to solubilize pAzpa (dashed line). A. Growth curves of the wild-type strain YPH501 in the presence of different pAzpa concentrations. B. Growth curves of strain 2YA6,64C1 transfected with plasmids for mutant Aha1 I64X and the orthogonal pair for site-specific incorporation of pAzpa in the presence of different pAzpa concentrations. C. Growth of strain 2YA6,64C1 in medium containing different concentrations of pBzpa.


Figure S2.

Site-specific conjugation of chemical compounds using the azido-group. A. Chemoselective ligation of the triarylphosphine fluorescent dye using the Staudinger ligation reaction. Aha1 I64X (2YA6,64C1) was expressed in the presence of pAzpa, afterwards cells were disrupted and the ligation reaction was performed using whole cell lysate. Labeled Aha1 protein was immunoprecipitated with anti-V5 antibody. The immunoprecipitate (lane 6) and 50 µg (lane 3) or 100 µg (lane 4) of lysate protein were separated by the SDS-PAGE. Fluorescence was read out by using a fluorescence scanner. Wild-type Aha1 (2YA6C1) was subjected to the same labeling reaction and was used as a negative control (50 µg protein lysate = lane 1; 100 µg protein lysate = lane 2; immunoprecipitated eluate = lane 5). B. Chemoselective conjugation of a biotin molecule using the azide-alkyne cycloaddition (Click Chemistry). Aha1 I64X (2YA6,64C1) was expressed in the presence of pAzpa, afterwards cells were disrupted and Aha1 proteins were immunoprecipitated with the anti-V5 antibody. The eluate was then used for the biotin labeling procedure. Samples before (lane 3) and after (lane 4) labeling were analyzed by Western blot using streptavidin-HRP, showing that biotin was successfully linked to Aha1 at position 64. Labeled Aha1 proteins were also detected with the anti-V5 antibody (lane 6). The wild-type Aha1 (2YA6C1) was used as the negative control before (lane 1) and after (lane 2) labeling; lane 5 represents the same sample as lane 2 but analyzed using anti-V5 antibodies.


Figure S3.

Crosslink product formation depends on position, UV irradiation and the presence of the non-canonical amino acid pAzpa. Wild-type Aha1 (2YA6C1) was used as a negative control and expression of Act1 was used as loading control. Detection of the Aha1 variants was carried out with a monoclonal mouse anti-V5 antibody and the detection of Act1 using a monoclonal mouse anti-Act1 antibody. A. Positions showing crosslink product formation. B. All positions with no crosslink product formation.


Figure S4.

Time of UV irradiation and pAzpa concentration have an influence on crosslink formation. A. Strain 2YA6,64C1 was exposed for different periods of time to UV light. Significant crosslink product formation could be observed after 15 min of irradiation with UV light. Irradiation up to 120 min leads to an increased yield of the formation of the crosslinked product. B. Cells were cultivated in medium with different pAzpa concentrations. The yield of crosslink product formation correlates to the concentration of pAzpa given to the medium. No crosslink product formation was observed without pAzpa.


Figure S5.

The C-terminal tag has no effect on crosslink product formation. Independent of the C-terminal tag, crosslink product formation could be confirmed with Aha1 variant 59 and 64. A. Different Aha1 variants were tagged with the V5 epitope at the C-terminus. Aha1 I64X (2YA6,64C1) C-terminally tagged with V5 epitope and poly-histidine tag was used as control. B. Aha1 variants C-terminally tagged with the HA epitope detected with anti-HA antibodies. C. Aha1 variants C-terminally tagged with the FLAG epitope and detected with anti-FLAG antibodies.


Figure S6.

A. Sequence coverage of the Aha1 I64X protein. Protein regions which could be covered by matching peptides are highlighted in red. Position 64 is marked in green. B. Peak table showing all found masses matching to the Aha1 I64X protein sequence.


Figure S7.

Analysis of the Aha1 homodimer by 2-D electrophoresis. Aha1 I64X (2YA6,64C1) was immunoprecipitated before (left) and after irradiation (right blot) by UV light. Eluates were separated by 2-D electrophoresis and analyzed by Western blot with monoclonal mouse anti-V5 antibody. The crosslink product migrates to the same isoelectric points as the Aha1 monomer.


Figure S8.

Crosslink products are found in the soluble fraction and are not formed co-translationally at poly-ribosomes. A. Separation of soluble from insoluble proteins was performed to show that the crosslink product is not formed due to the aggregation of misfolded Aha1 proteins within the cell. Aha1 I64X (2YA6,64C1) was expressed, crosslink products were formed by irradiation with UV light and soluble proteins were separated from the insoluble proteins by a 100,000× g centrifugation. Different volumes of each fraction were analyzed by Western Blot using mouse monoclonal anti-V5 antibody. Crosslink product as well as monomer was mainly found in the soluble fraction. B. Cycloheximide-chase assay were performed to demonstrate that crosslinking does not occur co-translationally. At different time points following addition of cycloheximide cells were exposed to UV light. Crosslink products could be formed to each time point after inhibition of the translation in comparable yields.


Table S1.

Primer sequences for cloning and mutagenesis of AHA1.


Table S2.

S. cerevisiae strains generated in this study.



We are grateful to Peter G. Schultz for the kind gift of plasmids.

Author Contributions

Conceived and designed the experiments: MB AM KS. Performed the experiments: MB AM. Analyzed the data: MB AM SP KS. Contributed reagents/materials/analysis tools: SR. Wrote the paper: MB SP KS.


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