The characterization of the enzyme mutant forms L85A, L276A and L85A⁄ L276A under native conditions indicated that the stability of the cluster is essential for the correct quaternary as
Trang 1Escherichia coli serine hydroxymethyltransferase – the role
of evolutionarily conserved hydrophobic contacts
Rita Florio1, Roberta Chiaraluce1, Valerio Consalvi1, Alessandro Paiardini1, Bruno Catacchio1,2, Francesco Bossa1,3and Roberto Contestabile1
1 Dipartimento di Scienze Biochimiche ‘A Rossi Fanelli’, ‘Sapienza’ Universita` di Roma, Italy
2 CNR, Istituto di Biologia e Patologia Molecolari, ‘Sapienza’ Universita` di Roma, Italy
3 Centro di Eccellenza di Biologia e Medicina Molecolare (BEMM), ‘Sapienza’ Universita` di Roma, Italy
Introduction
Pyridoxal 5¢-phosphate (PLP)-dependent enzymes
comprise a vast and highly diversified group of
cata-lysts, whose action is required in a large number of
cellular processes It is generally accepted that PLP-dependent enzymes originated very early on in evolution, before the three biological kingdoms
Keywords
cofactor binding site; conserved
hydrophobic contacts; pyridoxal phosphate;
serine hydroxymethyltransferase;
urea-induced denaturation
Correspondence
R Contestabile, Dipartimento di Scienze
Biochimiche, ‘Sapienza’ Universita` di Roma,
Piazzale Aldo Moro 5, 00185, Roma, Italy
Fax: +39 0649917566
Tel: +39 0649917569
E-mail: roberto.contestabile@uniroma1.it
Website: http://w3.uniroma1.it/bio_chem/
sito_biochimica/EN/index.html
(Received 3 September 2009, revised 12
October 2009, accepted 16 October 2009)
doi:10.1111/j.1742-4658.2009.07442.x
According to their fold, pyridoxal 5¢-phosphate-dependent enzymes are grouped into five superfamilies Fold Type I easily comprises the largest and most investigated group The enzymes of this group have very similar 3D structures Remarkably, the location of the cofactor in the active site, between the two domains that form a single subunit, is almost identical in all members of the group Nonetheless, Fold Type I enzymes show very lit-tle sequence identity, raising the question as to which structural features determine the common fold An important fold determinant appears to be the presence of three evolutionarily conserved clusters of hydrophobic con-tacts A previous investigation, which used Escherichia coli serine hydrox-ymethyltransferase, a well characterized Fold Type I member, demonstrated the involvement of one of these clusters in the stability of the quaternary structure The present study focuses on the role of the same cluster in the stability of the cofactor binding site The investigation was carried out by equilibrium denaturation experiments on serine hydroxymethyltransferase forms in which the hydrophobic contact area of the cluster under study was reduced by site-directed mutagenesis The results obtained show that the mutations clearly affected the process of pyridoxal 5¢-phosphate dissociation induced by urea, reducing the stability of the cofactor binding site We sug-gest that the third cluster promotes the formation of a bridging structural region that stabilizes the overall protein structure by connecting the two domains, shaping the cofactor binding site and participating in the forma-tion of the quaternary structure
Structured digital abstract
l MINT-7293394 , MINT-7293405 , MINT-7293418 : eSHMT (uniprotkb: P0A825 ) and eSHMT (uniprotkb: P0A825 ) bind ( MI:0407 ) by cosedimentation in solution ( MI:0028 )
Abbreviations
CHCs, conserved hydrophobic contacts; eSHMT, Escherichia coli serine hydroxymethyltransferase; PLP, pyridoxal 5¢-phosphate.
Trang 2diverged, from different protein ancestors that
gener-ated five independent families, corresponding to as
many different Fold Types [1,2] The Fold Type I,
or aspartate aminotransferase family, is the largest,
functionally most diverse and best characterized Its
members are made of dimers or multiple of dimers,
whose subunits are formed by a large domain and a
small domain Despite the poor sequence similarity
among many Fold Type I enzymes, all members of
the family share the same basic protein architecture,
and are assembled with 17 structurally conserved
regions that form the heart of the domains [3] The
presence of three clusters of evolutionarily conserved
hydrophobic contacts (CHCs; Fig 1A) appears to be
one important structural feature determining the
native fold of Fold Type I enzymes [3] Although
two of these clusters are located in the central cores
of the domains and presumably stabilize their
scaf-fold, the role of the third cluster is much less clear
This cluster forms a hinge between two conserved
a-helices (which correspond to two structurally
con-served regions), located respectively at the beginning
and at the end of the large domain Examination of
the contact network shows that, in this cluster, the
CHCs lie along one side of each helix, forming a
buried spine at positions i, i + 4 and i + 7
In a previous study investigating dimeric Escherichia
coli serine hydroxymethyltransferase (eSHMT; EC
2.1.2.1), a well characterized Fold Type I member, we
reported a site-directed mutagenesis study in which the
third cluster of CHCs was destabilized, reducing its
hydrophobic contact area [4] The characterization of
the enzyme mutant forms (L85A, L276A and
L85A⁄ L276A) under native conditions indicated that
the stability of the cluster is essential for the correct
quaternary assembly of the enzyme and is increased
by the binding of PLP and substrates Indeed, the
two helices that form the cluster interact with the
N-terminal a-helix of the other subunit in the dimer
and are contiguous with two polypeptide loops, which,
in all Fold Type I enzymes, mediate the interactions
between the subunits and are involved in cofactor
binding, substrate binding and catalysis (Fig 1) On
the other hand, the mutations did not affect either the
capability to bind the cofactor or the catalytic activity
of the enzyme The monomeric form of the enzyme
(resulting from the double L85A⁄ L276A mutation)
binds PLP with comparable affinity with respect to the
dimeric wild-type form, suggesting that the subunit
structure of the monomer is more or less the same as
that in the dimer
By contrast with the CHCs located in the core of
the large and small domains, the third hydrophobic
A
B
Fig 1 (A) Cartoon representation of the crystal structure of eSHMT,
a Fold Type I enzyme, showing the residues involved in CHCs as spheres Subunits of eSHMT ternary complex with glycine and 5-for-myl-tetrahydropteroylglutamate (Protein Data Bank code: 1dfo) are represented in cyan and salmon Residues forming CHCs are shown only in one subunit The residues of the clusters located in the large and small domains are shown in magenta and orange, respectively The residues forming the third cluster are shown in red The PLP–Gly complex is represented by yellow sticks, with the phosphorus atom depicted in orange, the oxygen atoms in red and the nitrogen atoms
in blue The helices forming the third cluster interact with the N-ter-minal helix of the other subunit in the dimer (shown in blue) Two polypeptide loops (in green), which are contiguous with the helices
of the third cluster of CHCs, contribute residues that interact, at the active site of the other subunit, with PLP and substrates (B) Mono-meric structure of eSHMT Only the residues involved in the forma-tion of the third CHCs are shown as spheres and the mutated residues are indicated by arrows The N-terminal tail (residues 1–61)
of the protein is coloured in orange, the large domain (residues 62– 211) in salmon, the interdomain segment (residues 212–279) in green and the small domain in blue (for details, see Discussion).
Trang 3cluster is not directly involved in the proper
position-ing or stabilization of the active site or PLP-bindposition-ing
residues Its location rather suggests a role in bridging
different structural regions of the protein in order to
stabilize its native overall fold The present study
investigated the role of the third cluster of CHCs with
respect to the structural stability of the PLP-binding
site by means of urea-induced denaturation
experi-ments on eSHMT L85A, L276A and L85A⁄ L276A
mutants These mutations were carried out to reduce
the hydrophobic contact area in the cluster Leu276 is
the most conserved residue in the cluster, with its
posi-tion being almost invariably occupied by a leucine
resi-due in Fold Type I enzymes [3] Leu85 was chosen
because this residue shows the largest contact area
with Leu276
Results
The structural stability of holo-eSHMT wild-type and
mutant forms was investigated by performing
equilib-rium unfolding experiments, using urea as denaturing
agent The structural changes of the active site and
overall protein induced by urea were monitored by
measuring catalytic activity, the fraction of covalently
bound cofactor, intrinsic fluorescence emission, far-UV
CD and the sedimentation coefficient
The reversibility of the unfolding process was
ana-lyzed by measuring the activity that denatured eSHMT
samples (23 lm in 8 m urea at 20C) were able to
recover after 4 h, subsequent to a ten-fold dilution
with buffer at 20C In agreement with a previous
study [5], complete enzyme activity was recovered after
refolding In this respect, comparable results were
obtained with all mutant forms
Activity and internal aldimine measurements
Enzyme samples (2.3 lm) were incubated with
increas-ing urea concentrations in 50 mm NaHepes buffer (pH
7.2), containing 200 lm dithiothreitol and 100 lm
EDTA, at 20C for 15 h The residual fractions of
catalytic activity and covalently bound cofactor
(inter-nal aldimine) were then measured and reported as a
function of denaturant concentration (Fig 2) With all
enzyme forms, the loss of internal aldimine appears to
take place according to a sigmoid process The
decrease in catalytic activity shows a more complex
behaviour At a urea concentration in the range 0–1 m,
almost half of the activity is lost, apparently as a result
of an hyperbolic process The complete loss of activity,
taking place at higher urea concentrations, appears to
follow a sigmoid course In 1 m urea, almost all the
cofactor is bound to the enzyme as internal aldimine, indicating that the loss of activity does not result from the denaturation of the active site These observations suggest that urea might act as an enzyme inhibitor Indeed, experiments in which the kinetic parameters of the catalyzed reaction were determined in the absence
or presence of 0.25, 0.50, 0.75 and 1 m urea clearly demonstrated that urea is responsible for a mixed-type
Fig 2 Dependence of catalytic activity and PLP covalent binding
to eSHMT on the urea concentration The fractions (f) of retained catalytic activity (open symbols) and internal aldimine (closed sym-bols) were measured as a function of the urea concentration The reaction catalyzed by eSHMT was the aldol cleavage of L -threo-3-phenylserine into glycine and benzaldehyde The profiles obtained with the L85A (triangles), L276A (squares) and L85A ⁄ L276A (dia-monds) mutants are compared in each panel with the profiles obtained with the wild-type enzyme (circles) The lines through the experimental points (dashed lines for wild-type and continuous lines for mutant enzymes) are those obtained from the global nonlinear least squares fitting of internal aldimine and activity data to Eqns (1,2).
Trang 4inhibition The inhibitory effect of urea on catalytic
activity has been also reported for other enzymes and
is well documented in the literature [6,7]
Figure 2 shows that the denaturation profiles of the
L85A and L85A⁄ L276A mutants are shifted toward
lower urea concentrations with respect to those of the
wild-type and L276A enzymes To quantify this shift,
the internal aldimine and activity data of each enzyme
form were analyzed according to Eqn (1) (the equation
of a sigmoid curve) and Eqn (2) (which takes in
account both the inhibitory and denaturing effects of
urea), respectively, in a global least squares
minimiza-tion procedure in which the parameters of the sigmoid
denaturation processes contained in both equations
were shared (Fig 2) The analysis gave a good global
fit of the data and showed that the midpoints of the
sigmoid transitions coincide and, in the case of the
L85A and L85A⁄ L276A mutants, are approximately
0.3 m lower compared to the wild-type (Table1)
Although the midpoint of the L276A mutant coincides
with that of the wild-type enzyme, it is clear from the
values of n given in Table 1 that the steepness of the
sigmoid transitions is lower This indicates that the
mutation had the effect of lowering the cooperativity
of the denaturation process The same consideration
can be made for the double L85A⁄ L276A mutant
Spectroscopic measurements
Intrinsic fluorescence emission and far-UV CD
mea-surements on wild-type and mutant eSHMTs were
car-ried out on protein samples (2.3 lm) incubated with
increasing denaturant concentrations (from 0 to 7.9 m)
in 50 mm NaHepes buffer (pH 7.2), containing 200 lm
dithiothreitol and 100 lm EDTA at 20C for 15 h
(Fig 3) With the wild-type enzyme, a urea
concentra-tion rising up to 2.3 m determines the increase in
rela-tive fluorescence emission intensity (Fig 3A) Part of
this increase clearly takes place with negligible
dissoci-ation of the cofactor (from 0 to 1 m urea) and appears
to coincide with the drop of catalytic activity attribut-able to urea inhibition The further increase of fluores-cence matches the complete loss of catalytic activity and the release of the cofactor, which relieves the quenching of tryptophan fluorescence [5] As previ-ously shown, this represents the first of two steps in the denaturation mechanism of eSHMT At a urea concentration of 2.3 m, the enzyme is known to exist
in the form of a denaturation intermediate [5,8,9], which denatures completely and loses part of its fluo-rescence emission as the urea concentration is increased up to 7.9 m
The fluorescence profiles obtained with the mutant enzymes are similar in shape to that of wild-type eSHMT However, at a urea concentration in the range 0–1 m, the relative fluorescence emission inten-sity of the mutant forms is higher than that of the wild-type enzyme Moreover, with the L85A and L85A⁄ L276A mutants, the increase of fluorescence emission that corresponds to the dissociation of the cofactor is shifted towards lower urea concentrations with respect to wild-type and L276A forms (Fig 3) This observation is reminiscent of that noted for the internal aldimine and activity data, and indicates a shift of the equilibrium between the native and the intermediate forms in favour of the latter At urea con-centrations above 2.3 m, and as the protein unfolds completely, the fluorescence emission profiles of all enzyme forms coincide, suggesting that the equilibrium between the denaturation intermediate and the unfolded protein is not affected by the mutations The influence of the mutations on the far-UV CD and average lambda (for a definition, see Experimental procedures) profiles is not as clear as in the case of the activity and internal aldimine data (Fig 3E, F) The
CD signal and average lambda do not vary at a urea concentration in the range 0–1 m At a urea concentra-tion of 2.3 m, approximately one-third of the far-UV
CD signal is lost, although very little change of the average lambda is observed This indicates that the loss of cofactor that takes place in the first denatur-ation step does not correspond to large structural changes
Sedimentation velocity measurements
In a previous study [4], we reported that the L85A, L276A and L85A⁄ L276A mutations affect the quater-nary structure stability of eSHMT The wild-type enzyme is a dimer with molecular mass of approxi-mately 91 kDa and shows a single band in the sedimentation coefficient distribution with a maximum
Table 1 Parameters obtained from the global best-fit of activity
and internal aldimine data Parameters are expressed as the
mean ± SE determined by the global nonlinear least squares fitting
of data to Eqns (1,2), as detailed in the text K i represents the
cal-culated inhibition constant, whereas cm1and n reflect, respectively,
the urea concentration midpoints and the steepness of the
sigmoi-dal curves.
L85A ⁄ L276A 1.38 ± 0.06 1.56 ± 0.01 6.84 ± 0.35
Trang 5at 5.5 S (s20,w), which is the value expected for a
hydrated dimer with an approximately spherical shape
The hydrophobic cluster mutations shifted the
equilib-rium between dimeric and monomeric forms of the
enzyme in favour of the latter, which shows a
sedimen-tation coefficient of approximately 3 S Interestingly,
the monomeric form of the enzyme was shown to bind
PLP This observation is not unprecedented for Fold
Type I enzymes [10]
In the present study, ultracentrifugation experiments
were carried out aiming to analyse the effect of urea
on the sedimentation properties of wild-type and
mutant eSHMTs Sedimentation velocity experiments
were performed in the presence of either 1 or 2.3 m
urea These concentrations correspond to crucial
events in the denaturation mechanism: exposure of the
enzyme to 1 m urea results in the loss of half of the
catalytic activity, although all the cofactor is retained
at the active site as internal aldimine In 2.3 m urea,
the cofactor is lost as the denaturation intermediate is
formed (Fig 2) In Table 2, the results of the present
ultracentrifuge analysis are compared with those
obtained in the absence of urea [4] In 1 m urea, the
wild-type enzyme is dimeric, but becomes mainly
monomeric when the urea concentration is increased
up to 2.3 m, as indicated by a predominant band with
a maximum at 3.1 S in the sedimentation coefficient distribution (Fig 4) The frictional ratio (f⁄ f0) (i.e the ratio between the experimentally calculated friction coefficient and the minimum friction coefficient of an anhydrous sphere) of monomeric wild-type eSHMT is
Fig 3 Spectroscopic analysis of
urea-induced unfolding of wild-type (d), L85A (D),
L276A (h) and L85A ⁄ L276A ()) enzyme
forms All spectroscopic measurements
were carried out on enzyme samples at a
concentration of 2.3 l M , in 50 m M NaHepes
(pH 7.2), containing 200 l M dithiothreitol
and 100 l M EDTA at 20 C Intrinsic
fluores-cence emission measurements at 336 nm
on wild-type and mutant forms were
per-formed with a 1 cm quartz cuvette upon
excitation at 295 nm (A) Comparison
among relative fluorescence emission (Fr)
and retained fractions (f ) of activity (s)
and internal aldimine (·) measured with
wild-type eSHMT as a function of the urea
concentration (B–D) Relative fluorescence
denaturation profiles obtained with wild-type
and mutant enzymes (E) Molar ellipticity at
222 nm ([h]222) calculated from far-UV CD
measurements carried out in a 0.2 cm
quartz cuvette (F) Average lambda (k)
pro-files calculated from fluorescence emission
spectra acquired from 320–500 nm, with
excitation at 295 nm.
Table 2 Sedimentation coefficients calculated from ultracentrifuge experiments on wild-type and mutant eSHMTs The frictional ratio (f ⁄ f 0 ) is the ratio between the experimentally calculated friction coefficient and the minimum friction coefficient of an anhydrous sphere.
s20, w(S)
Wild-type 5.5 (f ⁄ f 0 = 1.2) 5.4 (f ⁄ f 0 = 1.2) 5.5 (17%)
3.1 (83%) L85A 5.5 (f ⁄ f 0 = 1.2) 5.3 (88%)
2.9 (12%)
6.4 (10%) 2.8 (90%) L276A 5.5 (f ⁄ f 0 = 1.2) 5.5 (77%)
3.1 (23%)
2.5 (f ⁄ f 0 = 1.5)
L85A ⁄ L276A 5.5 (66%)
3.3 (34%)
5.5 (35%) 3.3 (65%)
2.5 (f ⁄ f 0 = 1.5)
Trang 6equal to that of its dimeric form (1.2) and close to that
of a spherical protein, suggesting that the subunit
dissociation took place without any large structural
denaturation
With all mutant forms, 1 m urea determines the
partial dissociation of the dimer subunits (Fig 4 and
Table 2) The extent of dissociation is greater for the
double mutant, which already exists as an equilibrium
mixture of monomers and dimers in the absence of
urea, and is smaller for the L85A mutant and
interme-diate for the L276A mutant Nothing may be
con-cluded regarding the shape of the mutant monomeric
forms in 1 m urea because the frictional ratio cannot
be calculated when more than one sedimentation
species is present at equilibrium However, a
sedimen-tation coefficient of approximately 3 S suggests that all
monomers have an approximately spherical shape in
1 m urea It should be noted that, with all mutant
forms, the dissociation of subunits in 1 m urea takes
place without any loss of cofactor (Fig 2), in
agree-ment with a substantial retention of the active site
native structure By contrast, with the wild-type
enzyme, the dissociation of subunits is observed at a
much higher urea concentration range (1–2.3 m),
apparently in concomitance with the loss of cofactor
In 2.3 m urea, the L276A and L85A⁄ L276A mutant
forms exist as single sedimentation species with a
coef-ficient of 2.5 S The frictional ratio calculated for this
species is 1.5, suggesting that the decrease in the
sedi-mentation coefficient is determined by the loss of
spherical shape as a result of a partial structural dena-turation of the monomer The L85A mutant in 2.3 m urea is present as two sedimentation species with coef-ficients of 2.8 S and 6.4 S The 6.4 S species most probably results from aggregation The 2.8 S species, which shows a broad coefficient distribution, may also correspond to a partially denatured monomer
PLP-binding properties of the monomeric denaturation intermediate
The cofactor binding properties of monomeric wild-type and mutant enzymes in 2.3 m urea (dissolved in the same buffer used in the previous experiments) were analysed in order to probe the structural features of the active site The visible absorption spectrum of wild-type eSHMT shows a characteristic absorption band with maximum at 420 nm, as a result of the pres-ence of PLP bound at the active site as a protonated internal aldimine [11] The absorption spectra of the enzymes (10 lm subunit concentration) in 2.3 m urea were recorded and subtracted from the absorption spectra acquired after 20 min subsequent to the addi-tion of 100 lm PLP, allowing sufficient time for the cofactor binding equilibrium to be reached (as indi-cated by the fact that the absorption spectrum stopped changing) The differential spectrum obtained with the wild-type enzyme (Fig 5) clearly results from the development of a positive 420 nm absorbing band, demonstratring that the addition of PLP determines
Fig 4 Sedimentation velocity distributions obtained with wild-type and mutant eSHMTs Sedimentation velocity measure-ments were performed at 116 480 g on 2.5 l M (subunit concentration) enzyme sam-ples kept at 20 C in 50 m M NaHepes buffer (pH 7.2) in the absence (——) or presence
of 1 M (- - - -) and 2.3 M urea (ÆÆÆÆÆ).
Trang 7the formation of a native-like internal aldimine The
differential spectra recorded with the mutant enzymes
indicate the formation of a band with maximum
absorbance at lower wavelengths (at approximately
390–400 nm) Evidently, in 2.3 m urea, PLP binds to
the mutant enzymes, but without the formation of a
native-like internal aldimine, suggesting a structural
difference between the mutant active site and the
wild-type
Discussion
Previous studies [5,8,9] show that the urea-induced
denaturation of wild-type eSHMT, from a native
dimer to a fully denatured monomer, takes place
according to a three-state mechanism (Scheme 1A), in
which an intermediate catalytically inactive apo-form
of the enzyme mostly accumulates at a urea
concentra-tion of approximately 2.3 m The data obtained in the
present study show that, at this urea concentration,
the enzyme has lost most of the cofactor (Fig 2) and
is in a monomeric form (Fig 4 and Table 2) There-fore, the urea-induced loss of cofactor and dissociation
of subunits appear to be simultaneous events of the first denaturation step (N2PLP¢
þPLP2I in Scheme 1A) The dissociation of subunits apparently takes place without any large denaturation of the monomer structure This
is suggested by the fact that the enzyme monomers in 2.3 m urea retain a spherical shape, as indicated by the frictional ratio (f⁄ f0) and the sedimentation coefficient calculated from the ultracentrifuge analysis (Table 2) The minor change of the far-UV CD spectrum observed when the urea concentration is increased up
to 2.3 m is therefore hardly attributable to a loss of secondary structure, and may instead result from a conformational change of the protein monomer Upon PLP binding, the native apo-eSHMT is known to undergo a conformational change, which most proba-bly results from a shift of the equilibrium between the open and closed forms of the enzyme [12] Urea might act to shift this equilibrium in favour of the open form, promoting PLP dissociation from the active site The wild-type enzyme in 2.3 m urea, which is mostly monomeric and in the apo-form, maintains the capa-bility to form a native-like internal aldimine if a large excess of PLP is added (Fig 5) Increasing the urea concentration from 2.3 to 8 m determines the complete unfolding of the enzyme (2I¢2U in Scheme 1A), with
a complete loss of secondary structure, as reported in previous studies [5,8,9], and as can be deduced from the spectroscopic data shown in Fig 3 In this higher urea concentration range, the denaturation profiles obtained with the mutant enzymes do not differ from those of wild-type eSHMT
Mutations clearly influence the apparent denatur-ation mechanism of the enzyme at a urea concentra-tion in the range 0–2.3 m Comparison of data obtained from the ultracentrifuge analysis and from the measurement of covalently bound cofactor shows that, in contrast to that observed with the wild-type enzyme, with the mutant forms, the urea-induced sub-unit dissociation is detectable as a separate process with respect to the dissociation of PLP With all three mutant forms, at a urea concentration of 1 m, subunit dissociation is clearly visible (N2¢2N in Scheme 1B), whereas the loss of cofactor is negligible and becomes visible only at higher denaturant concentrations (2N ¢PLP
þPLP2I0; Scheme 1B) This observation agrees with the previously published data, indicating that the monomeric form of the enzyme is able to bind PLP and that the third cluster of CHCs plays an important role in the stabilization of the eSHMT quaternary structure [4] The extent of subunit dissociation in 1 m
Fig 5 Analysis of PLP-binding properties of wild-type and mutant
enzymes in 2.3 M urea Separate enzyme (20 l M ) and PLP (200 l M )
samples were kept in 2.3 M urea at 20 C for 15 h Equal volumes
of enzyme and PLP samples were then mixed and absorption
spec-tra recorded after 20 min Absorption specspec-tra of enzyme samples
mixed with an equal volume of buffer containing 2.3 M urea were
subtracted from spectra acquired in the presence of PLP,
generat-ing the differential spectra shown: wild-type eSHMT (——), L85A
(- - - -), L276A (ÆÆÆÆÆ) and L85A ⁄ L276A (ÆÆ-ÆÆ) mutants.
A
B
Scheme 1 Presumed equilibrium denaturation mechanisms of
wild-type (A) and mutant (B) eSHMTs N and U represent,
respec-tively, the native and the fully denatured forms of the enzyme
subunits The denaturation intermediate formed by the wild-type
enzyme is indicated by I, whereas I¢ represents the partially
dena-tured intermediate formed by the mutant enzymes.
Trang 8urea is higher for the double L85A⁄ L276A form, lower
for the L85A form and intermediate for the L276A
mutant This situation again reflects what is observed
for the same enzyme forms under native conditions [4]
A novel observation is that the mutations clearly
affected the process of PLP dissociation induced by
urea The L85A and L85A⁄ L276A mutations lowered
the midpoint of this transition and the L276A
muta-tion lowered its cooperativity (Table 1) Moreover,
upon PLP dissociation in 2.3 m urea, the monomeric
mutant enzymes appear to be partially denatured (I¢ in
Scheme 1B), as indicated by the frictional ratio and
the sedimentation coefficients calculated from the
ultracentrifuge analysis (Table 2) The extent of
dena-turation of this monomeric intermediate is not
expected to be very large because the average lambda
profiles of the wild-type and mutant enzymes are very
similar (Fig 3) Nevertheless, the addition of excess
PLP to the partially denaturated monomer does not
result in the formation of a native internal aldimine
Evidently, the concentration of the species at
equilib-rium cannot be altered by the addition of PLP,
con-firming that the mutant enzymes follow a different
denaturation mechanism with respect to wild-type
eSHMT Taken together, these observations suggest
that, in the mutant enzymes, the urea-induced
dissocia-tion of PLP is favoured by the disrupdissocia-tion of the third
cluster of CHCs The mutations introduced with the
aim of reducing the hydrophobic surface contacts have
instead reduced the stability of the PLP binding site
This conclusion points to a clear relationship between
the formation of the cluster and the structural integrity
of the active site
By contrast to the CHCs located in the cores of the
large and small domains, the cluster under study is not
directly involved in the positioning or stability of any
active site or PLP-binding residue Considering the
studies on eSHMT folding, we suggest that this cluster
may play a fundamental role in the folding mechanism
of the enzyme, which may be divided into two phases
[5,8,9,13] In the first phase, the large and small
domains rapidly assume their native state, forming a
folding intermediate that has almost all of the native
secondary and tertiary structure, but is unable to bind
PLP In this intermediate, the N-terminus and an
inter-domain segment remain exposed to solvent [8]
(Fig 1B) In the second, slower phase, these structural
elements fold into the native structure, conferring the
enzyme with the capability of binding PLP Because
the interdomain segment comprises the a-helix
contrib-uting L276 and the second a-helix (where L85 is
located) of the cluster is part of the large domain, it
follows that the last folding event may correspond to
the formation of the third cluster of CHCs The for-mation of the cluster presumably fastens together all the structural components of the protein and confers stability to the active site The high degree of sequence and structural conservation of the third cluster of CHCs, as observed for the majority of fold-type I enzymes, suggests that this function, which is hypothe-sized for eSHMT, could be extended to the whole superfamily
Experimental procedures
Materials
Ingredients for bacterial growth were obtained from Sigma-Aldrich (St Louis, MO, USA) Chemicals for the purification of the enzymes were obtained from BDH (Poole, UK); DEAE-sepharose and phenyl-sepharose were obtained from GE Healthcare (Milwaukee, WI, USA) The
E coli glyA (SHMT encoding gene) were already available from a previous study [4] Wild-type and mutant forms of eSHMT were purified as described previously [14] PLP was added to protein samples during the purification procedure, but it was left out in the final dialysis step All experiments
7.2, containing 200 lm dithiothreitol and 100 lm EDTA PLP was obtained from Sigma-Aldrich (98% pure) All other reagents were obtained from Sigma-Aldrich
Preparation of holoenzyme samples
We noted that different batches of purified eSHMT samples
observation was made with either wild-type or mutant forms of the enzyme To carry out comparable experiments,
it was mandatory to prepare enzyme samples that con-tained the same fraction of protein-bound PLP (possibly close to saturation) and, at the same time, were devoid of any excess of cofactor Holoenzymes were then prepared from apoenzyme samples, by the addition of PLP at the concentration needed to obtain 98% saturation, as calcu-lated on the basis of the recalcu-lated dissociation constant of PLP binding equilibrium [4] The subunit concentration of the holoenzyme was calculated according to a molar absorptivity value of e280= 44884 cm)1Æm)1 [12] Apoen-zyme samples were prepared as described previously [5]
Unfolding and refolding experiments
Concentrated protein samples were diluted into urea solu-tions (0–7.9 m in 50 mm NaHepes, pH 7.2, containing
obtain a final protein concentration of 2.3 lm
Trang 9Spectro-scopic measurements, activity assays, measurements of
internal aldimine and ultracentrifuge analyses were carried
out after 15 h, which allows sufficient time to reach the
equilibrium [5]
The l-threo-3-phenylserine cleavage activity of
urea-incubated enzyme samples was measured after the direct
addition of 7.5 mm substrate, which corresponds to
approx-imately 16% saturation The dilution of urea resulting from
substrate addition was taken into account
The reversibility of the urea-induced unfolding was
ana-lyzed by means of refolding experiments in which denatured
enzyme samples (23 lm kept with 8 m urea in 50 mm
NaHepes, pH 7.2, containing 200 lm dithiothreitol and
100 lm EDTA for 15 h at 20C) were diluted ten-fold with
buffer at 20C These conditions have been shown to give
the highest yield of refolded enzyme [5] Four hours later,
after allowing sufficient time to complete the refolding
pro-cess [5], the enzyme activity of the refolded sample was
assayed upon a further 50-fold dilution of the sample into
the assay reaction mixture (the final enzyme concentration
in the activity assay was 0.05 lm) Ten-fold molar excess
PLP was added to refolded samples immediately before
dilution into the activity assay reaction mixture
Activity assays
(pH 7.2), containing 200 lm dithiothreitol and 100 lm
EDTA The rate of l-threo-3-phenylserine cleavage (3 lm
enzyme samples) was obtained from spectroscopic
measure-ment of benzaldehyde production at 279 nm, employing a
molar absorptivity value of e279= 1400 cm)1Æm)1[15,16]
Spectroscopic measurements
Fluorescence emission measurements were carried out with
a LS50B spectrofluorimeter (Perkin Elmer Life Sciences,
Waltham, MA, USA) using a 1 cm path length quartz
cuvette Fluorescence emission spectra were recorded in the
range 320–500 nm (1 nm sampling interval; 5 nm emission
slit), with the excitation wavelength set at 295 nm (3 nm
excitation slit) Fluorescence measurements were expressed
as relative fluorescence intensity and average lambda
(aver-age lambda = R(Ii· ki)⁄ R(Ii), where ki is the ith
wave-length and Ii is the corresponding relative fluorescence
intensity)
Far-UV (190–250 nm) CD spectra were measured using a
0.2 cm path length quartz cuvette and expressed as the mean
residue ellipticity [Q], assuming a mean residue molecular
mass of 110 per amino acid residue UV-visible spectra were
recorded with a double-beam Lambda 16 spectrophotometer
(Perkin Elmer Life Sciences) Kinetic measurements in the
activity assays were performed on a Hewlett-Packard 8453
diode-array spectrophotometer (Hewlett-Packard, Palo Alto,
CA, USA) All spectroscopic measurements were carried out
dithiothreitol and 100 lm EDTA
Analytical ultracentrifugation analysis
Sedimentation velocity experiments were carried out at
dithiothreitol and 100 lm EDTA, on a Beckman XL-I ana-lytical ultracentrifuge (Beckman Coulter, Fullerton, CA, USA) equipped with absorbance optics and an An60-Ti rotor In the sedimentation velocity experiments, performed
at 116 480 g, the protein concentration was 2.5 lm Data were collected at 277 nm at a spacing of 0.003 cm with three averages being obtained in a continuous scan mode Sedimentation coefficients and integration of data were obtained using the software sedfit (provided by P Schuck, National Institutes of Health, Bethesda, MD, USA) The values were reduced to water (S20,w) using standard proce-dures The buffer density and viscosity were calculated using the software sednterp (http://www.jphilo.mailway com) The ratio f⁄ f0was calculated from the diffusion coef-ficient, which in turn is related to the spreading of the boundary, using the software sedfit
Internal aldimine measurements
Borohydride (BH4)) is known to reduce imines and alde-hydes rapidly and efficiently [17] When the internal aldi-mine (PLP-enzyme Schiff base) of PLP-dependent enzymes
is reduced with BH4 ), the cofactor is irreversibly attached
to the protein, giving an absorption spectrum with a band
concentrated solution (5 m) in 50 mm NaOH and added to proteins samples (2.3 lm in 8 mL of 50 mm NaHepes buf-fer at pH 7.2, containing 200 lm dithiothreitol and 100 lm EDTA) incubated with urea, so that its final concentration was 83 mm Thirty minutes after the addition of NaBH4, protein samples were concentrated in Amicon Ultra centri-fuge filters (30 kDa cut-off; Millipore, Billerica, MA, USA) and diluted with 50 mm NaHepes buffer repeatedly in order
to eliminate low-molecular mass molecules, including the reduced free cofactor In the final dilution step, the buffer was added to obtain a final volume of 2 mL and absorption spectra were recorded The A335⁄ A280 ratio was calculated
to normalize the absorbance of the reduced internal aldi-mine on the basis of protein concentration, and then divided by the ratio found for a native, PLP-saturate enzyme sample The result obtained gave the fraction of PLP molecules bound per monomer of enzyme
Data analysis
The equilibrium unfolding profiles obtained from the mea-surement of the internal aldimine and the catalytic activity
Trang 10were expressed as fraction of the related measurements
car-ried out in the absence of urea and analyzed, respectively,
according to Eqns (1,2) Equation (1) describes a sigmoid
curve and conforms to a two-state denaturation process
Equation (2) takes into account both the inhibitory and
denaturing effects of urea on the catalytic activity of the
enzyme The enzyme in the presence of urea is assumed to
exist as a mixture of free, active enzyme and urea-bound
inactive enzyme at equilibrium Both enzyme forms are also
assumed to denature according to an identical sigmoid
pro-cess (Eqn 1) In the equations, f represents the fraction of
either internal aldimine (Eqn 1) or activity (Eqn 2), n
reflects the steepness of the sigmoid transition, and cmis its
urea concentration midpoint In Eqn (2), Ki is the
inhibi-tion constant of the urea binding equilibrium
f¼ 1 ½urea
n
c n
f ¼ 1 ½urea
n
c n
m þ urea½ n
1 ½urea
urea
½ þ Ki
ð2Þ
Internal aldimine and activity data were fitted in a global
least squares minimization procedure in which the
parame-ters of the sigmoid denaturation processes contained in
Eqns (1,2) were shared, using the software prism
(Graph-Pad Software Inc., La Jolla, CA, USA)
Acknowledgements
We thank Professor Verne Schirch for helpful
discus-sions This work was supported by grants from the
Italian Ministero dell’Universita` e della Ricerca Rita
Florio is the recipient of a fellowship from the Facolta`
di Scienze Matematiche, Fisiche e Naturali of
‘Sapien-za’ Universita` di Roma, Italy
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