Identification of highly reactive sequences for PLP-mediated bioconjugation using a combinatorial peptide library

Article abstract of DOI:10.1021/ja105429n

Chemical reactions that facilitate the attachment of synthetic groups to proteins are useful tools for the field of chemical biology and enable the incorporation of proteins into new materials. We have previously reported a pyridoxal 5′-phosphate (PLP)-me

Full text of DOI:10.1021/ja105429n

Published on Web 11/10/2010
Identification of Highly Reactive Sequences For PLP-Mediated
Bioconjugation Using a Combinatorial Peptide Library
Leah S. Witus,† Troy Moore,† Benjamin W. Thuronyi,† Aaron P. Esser-Kahn,†
Rebecca A. Scheck,† Anthony T. Iavarone,§ and Matthew B. Francis*,†,‡
Department of Chemistry, UniVersity of California, Berkeley, California 94720-1460, United States,
Materials Sciences DiVision, Lawrence Berkeley National Laboratories, Berkeley,
California 94720-1460, United States, and QB3/Chemistry Mass Spectrometry Facility,
UniVersity of California, Berkeley, California 94720-1460, United States
Received June 21, 2010; E-mail: francis@cchem.berkeley.edu
Abstract: Chemical reactions that facilitate the attachment of synthetic groups to proteins are useful tools
for the field of chemical biology and enable the incorporation of proteins into new materials. We have
previously reported a pyridoxal 5′-phosphate (PLP)-mediated reaction that site-specifically oxidizes the
N-terminal amine of a protein to afford a ketone. This unique functional group can then be used to attach
a reagent of choice through oxime formation. Since its initial report, we have found that the N-terminal
sequence of the protein can significantly influence the overall success of this strategy. To obtain short
sequences that lead to optimal conversion levels, an efficient method for the evaluation of all possible
N-terminal amino acid combinations was needed. This was achieved by developing a generalizable
combinatorial peptide library screening platform suitable for the identification of sequences that display
high levels of reactivity toward a desired bioconjugation reaction. In the context of N-terminal transamination,
a highly reactive alanine-lysine motif emerged, which was confirmed to promote the modification of peptide
substrates with PLP. This sequence was also tested on two protein substrates, leading to substantial
increases in reactivity relative to their wild-type termini. This readily encodable tripeptide thus appears to
provide a significant improvement in the reliability with which the PLP-mediated bioconjugation reaction
can be used. This study also provides an important first example of how synthetic peptide libraries can
accelerate the discovery and optimization of protein bioconjugation strategies.
Introduction
the many instances of the same functional groups on protein
surfaces. Although this is acceptable for some applications,
Protein bioconjugates are increasingly being used as func-
tional and structural components of new materials.1 In a typical
approach, a synthetic functional group of interest is attached to
a specific amino acid side chain using one of a relatively limited
set of chemical reactions that can modify unprotected biomol-
ecules in aqueous solution.2,3 However, most strategies (such
as lysine targeting) lead to complex product mixtures due to
improved site selectivity is required to access architecturally
precise biomolecular materials. This is often achieved by
targeting cysteine residues, but there are cases in which it is
inconvenient or impossible to introduce a single copy of this
residue without sacrificing protein function. Also, a growing
number of applications (such as FRET-based sensors,4 pollutant
responsive hydrogels,5 and therapeutic delivery systems6) require
the modification of proteins in two distinct locations. While
cysteine modification may be used to install the first group,
compatible modification methods that can be used to install the
second functional group are in short supply.
† Department of Chemistry, University of California, Berkeley.
§ QB3/Chemistry Mass Spectrometry Facility, University of California,
Berkeley.
‡ Lawrence Berkeley National Laboratories.
(1) For lead examples, see: (a) Douglas, T.; Young, M. Nature 1998, 393,
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As one solution to this challenge, we have previously
reported7-9 a protein bioconjugation reaction that achieves site-
(4) Crochet, A. P.; Kabir, M.; Francis, M. B.; Paavola, C. D. Biosens.
Bioelectron. 2010, 26, 55-61.
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2008, 130, 15820–15822.
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Highly Reactive Sequences For PLP-Mediated Bioconjugation
A R T I C L E S
cysteine alkylation12 as well as C-terminal modification using
native chemical ligation (NCL).19,20
PLP-mediated bioconjugation has been used to modify a
number of different proteins in applications ranging from surface
and polymer attachment21 to the dual modification of viral coat
proteins with different chromophores for light harvesting
systems.12 Since the initial report of this method for protein
functionalization, our group has sought to explore the scope of
this reaction and to improve its reliability for new protein targets.
Our previous work has shown that the transamination reactivity
of a protein is dependent on the identity of the N-terminal
residue, as well as those in the second and third positions.9 The
terminal and internal residues were found to have a complex
synergistic effect on the overall reactivity, quickly outpacing
our ability to screen sequence candidates individually.
Based on the observation that the penultimate and antepen-
ultimate residues are significant in determining the reactivity
of peptides and proteins toward PLP-mediated N-terminal
transamination, we sought to identify the most highly reactive
sequences of amino acids from the chemical space spanning
all combinations of three N-terminal residues. To identify such
sequences, we developed a combinatorial peptide library screen-
ing platform based on a colorimetric detection of desired
reactivity, as outlined in Figure 2. Using stringent reaction
conditions to screen for the most active sequences, a highly
conserved alanine-lysine motif was identified. The improved
reactivity of this motif was verified on peptide substrates, and
the scope was explored using positional scanning experiments.
Additionally, we introduced this sequence on two proteins using
site-directed mutagenesis. In both cases, the alanine-lysine
mutants exhibited improved yields relative to the wild-type
termini. It is anticipated that this new, highly reactive motif
will serve to increase the reactivity of many other protein targets.
Figure 1. The general scheme of PLP-mediated bioconjugation. (a) In the
first step, a protein is incubated with PLP (1) under mild, aqueous conditions.
This oxidizes the N-terminus of the protein to a ketone or an aldehyde,
providing a unique functional group for further modification. (b) In the
second step, the ketone is conjugated to an alkoxyamine-bearing reagent
(2) through oxime formation. (c) The proposed mechanism begins with
Schiff base formation between the N-terminal amine and the PLP aldehyde.
Tautomerization, followed by hydrolysis, affords the keto-protein product.
specificity by targeting the N-terminus, a unique position in the
sequence. When incubated with pyridoxal 5′-phosphate (PLP),
the N-terminal amine undergoes a transamination reaction that
installs a ketone or an aldehyde in that position without
modifying lysine side chain amines.7 The unique reactivity of
the new carbonyl group relative to native side chain function-
alities allows for further conjugation to alkoxyamine-containing
probes via oxime formation10,11 (Figure 1). This technique
provides a convenient and readily scalable way to install a single
functional group in a single location and has been shown to
tolerate free cysteine residues.4,5,12
Results and Discussion
Design of a Peptide Library Screening Platform. Although
the reactivity of full-sized proteins will undoubtedly be influ-
enced by their tertiary structure, previous work9 had demon-
strated that general trends in N-terminal reactivity were con-
sistent between peptide and protein substrates. This observation
suggested that it would be possible to screen peptide libraries
to identify sequences that would retain their reactivity in the
protein context. To do this, we developed a screening platform
by adapting a number of traditional techniques used for the
construction of solid-phase combinatorial peptide libraries.22 As
our objective was to find a short genetically encodable sequence
that could be conveniently introduced through mutagenesis, we
limited our randomization to the terminal three residues, which
were followed by an invariant region that could include
purification handles or other sequences of interest in future
There are other methods of N-terminal modification,13-17
each of which may be suitable for different applications and
proteins. N-terminal tryptophan residues16 can be ligated to
aldehyde reagents via a Pictet-Spengler reaction, but it can be
difficult to obtain proteins with a tryptophan in the N-terminal
position.18 N-terminal serines and threonines can be cleaved
using sodium periodate to yield aldehyde functionalities for
further derivitization.17 However, sodium periodate may not be
compatible with some applications, such as glycoproteins and
proteins with large numbers of cysteine or methioine residues.5
PLP-mediated transamination is complementary to these other
methods of N-terminal modification and is especially useful
because of its compatibility with other protein modification
strategies. For instance, it can be used in combination with
(19) (a) Dawson, P. E.; Muir, T. W.; Clarklewis, I.; Kent, S. B. H. Science
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Chem. Soc. 2000, 122, 5421–5428.
(10) Jencks, W. P. J. Am. Chem. Soc. 1959, 81, 475–481.
(11) Rose, K. J. Am. Chem. Soc. 1994, 116, 30–33.
(12) Dedeo, M. T.; Duderstadt, K. E.; Berger, J. M.; Francis, M. B. Nano
Lett. 2010, 10, 181–186.
(20) Esser-Kahn, A. P.; Francis, M. Angew. Chem., Int. Ed. 2008, 120,
3811–3814.
(13) Tam, J. P.; Yu, Q.; Miao, Z. Biopolymers 1999, 51, 311–332.
(14) Dixon, H. B. F. J. Protein Chem. 1984, 3, 99–108.
(15) Dixon, H. B. F.; Fields, R. Methods Enzymol. 1972, 25, 409–419.
(16) Li, X.; Zhang, L.; Hall, S. E.; Tam, J. P. Tetrahedron Lett. 2000, 41,
4069–4073.
(21) (a) Christman, K. L.; Broyer, R. M.; Tolstyka, Z. P.; Maynard, H. D.
J. Mater. Chem. 2007, 17, 2021–2027. (b) Lempens, E. H. M.; Helms,
B. A.; Merkx, M.; Meijer, E. W. ChemBioChem 2009, 10, 658–662.
(c) Gao, W.; Liu, W.; Mackay, J. A.; Zalutsky, M. R.; Toone, E. J.;
Chilkoti, A. Proc. Natl. Acad. Sci. U.S.A. 2009, 106, 15231–15236.
(22) (a) Lam, K.; Lebl, M.; Krchnak, V. Chem. ReV. 1997, 97, 411–448.
(b) Lam, K. S.; Salmon, S. E.; Hersh, E. M.; Hruby, V. J.; Kazmierski,
W. M.; Knapp, R. J. Nature 1991, 354, 82–84.
(17) Geoghegan, K. F.; Stroh, J. G. Bioconjugate Chem. 1992, 3, 138–
146.
(18) Hirel, P. H.; Schmitter, M. J.; Dessen, P.; Fayat, G.; Blanquet, S. Proc.
Natl. Acad. Sci. U.S.A. 1989, 86, 8247–8251.
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Witus et al.
Figure 2. Library screening scheme. (a) The 8000-member combinatorial peptide library of the form XXXWSNAG was subjected to PLP-mediated
transamination and subsequent oxime formation with Disperse Red alkoxyamine 2a. Stringent reaction conditions were used during the PLP reaction such
that only sequences with high reactivity transaminated to form a keto group. These active sequences were colorimetrically distinguished from the others
during the next step, where the Disperse Red dye formed a covalent oxime linkage with the transaminated sequences. The library was then examined under
a microscope, and the red beads were manually removed for sequencing. (b) Each bead contained a truncation ladder in addition to the full-length peptide
that had participated in the reaction. Sequencing was performed by cleaving the peptide species from selected beads and identifying the ladder peptides using
MALDI-TOF MS. The mass differences between adjacent capped species corresponded to the amino acid in that position. Capped species were easily
identified by the unique isotope pattern of the bromine atoms. The mass of the uncapped peptide can be identified at 824 m/z, confirming the assignment.
The stuctures of the bromobenzoic acid caps 3 and 4 and the Disperse Red alkoxyamine used in these experiments are shown in (c).
studies. The resulting library included all 20 natural amino acids
in each of the three N-terminal positions, corresponding to 8000
members.
To identify beads bearing sequences with high levels of
transamination activity, we developed a colorimetric detection
method for the ketone and aldehyde products (Figure 2a).
Peptides that yielded these functional groups were easily
distinguished from those that did not upon subsequent treatment
with a Disperse Red alkoxyamine (2a) to form a bright red
oxime product (the synthesis of the Disperse Red alkoxyamine
is described in the Supporting Information). The oxime forma-
tion was performed over 3 h using 10 mM Disperse Red
alkoxyamine in DMF. Washing to remove unbound Disperse
Red led to a clear contrast between beads with and without
covalent modification (Supporting Information Figure S2).
Spatial separation of the library components on a Petri dish
allowed visual detection and manual removal of the red beads
for determination of the corresponding sequences.
The library was synthesized on resin beads using a split-and-
pool technique.22 Additional steps were performed after the
coupling of each variable position to cap a portion of the
growing chain to facilitate sequencing by mass spectrometry,
as described below. A five-amino acid base sequence, WSNAG,
was synthesized before the variable positions to provide the
library members with enough mass to separate their signals from
matrix noise peaks during MALDI-TOF MS analysis. Standard
Fmoc solid-phase peptide chemistry was used during the
synthesis, which was based on Tentagel resin to allow aqueous
screening conditions to be performed while the peptides were
still attached to the beads.
A key step of the library screening scheme was the develop-
ment of a simple and rapid method of determining the sequence
on active beads. To this end, we created a sequencing technique
based on a built-in truncation ladder.23 As compared to de noVo
sequencing based on tandem MS/MS fragmentation data, this
approach allowed for facile identification of the peptide sequence
using only intact ions. To create a truncation ladder, a small
portion (<10%) of the growing peptide on each bead was capped
with bromobenzoic acid (3) during synthesis of the variable
positions. Once cleaved, the unique isotope patterns of these
truncated species enabled their unambiguous identification,
allowing the sequence on each bead to be determined by simple
calculation of the mass differences between the molecular ions
(Figure 2b). Additionally, we were able to differentiate between
isobaric amino acids (isoleucine and leucine) and nearly isobaric
amino acids (glutamine and lysine) by capping one of each pair
with methylbromobenzoic acid (4) during the synthesis. Sup-
porting Information Figure S1 shows the analysis of a repre-
sentative library member, in which the relative amounts of
peptide and capped species on an individual bead can be seen.
Screening for Highly Reactive N-Terminal Sequences. The
standard conditions reported for PLP-mediated transamination
of peptide substrates are 10 mM PLP in 50 mM pH 6.5
phosphate buffer for 18 h at room temperature. When the library
was subjected to these reaction conditions (Figure 3a), the
majority of the library members were modified by the
alkoxyamine dye. As expected, varying degrees of conversion
for different sequences could be observed in the various shades
of red ranging from nearly colorless to light orange to deep
red. This visual representation of reactivity corresponded well
with our previous experience of PLP-mediated bioconjugation
on protein substrates. To access sequences with greater than
average reactivity, we next applied more stringent reaction
conditions by lowering the concentration of PLP. Subjecting
the library to 1 mM PLP resulted in fewer and lighter red beads
(Figure 3b). When the library was treated with 100 µM PLP, a
stark contrast in relative reactivity was seen: almost all of the
beads were colorless except for a very small number (∼1 in
300) that were bright red (Figure 3c). The library was screened
multiple times with these conditions using approximately 24
mg of resin, which corresponded to 24 000 beads (three times
(23) Youngquist, R. S.; Fuentes, G. R.; Lacey, M. P.; Keough, T. J. Am.
Chem. Soc. 1995, 117, 3900–3906.
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Highly Reactive Sequences For PLP-Mediated Bioconjugation
A R T I C L E S
Figure 4. Analogues of the reactive alanine-lysine motif identified during
library screening were synthesized to verify the reactivity of this sequence.
AKT was compared to LKT to confirm the importance of alanine as the
first residue, and AET was used to probe the role of a positive charge in
the second position. At 0.1 mM PLP, the concentration of library screening,
AKT showed a significantly higher yield than the other sequences. AKT
also resulted in notably improved yields at higher concentrations of PLP.
Figure 3. Visual evaluation of the library at different screening conditions,
including sequences identified from a 100 µM PLP reaction. (a) When
incubated with 10 mM PLP, the majority of the library members turned
red, confirming that at standard reaction conditions many sequences exhibit
at least some degree of conversion. (b) Using 1 mM PLP, fewer library
members turned red, and most showed a lighter color. (c) Using only 100
µM PLP, most of the sequences showed no conversion (as evidenced by
the colorless beads), but a small number of red beads were still identified.
(d) The sequences corresponding to the red beads at 100 µM PLP revealed
AXK and AKX as the predominant N-terminal motifs.
tryptophan fluorescence ratios of the products were also
compared in some cases. Similar results were obtained.
Under conditions identical to those that were used to screen
the library (100 µM PLP, 18 h, room temperature), the AKT
peptide provided a 30% yield of oxime product (Figure 4).
Peptides containing only one of these components (i.e., AET-
and LKT-WSNAG) were found to be unreactive under these
conditions, confirming the synergistic effect of the Ala-Lys
combination. At higher PLP concentrations, the yield of oxime
product increased for all three peptides, with the AKT sequence
consistently producing higher reactivity. The mechanism of the
transamination reaction almost certainly involves reversible
imine formation as the first step, followed by tautomerization.
It is likely that the positive charge of the lysine residue serves
to recruit the PLP molecule through interactions with the
phosphate group, thus increasing the value of K1 in Figure 1b.
The origin of the beneficial alanine effect is less clear, as this
residue could influence the equilibrium position of the tau-
tomerization step (K2) as well as encourage hydrolysis and/or
oxime formation.
the library size, a ratio that has been calculated to represent
95% of the members24).
The sequences that were identified after selection and
sequencing of the red beads are listed in Figure 3d. These
sequences showed a high degree of consensus and were
categorized by a few convergent patterns. The preferred
N-terminal amino acid showed a striking preference for alanine,
which was typically followed by a positively charged amino
acid in the second or third position, with lysine being more
common than arginine. There were also several lysine terminal
sequences, as well as other sequences that did not match this
motif. The prevalence of N-terminal alanine fit our previous
observations of this reaction,9 but the benefits of the adjacent
positive charge had not been formally observed. Interestingly,
our previous reactivity screens also contained a lysine residue
in position 2. This was included for the purpose of increased
solubility and to check for lysine modification in addition to
N-terminal transamination. Although it was not modified
directly, it now seems that this residue was more than an
innocent bystander in these reactions.
Verification of Identified Consensus Sequences. Although the
red color of the beads identified during library screening was
indicative of the oxime product, the MALDI-TOF mass spectra
of the peptide mixtures cleaved from individual beads were not
sufficient for quantification of the reaction yield. To get a more
detailed understanding of the product distribution of the alanine-
positive charge motif, we resynthesized the AKTWSNAG
sequence. Upon subjecting beads (10 mg) bearing this peptide
to identical transamination conditions, they were visually found
to react with the Disperse Red alkoxyamine much as they had
during the library screen. Quantification of the reaction conver-
sion was achieved by reacting the N-terminal ketones with
benzylalkoxyamine (250 mM in H2O, 3 h), as we found that
the Disperse Red oxime tag suppressed ionization. After analysis
by LC-QTOF MS, integration of the extracted ion chromato-
grams of the reaction products was used to obtain the relative
yields of each species.9 As confirmation of these values, the
Positional Scanning. A positional scanning experiment was
performed to determine the ideal position of lysine (in either
the second or the third position), and to identify any residues
that might suppress the reactivity of the motif, which would be
important to avoid when using this motif as a tag sequence on
proteins. We synthesized 38 octapeptides, in which the three
N-terminal residues were of the form AXK or AKX. The
identity of X was varied to include each of the 20 natural amino
acids, with the exception of cysteine. After subjecting these
peptides to standard PLP transamination conditions (10 mM,
18 h), we found that all of the sequences with alanine in the
first position and lysine in the second or third position gave
relatively high yields of oxime product (Figure 5). Despite some
variation in yield, the lowest observed was still above 50%,
and no residues were found to quench the reactivity of the motif
substantially. The most apparent trend was a slight preference
for lysine in the second position over the third position. Because
alanine-lysine-threonine had one of the highest yields of the
synthesized peptides and it occurred multiple times in the library
screen, we chose this specific sequence to pursue as an optimized
protein modification tag.
(24) Burgess, K.; Liaw, A. I.; Wang, N. J. Med. Chem. 1994, 37, 2985–
2987.
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Figure 5. Positional scanning was performed to explore the scope of the
AKX and AXK motifs. The total oxime yield after reaction with standard
PLP conditions (10 mM, 18 h) was determined for 38 peptides with varied
amino acids in the X positions (all natural amino acids except cysteine
were included). Although high yields were seen in all cases, peptides with
lysine in the second position consistently provided higher conversion.
Application to Protein Substrates. Protein modification reac-
tions are typically performed at substrate concentrations that
are significantly lower than those used for peptide modification.
Although we have not yet determined the rate law for the
transamination reaction, it is reasonable to expect it to depend
on the concentration of both PLP and the N-terminal group.
Correspondingly, the low concentration of a protein should
require a higher PLP concentration to compensate and will be
particularly sensitive to the magnitude of K1 in Figure 1b. To
determine if the alanine-lysine-threoine motif would improve
the reactivity of proteins through this effect, we installed it on
two different substrates: Green Fluorescent Protein (GFP) and
the Type III “Antifreeze” Protein (AFP).25 Figure 6a,b indicates
the locations of the new sequences on the protein surfaces. On
AFP, the AKT motif was a two-residue extension of the wild-
type N-terminus, and on GFP the AKT residues replaced the
wild-type sequence with no extension of the N-terminus. The
wild-type N-terminal sequence of GFP (MVS) has minimal
reactivity toward PLP from room temperature to 37 °C,20 and
the wild-type AFP has fair-to-good reactivity. After expression
and purification, the wild-type and AKT variants of these
proteins were incubated with PLP at 37 °C, concentrated to
remove excess PLP after the reaction, and then subjected to
benzylalkoxyamine (25 mM in 25 mM phosphate buffer pH
6.5, 18 h) to allow quantification of the product distribution
using mass spectrometry.
Wild-type AFP showed intermediate levels of oxime product
formation, which followed the expectations of a GNQ N-
terminal sequence. However, the AKT mutant outperformed the
wild type under every set of reaction conditions screened
(including variation of the concentration of PLP and the reaction
time), as shown in Figure 6c and d. Upon inspection of the
product distribution for the AKT-terminal mutant (Figure 6e),
we observed a significant amount of covalent PLP addition to
the N-terminus, which corresponded by mass to an aldol addition
of PLP to the introduced ketone group (Supporting Information
Figure S3). However, the aldol addition of PLP did not preclude
oxime formation, as the green portions of the bars correspond
to the reaction of the PLP adduct with the alkoxyamine agents.
Thus, in many applications where the goal is simply to ligate
the target protein to another material through oxime formation,
the PLP addition byproduct may be innocuous.
Figure 6. The performance of wild-type and AKT-terminal sequences were
compared for the transamination of two protein substrates. The positions of the
new termini are shown for (a) an “Antifreeze” Protein (AFP) and (b) GFP. The
Ala residue is in red, and the Lys-Thr portion is in yellow. (c) The transamination
of the AFP mutant showed that the AKT sequence outperformed the wild-type
terminus (GNQ) at every time point analyzed. (d) The AKT-terminal AFP also
outperformed the wild-type sequence at different concentrations of PLP. (e) The
product distribution of the AKT-terminal AFP mutant shows that maximum oxime
yield (blue plus green) and minimum PLP adduct (green plus pink) could be
achieved by optimizing the reaction conditions. The dotted line marks the highest
total oxime yield achieved, demonstrating that the strategies that decreased byproduct
formation did not sacrifice overall yield. (f) Using the strategy of a high concentration
of PLP for a short reaction time, conditions were found that gave a high oxime
yield with minimal byproducts for AKT-terminal GFP in only 90 min. The wild-
type GFP mutant achieved no modification under the same conditions, highlighting
the enhanced reactivity conferred by the AKT sequence.
As would be expected for a bimolecular reaction, we observed
that the yield of PLP adduct increased with the same parameters
as transamination (i.e., higher concentrations of PLP and
increased reaction times). Because the PLP adduct likely forms
after the transamination has taken place (Supporting Information
(25) Esser-Kahn, A. P.; Trang, V.; Francis, M. B. J. Am. Chem. Soc. 2010,
132, 13264-13269.
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A R T I C L E S
Figure S4), we hypothesized that a balance of these two reaction
conditions might minimize PLP adduct formation without
sacrificing the total oxime yield. For AFP, using a lower
concentration of PLP for the full reaction time (5 mM for 18 h)
or using the standard concentration for a shorter time (10 mM
for 9 h) resulted in decreased amounts of PLP adduct (green
bar, Figure 6e) while preserving the total amount of oxime yield,
shown as a dotted line. Therefore, to minimize the PLP adduct
byproduct, it is recommended that lower concentrations of PLP
be used for longer reaction times, or that higher concentrations
of PLP be used for shorter incubation periods. In practice, the
optimal balance varies somewhat for each protein substrate, and,
like most other organic reactions, a preliminary screen of the
reaction variables is recommended.
for the introduction of a second functional group will benefit
many applications.
Conclusion
The proteins AFP and GFP demonstrate that mutating the
N-terminal sequence of a protein to AKT can increase reactivity
toward PLP-mediated bioconjugation, and thus these results
serve to validate our combinatorial peptide library screening
process. We have also identified reaction conditions for AKT-
terminal proteins that maximize yield and purity. We anticipate
that the development of this encodable motif will be of interest
to those in the chemical biology and biomolecular materials
communities who wish to apply this mild, site-specific tran-
samination reaction to their own protein substrates. On the basis
of the success of these studies, we are continuing to use this
combinatorial library screening platform to accelerate the
discovery and optimization of new bioconjuation reactions. In
particular, we are using this platform to identify new transami-
nation agents that have a reduced tendency to form addition
products.
Applying these strategies for maximizing oxime yield with
minimal PLP addition byproduct led to striking results for AKT-
terminal GFP. Using the high concentration of PLP/short
reaction time strategy, we observed over 90% yield of oxime
product with negligible amounts of byproducts by using 100
mM PLP for 90 min (Figure 6f). Under the same conditions,
wild-type GFP (N-terminal sequence: MVS) provided no
conversion, highlighting the importance of the AKT sequence
for achieving increased reactivity. Screening of the full peptide
library with these reaction conditions resulted in high reactivity
for a number of beads, with too many being observed to allow
meaningful sequencing. The product distributions of AKT-
terminal GFP under other reaction conditions are shown in
Supporting Information Figure S5. As GFP is commonly fused
to protein domains to allow visualization using fluorescence,
we anticipate that the availability of a fast and reliable method
Acknowledgment. This work was generously supported by the
NIH (R01 GM072700). L.S.W. was supported by a predoctoral
fellowship from the NSF. L.S.W., B.W.T., and A.P.E.-K. were
supported by the Berkeley Chemical Biology Graduate Program
(NRSA Training Grant 1 T32 GMO66698 and Genentech Founda-
tion Fellowship (B.W.T.).
Supporting Information Available: Full experimental details
and additional characterization spectra. This material is available
free of charge via the Internet at http://pubs.acs.org.
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