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First published online November 30, 2007
Journal of Experimental Biology 210, 4307-4318 (2007)
Published by The Company of Biologists 2007
doi: 10.1242/jeb.009753
Holdfast heroics: comparing the molecular and mechanical properties of Mytilus californianus byssal threads
Department of Molecular, Cellular, and Developmental Biology, University of California at Santa Barbara (UCSB), Santa Barbara, CA 93106, USA
* Author for correspondence (e-mail: harringt{at}lifesci.ucsb.edu)
Accepted 2 October 2007
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Summary |
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The preCols from M. californianus are more divergent from the other two species than they are from one another. However, the degree of divergence is not uniform among the various domains of the preCols, allowing us to speculate on their mechanical role. For instance, the extra spider silk-like runs of alanine-rich sequence in the flanking domains of M. californianus may increase crystalline order, enhancing strength and stiffness. Histidine-rich domains at the termini, in contrast, are highly conserved between species, suggesting a mechanical role common to all three. Mechanical testing of pH-treated and chemically derivatized distal threads strongly suggests that histidine side chains are ligands in reversible, metal-mediated cross-links in situ. By combining the mechanical and sequence data, yield and self-healing in the distal region of threads have been modeled to emphasize the intricate interplay of enthalpic and entropic effects during tensile load and recovery.
Key words: mussel, byssus, self-healing, histidine–metal, collagen
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Introduction |
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TOPSummaryIntroductionMaterials and methodsResultsDiscussionReferences |
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). In addition,
the byssus is emerging as an important paradigm for the bio-inspired
engineering of water-resistant adhesives
(Lee et al., 2006),
functionally graded polymers (van Hest and
Tirrell, 2001; Waite et al.,
2004), and injection molding of liquid crystals
(Hassenkam et al., 2004). The
utility of such paradigms relies on the depth to which
structure–function relationships are understood. A particularly
effective strategy for defining structure–function relationships is to
investigate homologous structures in closely related species
(Hayashi et al., 1999;
Brooks et al., 2005). With this
report, byssal thread mechanics and the protein chemistry of three species of
Mytilus are compared. Of these, the byssus of the California mussel
Mytilus californianus (Conrad), stands out as mechanically
superior.
The threads that make up the byssus of M. californianus are
several centimeters long with a diameter of about 200 µm, function outside
the body of the organism, and are formed from soluble protein precursors
secreted by the foot of the mussel. Byssal threads are subdivided into four
morphologically and mechanically distinct regions: the stem, the plaque, and
the proximal and the distal portions of the thread
(Fig. 1). The stem attaches the
thread to the mussel tissue, and the plaque contains the adhesive that
connects the thread to the hard substratum. The thread connecting the stem to
the plaque is further divided into two mechanically distinct regions. The
proximal end (closest to the organism) is extensible up to 200% of its
original length, has a low initial stiffness, and a corrugated appearance. The
distal portion of the thread, in contrast, is characterized by a high initial
stiffness followed by a yield point at about 15% strain and a noticeable
stress softening (Bell and Gosline,
1996). For most engineered polymeric materials, yield is not
reversible and leads to permanent deformation rendering the material
functionally useless. However, in distal threads, damage due to yield is
reversible in a time-dependent, self-healing manner with threads recovering
25% of the lost modulus and strain energy in 10 min following a cycle to 35%
strain (Carrington and Gosline,
2004).
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). Once committed, soluble thread precursors are secreted into
the ventral groove of the foot where muscular contractions mold them into
functional threads. The whole process takes a total of 2–5 min. The main
protein component preCol, also known as byssal collagen, makes up 96% of
distal thread and 66% of the proximal
(Waite et al., 2002). There
are three preCol variants, each of which is divided into several distinct
domains with particular motifs resembling known structural proteins.
Each preCol has a central collagen domain, which deviates from fibrillar
collagens (Types I, II, III, V and XI) in containing 1–5 interruptions
in the canonically repeated Gly-X-Y collagen sequence. These substitutions and
deletions are believed to cause bends in the normal rod-like shape of the
collagen trimer as exhibited in the C1q heterotrimer
(Kilchherr et al., 1985), and
several other invertebrate collagens
(Sicot et al., 1997;
Fowler et al., 2000). It has
been experimentally demonstrated that proline or hydroxyproline in the X and Y
position produce the most stable triple helix and all other amino acid
residues have a tendency to destabilize the helix
(Persikov et al., 2005). In
the preCol collagen domain the X and Y residues tend to be destabilizing
residues. Despite this and the breaks in the repeat structure, the presence of
a stable collagen triple helix is suggested in threads by wide angle X-ray
scattering of distal threads (Mercer,
1952; Rudall,
1955) as well as by the resistance of the byssal collagens to
pepsin treatment (Qin and Waite,
1995).
At either end of the collagen region are flanking domains that differ
between the three variants and resemble motifs of known load-bearing proteins.
PreCol D, which is dominant in the distal end of the thread and decreases in
abundance axially toward the proximal end
(Fig. 1), has flanking domains
that resemble a motif sequence of spider dragline silk. PreCol P, which exists
in a gradient complementary to preCol D, has flanking regions that closely
resemble elastin, and preCol NG, which is uniformly present throughout the
thread, has Gly-rich flanking domains that resemble plant cell wall proteins
(Waite et al., 1998). Since
the mechanical properties of dragline silk (as in preCol D) differ
substantially from elastin (as in preCol P), the graded distribution of
preCols with different flanking regions is suspected to play a major role in
the graded mechanical properties along the distal to proximal axis
(Waite et al., 2002).
Beyond the flanks, at the N- and C-termini are regions with abundant
histidine and 2–4 residues of dihydroxyphenylalanine (DOPA), which is a
post-translational modification of tyrosine common to other byssal proteins in
the plaque and outer coating of the thread. The histidines are proposed to be
reversible ligands for coordination bonds with transition metal ions such as
zinc(II) and copper(II), as demonstrated with shorter synthetic peptides
(Waite et al., 1998;
Schmitt et al., 2000). Such
reversibly broken coordination complexes are stronger than non-covalent bonds,
but possess only half the strength of a covalent bond
(Lee et al., 2006) and are
suspected to play an integral role as sacrificial bonds in yield and
self-healing in the distal portion of the thread. DiDOPA cross-links have been
proposed as covalent bonds linking preCols end to end
(Waite et al., 2002).
Many species of mussels produce a byssus, but the component threads of
byssi from different species are not mechanically equivalent
(Brazee and Carrington, 2006).
There are five species in the genus Mytilus including M.
galloprovinicialis Lamarck, M. edulis Linnaeus, and M.
californianus Conrad (Gosling,
1992). M. californianus is phylogenetically distant from
M. galloprovincialis and M. edulis and is readily
distinguishable from them (Santaclara et
al., 2006). Whereas the mechanical properties of the threads of
M. galloprovinicialis and M. edulis are very similar to one
another (Lucas et al., 2002),
M. californianus has much thicker and mechanically superior threads.
M. californianus distal threads are 2–3 times stiffer and 30%
more extensible than distal threads from the other two species
(Bell and Gosline, 1996).
Distal threads from M. californianus also self-heal more quickly than
those of M. edulis and M. galloprovincialis after yield
(Carrington and Gosline, 2004).
These mechanical differences are probably related to adaptations in M.
californianus that help it survive in the more exposed, wave-swept parts
of the intertidal. Interestingly, these differences appear limited to the
distal region since mechanical testing of the proximal region has not revealed
significant differences in modulus, strength or extensibility between the
three species (Bell and Gosline,
1996).
cDNA sequence has been deduced for all three preCols from M.
galloprovinicialis and M. edulis
(Qin et al., 1997;
Coyne et al., 1997;
Qin and Waite, 1998;
Lucas et al., 2002), but not
for M. californianus. The purpose of this study was twofold: (i) to
determine the complete primary sequence of collagenous preCols from M.
californianus to enable a direct comparison with those from other
species, and (ii) to reconcile both divergent and conserved features of preCol
biochemistry with the comparative mechanical performance of the distal portion
of the byssal thread. The results suggest that the single most influential
factor in the tensile superiority of M. californianus is the greater
abundance of silk-like polyalanine tracts and that the highly conserved
histidine-rich domains play an integral role as sacrificial bonds in threads
of all three species.
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Materials and methods |
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PCR amplification and cloning of the preCols
Primers designed for the preCols from Mytilus edulis
(Lucas et al., 2002) and
degenerate primers based on highly conserved sequence in M. edulis
and M. galloprovincialis were used to screen the M.
californianus cDNA, assuming some sequence similarity. Preliminary
sequence obtained with these primers was used to create gene-specific primers
used in PCR, 5' RACE and 3' RACE to obtain the remaining sequence.
Regions of sequence where degenerate primers or primers for M. edulis
landed were confirmed by overlap with sequence-specific primers. The universal
primer mix supplied with the RACE kit (Clontech) was used for 5' and
3' RACE. The relevant reactions are described in
Table 1.
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PCR and RACE products were cloned into Pgem-T Easy plasmid (Promega,
Madison, WI, USA) and transformed into One Shot chemically competent E.
coli cells (Invitrogen, Carlsbad, CA, USA). Miniprepped plasmids were
contractually sequenced (UC Davis DNA Sequencing Facility) and overlapping
sequences were assembled and translated to give the deduced protein sequences.
M. californianus preCol cDNA sequences were entered into GenBank
under accession numbers EU120661, EU120662 and EU120663 for preCol D, NG and
P, respectively. The deduced protein sequences from the cDNA were compared to
preCol sequence from M. galloprovincialis and M. edulis in
the database using ClustalW on the EBI server
(Chenna et al., 2003) to
determine percent identity between specific preCol variants of the three
species. Alignments were performed with the identity matrix using default
settings for all the other parameters.
Mechanical testing
Distal portions of fresh tank-grown threads were dissected from M.
californianus and allowed to rest in seawater for at least 48 h prior to
testing. Thread ends were secured between pieces of cardstock with
cyanoacrylate glue. The thread cross-section was assumed to be slightly
elliptical, and the area was calculated using the average of the long and
short side as the diameter. Cardstock loaded threads were placed in the grips
of a Bionix 200 tensile tester (MTS, Eden Prairie, MN, USA) and subjected to
mechanical testing. Threads were hydrated by submersion in seawater or buffer
immediately prior to tensile testing, which was performed within an MTS
environmental chamber with the relative humidity raised to 99.9±5% in
order to maintain thread hydration. Testing at high humidity was necessary to
reduce slippage of the thread from the cardstock at higher strains, which was
seen in test runs with submerged threads. Threads were cycled consecutively to
10, 20, 30, 40, 50, 60% strain, and finally to break, at an extension rate of
5 mm min–1 with no rest between, recording the extension and
load on MTS Testworks 4 software. Extension was converted to engineering
strain using the equation
=(l–lo)/lo where
l is the extension of the thread during tensile loading and
lo is initial length of the unloaded thread with zero
load. Load data were converted to engineering stress using the equation
=F/A, where F is the tensile force applied
to the thread and A is the cross-sectional area of the thread.
Young's modulus (E, stiffness) for each strain interval was
determined as the maximum slope of the stress–strain curve during
loading after the characteristic toe region. To assess the stress softening
incurred with each successive yield, the modulus of each cycle is presented as
a percentage loss of the initial stiffness (%
loss=[1–E/Eo]x100%) where E
is the stiffness of a particular cycle and Eo is the
stiffness measured during the first cycle of a previously unstrained
thread.
Histidine–metal coordination cross-links are suspected to play an
important role in yield and hysteresis in the distal threads. Such bonds,
however, are known to be pH sensitive since they depend on the deprotonation
of a histidine nitrogen, with a pKa 
6.5
(Fig. 2). In order to
investigate the effect of pH on mechanical performance and, by extension, on
histidine–metal cross-links, threads were treated in citrate-phosphate
buffer at pH 3, 4, 5, 6, 7 and 8 at 4°C for at least 24 h prior to
testing. A subset of threads was equilibrated in citrate-phosphate buffer at
pH 5.5 for 24 h and treated with diethylpyrocarbonate (DEPC) by adding an
tenfold molar excess (65 µmol l–1) to the buffered
solution (molar excess is based upon estimated concentration of His in a
thread). In moderate excess, DEPC reacts with histidine residues by
carbethoxylating one of the nitrogen atoms in the imidazole ring, rendering it
unable to participate in metal coordination complexes
(Fig. 2). The reaction was
performed at pH 5.5 since DEPC targeting of histidine residues
vis-à-vis other amino acids is highly specific there
(Lundblad, 2005). Although
metal-bound histidine is protected from attack by DEPC, at pH 5.5 there will
be some unbound, exposed histidine residues. DEPC-treated threads and a
control group of untreated threads at pH 5.5 were then re-equilibrated 24 h in
pH 8 buffer prior to mechanical testing. One-way analysis of variance (ANOVA)
was performed to compare differences in Young's modulus between treated
threads (pH and DEPC) and untreated threads (SW ctrl) during their first
strain cycle. A two-way ANOVA was performed to assess the effects of pH and
strain on the Young's modulus (E) of threads during multiple cycles
of increasing strain.
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Results |
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In M. californianus, the preCol variants are all slightly larger proteins than their counterparts in M. galloprovinicialis and M. edulis. Over the length of the whole protein, each particular variant from M. edulis is around 90% identical to the same variant in M. galloprovinicialis, whereas M. californianus variants are only 80% identical to their counterparts (Table 2). It should be noted that the alignment scores indicated in Table 2 represent the number of identities in the best match as determined by ClustalW divided by the number of residues aligned, and therefore do not account for inserts. Domains where the score does not accurately reflect the degree of divergence between species due to inserted sequence include the flanking and His-rich domains. This will be discussed later. All three collagen domains conserve the tendency for destabilizing residues in the X and Y positions of the canonical collagen repeat.
PreCol D
Table 2 reveals that the
collagen domain of preCol D is more conserved than the silk or His-rich
regions. However, there is one significant difference in the collagen that
will be potentially important to the function and assembly of the protein. As
mentioned, the preCol collagen regions are distinct from typical fibrillar
collagens in containing one to several deviations from the Gly-X-Y repeat
motif, which typically lead to kinks in the characteristically rod-like
collagen morphology (Kilchherr et al.,
1985). In preCol D of M. californianus there are three
aberrations in the collagen domain instead of the five seen in both M.
galloprovinicialis and M. edulis
(Fig. 3). Two of the
aberrations are typical deletions of a single Gly also seen in M.
galloprovinicialis and M. edulis, but they surround a novel
aberration not seen in the other two species in which the sequence
Val-Val-Gly-Gly is inserted between Gly-X-Y repeats. This is the first
instance of a four amino acid insert in a preCol collagen domain, but it is
uncertain how the triple helix would be perturbed by such an insert.
The alignment scores of both the N- and C-terminal silk domains are low compared to the collagen domain (67% and 69% identity, respectively, vs 93% when compared with M. edulis), but still do not fully represent the degree of deviation since both are significantly longer in M. californianus due to inserts. The inserts come in the form of two alanine-rich regions of 24 and 10 amino acid residues, respectively, in the N terminus (Fig. 6A) and three inserts of different sizes in the C terminus. If the number of identical residues in the N-terminal silk domain of M. edulis and M. californianus is divided by the number of residues in the larger of the two (M. californianus=95, M. edulis=55, M. galloprovincialis=55) instead of the number of aligned residues, the percent identity drops from 70% to about 40%, indicating the large amount of deviation in the flanking domains of M. californianus not accounted for by the ClustalW alignment score.
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The His-rich domains have a relatively low alignment score, but Fig. 6B reveals that while the sequence outside of the suspected metal binding motif is very divergent, the histidine containing sequence is highly conserved. Every single histidine in the N-terminal His-rich domain is conserved, along with Gly and Ala spacer residues. The C-terminal His-rich region is less conserved, but the number of His residues is mostly conserved with M. galloprovincialis having one extra histidine.
PreCol NG
Conservation of preCol NG domains in M. californianus
vis-à-vis preCol NG from the other two species parallels the
trends seen with preCol D. The collagen region shows the highest identity
score outside of the acidic patch and the signal sequence
(Table 2). The only aberration
is a single deletion of a glycine in the eleventh repeat
(Fig. 4), identical to that of
M. edulis. M. galloprovincialis has two additional deviations in the
form of substitutions of Gly with an Asp and an Arg, respectively.
The suspected His-rich metal binding motifs are less conserved in NG than in D, but are still relatively similar. The N-terminal His region of all three species has five histidine residues; however, in M. californianus the histidines are more closely packed. The C-terminal His-rich region is more conserved than the N-terminal, with 14 out of 17 histidine residues identical between all three species.
As with preCol D, the major differences are in the flanking domains (Table 2), especially the Gly-rich region within the C-terminal flanking domains, which contains numerous inserted regions rich in Gly, Val and Leu. Gly residues are mostly conserved between species, and the non-Gly residues exhibit variation but are always hydrophobic residues such as Ala, Leu and Val. The introduction of considerably more Pro in the flanking domains of NG in M. californianus than in the other two species is notable since it could lead to a more amorphous secondary structure.
PreCol P
Of the three variants, preCol P has the least conserved collagen domain at
83% identity with M. edulis (Table
2). However, the single Gly deletion in the eleventh Gly-X-Y
repeat (Fig. 5) is conserved in
all three species. The N-terminal His-rich domain of P is also the most
altered of the three variants in terms of the position and number of His
residues, but is still mostly conserved.
The flanking domains of preCol-P are again the least conserved regions with the C-terminal end having a 20% lower identity than the N-terminal. They are not as insertionally modified as the flanking domains of D and NG, but are more substituted. The C-terminal region is especially different and reminiscent of the flanking domains of preCol-NG in certain regions, with runs rich in Gly and Leu and many PGG repeats. A BLAST of the C-terminal flank sequence against the database shows it is over 50% similar to flagelliform spider silk whereas it is only about 60% similar to the C-terminal flanks of M. edulis and M. galloprovincialis.
Mechanical testing
Cyclic quasistatic mechanical testing
(Carrington and Gosline, 2004)
showed that the larger the strain that distal threads are pulled to, the
larger the resulting hysteresis. This study also revealed that the stiffness
disparity (stress softening) between the first and second cycles increased
with increasing strain of the first cycle. Both observations imply that damage
is occurring at the molecular level during yield and is intimately correlated
with hysteresis and reduction of modulus. The mechanical tests performed in
this study were designed to probe these observations more thoroughly and to
investigate more specifically the role of histidine–metal coordination
complexes as important sacrificial cross-links in tensile stress.
As Fig. 7A indicates, a distal thread incubated in seawater cycled to any strain within the yield region will have a second yield point if it is taken to a strain slightly beyond the maximum strain it achieved in the previous cycle. After each successive yield, threads show a reduction in modulus from that of the previous cycle. If the softening is presented as a percentage loss of the initial stiffness (% loss=[1–E/Eo]x100%) and plotted against the strain value that caused the reduction in stiffness (Fig. 7B), a few things become apparent. First, there is little softening observed during the 10% strain cycle, which is before the yield point typically occurs. The largest reduction in the stiffness occurs during the 20% strain cycle with the initial modulus reduced by almost 40% from the first cycle. Smaller reductions are seen after the 30% and 40% strain cycles, after which there does not appear to be further significant loss in modulus.
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). The stiffness vs pH curve follows the same trend
as the histidine titration curve that is plotted alongside it in light gray in
Fig. 8.
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The initial stiffness of threads incubated at pH 5.5 for 24 h and then re-equilibrated at pH 8 for 24 h are statistically indistinguishable from citrate-phosphate pH 8 and seawater threads (P<0.02), which demonstrates that the pH-induced reduction of stiffness is reversible (Fig. 8). Threads incubated at pH 5.5 in the presence of DEPC, and reequilibrated in citrate-phosphate buffer at pH 8 do not show this same reversibility and have a significantly different initial modulus from the control threads that went from pH 5.5 to pH 8 without DEPC treatment (P<0.02). As Fig. 8 shows, the initial modulus of DEPC-treated threads falls around 680 MN m–2, which is slightly below the mean value for threads treated in buffer at pH 7.
Plotting the modulus of each strain cycle against the preceding strain
value for each pH treatment (Fig.
9A) reveals that the pH-dependent stiffness variation seen in
Fig. 7 becomes less prominent
with increasing strain (two-way ANOVA, P<0.001). However, the
stiffness values of pH 8 and pH 5 treated threads are still significantly
different at all strains tested (P<0.01).
Fig. 9B shows the magnitude of
the modulus reduction (
E) caused by a particular strain cycle
plotted against the strain that caused it, revealing that for all pH
treatments the majority of damage occurs between 20–30% strain
(consistent with Fig. 7B).
Statistical analysis of E values at pH 5 and pH 8 reveals that
softening due to cycles of 20, 30 and 40% strain are significantly different
(P<0.01) whereas values at 10, 50 and 60% are not. It should be
noted that treatment at pH 5 and below does not eliminate stress softening
entirely, but it does greatly reduce the magnitude.
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The collagen domain, signal peptide and acidic patch are the most highly conserved regions between all three species with sequence identity between 83–100%. The His-rich domains have relatively low identity scores (77.3±11.3%), but closer examination of the whole domain reveals that the putative metal binding motifs are very well preserved. For all three variants the largest sequence deviations are localized in the flanking domains (mean identity score=70.0±8.5%), which are highly substituted in M. californianus. In every case except for the N-terminal flank in preCol P, M. californianus flanking domains are also significantly longer due to multiple insert regions.
Flanking domains
As stated earlier, the gradient of the variants is believed to be
responsible for the graded stiffness from distal to proximal, and the flanking
domains are believed to play a major role in these mechanical differences
because of their similarity to known structural proteins of varying stiffness
(Waite et al., 2002). Thus,
significant changes in the sequence of these domains in a particular variant
between species should affect the stiffness of the threads. Spiders use a
similar strategy to create a toolkit of silks with a range of mechanical
properties by adjusting the presence and amount of certain modules associated
with stiffness or elasticity. For example, polyalanine runs are associated
with beta sheet formation and stiffening of the silk, whereas GPGXX sequences
are thought to confer elasticity (Hayashi
and Lewis, 1998). In this light, the extra polyalanine runs in the
silk-like flanking domains of preCol D of M. californianus could
stiffen the molecule by adding more beta sheet crystal structure, which could
in turn stiffen the whole distal portion of the thread. Evidence for
beta-sheet structure in byssal threads has been seen in wide angle X-rays of
the distal region (Mercer,
1952; Rudall,
1955). In contrast, the increased proline content of the NG
flanking domains could reduce the amount of secondary structure and add more
entropic elasticity to the region.
PreCol P also shows significant changes in the C-terminal flanking domain
including Gly- and Leu-rich runs reminiscent of preCol NG and a
[GGP]12 repeat motif not present in the other two species. A BLAST
of the sequence reveals it has over 50% similarity to flagelliform silk rather
than elastin as in M. galloprovincialis and M. edulis.
Although the flanking domains of preCol P in M. californianus are
significantly different from those of the congeners, previous studies have
shown that the mechanical properties of the proximal region do not vary
between the three species (Bell and
Gosline, 1996). It is worth recalling that preCols make up only
66% of the proximal region (Waite et al.,
2002). Consequently, contributions of proteins such as ptmp-1
(Sun et al., 2002) in the
remaining 34% could significantly obscure detection of the mechanical effect
of subtle variations in preCol P.
Collagen domain
The collagen domains of the three variants are highly conserved between all
three species, maintaining both the presence of destabilizing residues and
aberrations in the Gly-X-Y repeat sequence. Fibrillar collagens (types I, II,
III, V and XI) show no tolerance for breaks in the Gly-X-Y repeat structure;
however, breaks regularly occur in non-fibrillar collagen (types IV and VIII)
(Soininen et al., 1987;
Brazel et al., 1987;
Yamaguchi et al., 1989).
Although deviations are commonplace in these non-fibrillar collagens,
deleterious Gly missense mutations do occur in type IV collagen
(Hudson et al., 2003),
suggesting that non-lethal breaks in the collagen repeat sequence are
site-specific and serve a functional purpose.
Model peptides based on the Gly-X-Gly deletions of Type VIII collagen have
been shown by X-ray crystallography to align into layers with the deleted
regions lined up (Bella et al.,
2006). This is very reminiscent of the smectic ordering of preCols
seen in byssal threads by atomic force microscopy (AFM)
(Hassenkam et al., 2004).
Bella et al. suggest the deletion may provide a `registration marker' favoring
in-register parallel packing rather than the quarter stagger typical of
fibrillar collagens (Bella et al.,
2006). It is possible that the highly conserved breaks in the
Gly-X-Y sequence of the preCols are similarly directing the smectic packing in
byssal threads, which has been proposed to have important mechanical
consequences for the thread as a whole.
(Gly-Pro-Hyp)n is the sequence paradigm for producing a
thermally stable triple helix, and deviations in the form of less stabilizing
residues in the X or Y position or breaks in the triplet will lead to a less
stable conformation (Persikov et al.,
2005; Bella et al.,
2006). PreCols are wrought with breaks and aberrations from this
stable paradigm that should obviate helix formation, yet they still form
triple helices and, at low strains, exhibit mechanical properties appropriate
for collagens. It is interesting that the mussel would have such an unstable
collagen for its lifeline. What could the mechanical consequences of this
helix destabilization be on the thread compared with traditional fibrillar
collagens and what benefits might it offer for the mussel? At present, there
are no answers to these questions.
Histidine-rich domain
Histidine containing sequences in the N- and C-termini resembling known
metal-binding motifs (Papallardo et al., 2002) are highly conserved between
all three species, implying a functional role for these sequences, possibly as
cross-link participants. The conservation of His-rich domains between M.
californianus and the other two species was unexpected in light of their
mechanical differences in the distal region. Self-healing is believed to be
the result of the reformation of histidine–metal coordination bonds
sacrificially broken during yield, and since M. californianus
exhibits significantly faster recovery of stiffness and hysteresis, it has
been proposed that it might have significant differences in the histidine-rich
regions (Lucas et al., 2002).
Even where it is not entirely conserved, there is no trend that would favor
M. californianus as a faster healer. The fact that this region is not
significantly different in M. californianus does not exclude the
His–metal interaction as the reversibly breakable bond responsible for
recovery, but instead suggests that there may be a separate force driving
these bonds back together and that this force is different between species,
resulting in different rates of healing. This requires a separate elastomeric
component in parallel with the His-rich domain and possible candidates are
proposed at the end of the Discussion.
Mechanical testing
In order to correlate our sequence homology data with the mechanical data,
we must make several assumptions. First, we assume that threads are composed
entirely of preCols and that they alone determine the mechanical properties.
This assumption seems reasonable for the distal region considering that preCol
D and NG make up 96% of the protein component. Second, we assume that the
molecular packing is similar between species, and that any differences in
architecture play a minor role in mechanical differences. Since the overall
domain structure of the preCols has been shown to be similar in all species,
it is a safe assumption that the preCols of M. californianus maintain
a similar smectic alignment as threads of M. galloprovincialis
(Hassenkam et al., 2004).
Mechanical testing of threads performed in this study revealed that in
native seawater-treated distal threads, no modulus reduction and low
hysteresis are seen between 0–10% strain
(Fig. 7). Stress softening
occurs once threads yield (16% strain) and continues until about 40%
strain. However, this softening is reversible in a time-dependent manner
(Carrington and Gosline, 2004).
Histidine–metal interactions are the ideal candidate for a sacrificial
cross-link since they are known to break and reform reversibly and are
significantly weaker than covalent bonds
(Schmitt et al., 2000). Due to
consistent conservation of abundant histidine compositions in the preCol
termini, the presence of metals in elevated levels in the thread core
(Coombs and Keller, 1981), and
the loss of yield and recovery in EDTA-treated threads in which about 50% of
the metal was removed (Vaccaro and Waite,
2001), we believe these cross-links function mechanically in
mussel byssal threads.
To further probe the role of histidine in mechanical performance, threads
were exposed to citrate-phosphate buffer at pH 3, 4, 5, 6, 7 and 8 prior to
mechanical testing. The local pH dictates the degree of protonation of
histidine within this range since the pKa of a protein histidyl
residue is 6.5 (Sundberg and Martin,
1974). Protonation of histidine gives the side chain a positive
charge, preventing it from binding metal
(Fig. 2). Since pH treatment
can be used to control the degree of protonation and consequently the density
of metal cross-links within the thread, we predict that treatment at low pH
will adversely affect the mechanical performance. Histidine is the only amino
acid side chain that will undergo a complete dissociation between pH 3 and 8
so we can be reasonably confident that the acidic pH treatment is primarily
targeting these residues.
As Fig. 8 reveals, the initial modulus of threads over the pH range traces a roughly sigmoidal shape with a midpoint around 615 MN m–2 corresponding to pH 6.6. As mentioned, this pH is significant since the pKa of histidine usually falls in this range and at the pKa you would expect 50% of the histidine residues protonated and unable to bind metals and 50% deprotonated and bound in metal coordination crosslinks. Since the halfway point of the modulus reduction between pH 3 and 8 falls at this particular pH, it is very suggestive that His–metal bonds are serving as cross-links against tensile stress.
The loss in stiffness from low pH treatment is completely reversible by re-equilibrating the low pH thread in buffer at pH 8. This is consistent with pH-mediated disruption of His–metal cross-links, which would be completely reversible as long as some metal remains in solution. This reversibility can be prevented by treating threads with DEPC at an acidic pH, trapping unbound, deprotonated histidine residues in a carbethoxylated state where they are unable to participate in coordinate bonds (Fig. 2), and thus maintaining threads at lower stiffness even after the pH is returned to 8.
Fig. 9A reveals that at low strain values, there is a large difference in stiffness between threads treated at pH 8 and pH 5 that becomes less prominent the more the thread is strained. Fig. 9B reveals that below yield and above 40% strain the magnitude of stress softening after each strain cycle between pH 8- and pH 5-treated threads is not significantly different, but between the onset of yield and 40% strain they are. If the only difference between threads equilibrated to pH 5 and pH 8 is their respective density of His–metal cross-links, the implication arises that these bonds are not broken before yield and are fully sacrificed by around 40% strain. It should be noted that threads treated at acidic pH still show a measure of yield and stress-softening, just to a smaller degree (Fig. 9A,B). It is possible that not all His–metal cross-links were disrupted, but this seems unlikely, especially at pH 3. More plausibly, the histidine residues are not the only source of reversibly breakable bonds in the threads and these other bonds are not affected by the pH change from 3 to 8. A possible candidate for the pH-independent reversible elasticity is the Gly-rich flank of preCol NG. This will be amplified in the molecular model below.
|
Model
Prior to yield, His–metal interactions bridge the ends of a series of
preCols, allowing the stiff flanking and collagen domains to dominate
stress–strain behavior. At this point recovery is essentially elastic
with high resilience, and initial stiffness is a function of stiffness of the
flanking domains. At yield, stress on the domains of the preCol reaches a
critical level that exceeds the load capacity of the His–metal
coordinate bonds and they begin to rupture, dissipating the applied energy in
the form of molecular friction (hysteresis). In sacrificing His–metal
complexes, the covalent bonds in the backbone are spared and catastrophic
failure is avoided. This may also be the point at which the non-His
sacrificial bonds begin to rupture since yield, stress softening, and
hysteresis are also seen in low pH threads. The best candidates for these are
the NG flanks which, with a predicted amorphous structure, are likely to be
more compliant than the collagen cores and the Ala-rich silk-like flanks.
Beyond 40% strain, most His–metal bonds are broken, and further stress
softening (which is small) is not due to the His–metal bonds breaking.
Evidence for this comes from the fact that E is not
significantly different between high pH and low pH above 40% strain.
Since coordinate bonds are known to be reversibly breakable, His–metal could play a role in post-yield recovery if the separated ligands and metals are brought together again. His domains are not different between species, and as M. californianus is a faster healer, differences in recovery rate must come from another source. This suggests the presence of separate elastomeric components in parallel with the histidine-rich domains, which restore them after deformation. The flanking domains of NG are again the best candidates as the restoring elastomeric component. Since preCol D and NG are both known to be present in the distal region of the thread and since the preCols are believed to assemble in register, a composite model of yield and self-healing is outlined in Fig. 10. In this model, the stiffness of the flanking domains of NG and of the His-rich domains in D are roughly comparable. Both begin to break near the critical yield stress. When the applied load is released, the flanking regions of NG recover entropically, dragging the separated histidine residues between two preCol Ds back into mutual proximity and thus restore their metal coordination.
The assumed entropic recovery of NG flanks is an important component of our
model and deserves closer scrutiny in future experimental studies. It has been
proposed that Gly-rich proteins in plant cell walls homologous to those in NG
flanking domains form a loose structure known as a glycine loop, reminiscent
of keratin termini (Steinert et al.,
1991). Glycine loops are believed to behave like molecular
VELCROTM, in which the ordered structure is easily disrupted
by moderate tension, but is able to recover its initial conformation after
stress is released (Sachetto-Martins et
al., 2000). This sort of moderately stiff, entropic elastic
component would be a good fit as the component driving recovery.
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Acknowledgments |
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References |
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TOPSummaryIntroductionMaterials and methodsResultsDiscussionReferences |
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