Major Ampullate Gland Research Articles

Spider silk protein refolding is controlled by changing pH.

Spidroins, the major silk proteins making up the spider's dragline silk, originate in two distinct tissue layers (A and B) in the spider's major ampullate gland. Formation of the complex thread from spidroins occurs in the lumen of the duct connected to the gland. Using pH-sensitive microelectrode probes, we showed that the spidroins traveling through the gland and duct experience a monotonic decrease in pH from 7.2 to 6.3. In addition, circular dichroism spectroscopy of material extracted from the gland showed a structural refolding concomitant with position in the gland and post-extraction changes in pH. We demonstrate that lowering the pH in vitro causes a dramatic conformational change in the protein from the A zone, converting it irreversibly from a coil to a predominantly beta-sheet structure. Furthermore, amino acid analyses have indicated that there are at least two distinct, though similar, proteins secreted in the A and B zones suggesting a potential factor in the progressive acidification as well as a pH sensitivity of the folding of spidroins in the gland. Thus, we provide, for the first time, a quantitative map of the pH value and position correlated with molecular structural folding in the silk gland characterizing the crucial role that pH plays in spider silk formation.

Structural conformation of spidroin in solution: a synchrotron radiation circular dichroism study.

Spider silk is made and spun in a complex process that tightly controls the conversion from soluble protein to insoluble fiber. The mechanical properties of the silk fiber are modulated to suit the needs of the spider by various factors in the animal's spinning process. In the major ampullate (MA) gland, the silk proteins are secreted and stored in the lumen of the ampulla. A particular structural fold and functional activity is determined by the spidroins' amino acid sequences as well as the gland's environment. The transition from this liquid stage to the solid fiber is thought to involve the conversion of a predominantly unordered structure to a structure rich in beta-sheet as well as the extraction of water. Circular dichroism provides a quick and versatile method for examining the secondary structure of silk solutions and studying the effects of various conditions. Here we present the relatively novel technique of synchrotron radiation based circular dichroism as a tool for investigating biomolecular structures. Specifically we analyze, in a series of example studies on structural transitions induced in liquid silk, the type of information accessible from this technique and any artifacts that might arise in studying self-assembling systems.

Consequences of forced silking.

The forced silking of a spider to obtain major ampullate (MA) silk for experiments is a standard practice; however, this method may have profound effects on the resulting silk's properties. Experiments were performed to determine the magnitude of the difference in the forces required to draw silk from the MA gland between unrestrained spiders descending on their draglines and restrained spiders from which MA silk was drawn with a motor. The results show that freely falling spiders can spool silk with as little as 0.1 body weights of force, which generates a stress that is about 2% of the silk's tensile strength. In contrast, forcibly silked spiders apply as much as 4 body weights of force with an internal braking mechanism, and this force creates silk stresses in excess of 50% of the silk's tensile strength. The large forces observed in forced silking should strongly affect the draw alignment of the polymer network in the newly spun fibers, and this may account for the differences in material properties observed between naturally spun and forcibly spun MA silks. In addition, the heat produced by the internal friction brake during forced silking may set the upper limit of forced silking speed.

NMR characterization of native liquid spider dragline silk from Nephila edulis.

Solid spider dragline silk is well-known for its mechanical properties. Nonetheless a detailed picture of the spinning process is lacking. Here we report NMR studies on the liquid silk within the wide sac of the major ampullate (m.a.) gland from the spider Nephila edulis. The resolution in the NMR spectra is shown to be significantly improved by the application of magic-angle spinning (MAS). From the narrow width of the resonance lines and the chemical shifts observed, it is concluded that the silk protein within the wide sac of the m.a. gland is dynamically disordered throughout the molecule in the sense that each amino acid of a given type senses an identical environment, on average. The NMR data obtained are consistent with an isotropic liquid phase.

Conserved C-termini of Spidroins are secreted by the major ampullate glands and retained in the silk thread.

The C-termini of Spidroins produced in the major and minor ampullate glands of spiders are highly conserved. Despite this conservation, no corresponding peptides have been identified in the spinning dopes or the silk filaments so far. To prove their presence or absence, polyclonal antibodies derived against fusion proteins containing the conserved C-terminal regions of both Spidroin 1 and 2 from the spider Nephila clavipes were generated. The antibodies reacted with high molecular weight polypeptides of the corresponding gland extracts and solubilized major ampullate filament and in addition to filament cross-sections. This demonstrates the existence of C-terminal specific peptides in the spinning dope and the mature Spidroins. Both the fusion proteins as well as the proteins contained within the gland lumen showed a reduction in their size under reducing conditions indicating the presence of disulfide bonds. Their high conservation and the biochemical data suggest crucial roles the C-termini play in the formation and/or structure of the corresponding silk filaments.

Supercontraction Stress in Spider Webs

Silk produced from the major ampullate (MA) gland supercontracts when wet, and in this paper, we investigate the consequences of high humidity and of the added load of water droplets condensing from saturated air on the mechanical integrity of the spiders' orb web. We measured the development of the supercontraction stress (sigma(sc)) with time when fixed lengths of MA silk from Nephila clavipes and Argiope aurantia were exposed to increasing humidity. Supercontraction generated stresses of about 50 MPa, and extension of these samples to stresses between 150 and 1100 MPa show a time dependent relaxation over 1000 s to approximately 75% of the initial tension but show no indication of failure. We conclude that supercontraction can maintain tension in webs and does not limit the ability of the web to support loads in excess of the supercontraction stress.

ON THE USE OF AMPULLATE GLAND SILKS BY WOLF SPIDERS (ARANEAE, LYCOSIDAE) FOR ATTACHING THE EGG SAC TO THE SPINNERETS AND A PROPOSAL FOR DEFINING NUBBINS AND TARTIPORES

Abstract The means by which female wolf spiders attach an egg sac to their spinnerets was investigated using scanning electron microscopy. In four Pardosa species, we observed that silk fibers emerging from ampullate gland spigots had been affixed to the surface of the egg sac. More specifically, primary (1°) and secondary (2°) major ampullate (MaA) glands and 1° and 2° minor ampullate (MiA) glands all contributed fibers for this purpose. The diameters of the 2° MaA and 2° MiA fibers were greater than those of the 1° MaA and 1° MiA fibers and, correspondingly, the widths of the 2° ampullate spigots were clearly greater than those of the 1° ampullate spigots. Larger 2° ampullate spigots were also observed in adult females of species from three other lycosid genera. Thus, 2° ampullate glands, which in araneoids function only in juveniles during proecdysis, are not only functional in adult female lycosids (and adult females of several other families), but they appear to play a greater role than the 1° ampull...

Elastic theory of single spider silk protein molecule

Spider silk exhibits two excellent mechanical features, toughness and extensibility. In recent years, considerable investigations have been focused on it. The understanding of spider silk protein is significant for the bionic silk. In this article, we study the force extension property of spider silk proteins as the function of the amino acid compositions for major and minor ampullate glands of typical Araneid orb weaver, as well as one artificial spider silk by Monte Carlo simulation. The results are also compared with a designed protein whose amino acid composition is uniform. It shows clearly that the major and minor ampullate gland proteins are much tougher than the designed protein, and the artificial protein as a model of a nature spider silk do have good mechanical properties. Our simulation reveals that the mechanical property of a spider silk protein is dependent on amino acid composition and the composition of spider silk protein is an excellent result of natural evolution.

From EST sequence to spider silk spinning: identification and molecular characterisation of Nephila senegalensis major ampullate gland peroxidase NsPox

Spider dragline silk is renowned as one of the toughest materials of its kind. In nature, spider silks are spun out of aqueous solutions under environmental conditions. This is in contrast to production of most synthetic fibres, where hazardous solvents, high temperatures and pressure are used. In order to identify some of the chemical processes involved in spider silk spinning, we have produced a collection of cDNA sequences from specific regions of Nephila senegalensis major ampullate gland. We examined in detail the sequence and expression of a putative Nephila senegalensis peroxidase gene ( NsPox) from our EST collection. NsPox encodes a protein with similarity to Drosophila melanogaster and Aedes aegypti peroxidases. Northern analysis and in situ localisation experiments revealed that NsPox is expressed in major and minor ampullate glands of the spider where the main components of the dragline silk are produced. We suggest that NsPox plays a role in dragline silk fibre formation and/or processing.

Ultrastructure of the major ampullate gland of the black widow spider, Latrodectus hesperus

Silk production in the spider occurs within specialized glands that are capable of the synthesis of large fibrous proteins and the post-translational processing of those proteins to form an insoluble fiber. The major ampullate gland of Latrodectus hesperus (black widow) is similar in morphology to those found in the Araneid spiders. The tail domain of this gland is highly protein synthetic, giving rise to a core, fibrous protein product. In addition to a storage function, the ampulla region also synthesizes and exports an electron dense material that appears to form a ‘coat’ surrounding the silk generated within the tail. The duct of the gland consists of at least two distinct cell types: one type contains ‘honeycomb’ vesicles of unknown function, while the other possesses elaborate apical microvilli that may be involved in the reabsorption of water and subsequent dehydration of the silk. As the silk product transits through these various stages of assembly, it can been seen to undergo a condensation or concentration, possibly reflecting the influence of both the shear forces induced by movement into the duct and the dehydration that is thought to occur there.

Spinning an elastic ribbon of spider silk.

The Sicarid spider Loxosceles laeta spins broad but very thin ribbons of elastic silk that it uses to form a retreat and to capture prey. A structural investigation into this spider's silk and spinning apparatus shows that these ribbons are spun from a gland homologous to the major ampullate gland of orb web spiders. The Loxosceles gland is constructed from the same basic parts (separate transverse zones in the gland, a duct and spigot) as other spider silk glands but construction details are highly specialized. These differences are thought to relate to different ways of spinning silk in the two groups of spiders. Loxosceles uses conventional die extrusion, feeding a liquid dope (spinning solution) to the slit-like die to form a flat ribbon, while orb web spiders use an extrusion process in which the silk dope is processed in an elongated duct to produce a cylindrical thread. This is achieved by the combination of an initial internal draw down, well inside the duct, and a final draw down, after the silk has left the spigot. The spinning mechanism in Loxosceles may be more ancestral.

Chummidae, a new spider family (Arachnida, Araneae) from South Africa

AbstractThe paper reports on a new family of spiders from the eastern Cape region in South Africa. Chummidae, new family, are small, three‐clawed spiders, recognized by the abdomen with strong dorsal scutum, provided with a frontal field of stiff macrosetae in large sockets. Further apomorphies are the absence of a fovea, the reduction of posterior and median spinnerets, the absence of major ampullate gland spigots, and the presence of branched lateral tracheae and of a hair‐basket around the cheliceral fang. The type genus Chumma, is represented by two species, both known from male and female – the type species C. inquieta sp. nov. and C. gastroperforata sp. nov. The males of the latter species are remarkable for having two pairs of abdominal pockets, which play a role during mating.

Supercontraction and Backbone Dynamics in Spider Silk: 13C and 2H NMR Studies

The high-performance mechanical properties of certain spider silks can be radically altered by the addition of water. For example, unconstrained silk fibers from the major ampullate gland of the golden orb-weaving spider, Nephila clavipes, contract to about half of their original length when immersed in water. In this paper we use solid-state 13C and 2H NMR to study N. clavipes silk fibers, so as to address the molecular origins of supercontraction in the wet silk. Using 13C NMR, we study backbone dynamics and demonstrate that, when in contact with water, a substantial fraction of the glycine, glutamine, tyrosine, serine, and leucine residues in the protein backbone show dramatic increases in the rate of large-amplitude reorientation. 2H NMR of silk samples that incorporate leucine deuterated at one terminal methyl group provides a probe for dynamics at specific side chains along the fiber. Only a subset of these leucine residues is strongly affected by water. We suggest that the highly conserved YGGLGS(N)QGAGR blocks found in the silk protein play a major role in the supercontraction process. Amino acid sequences are proposed to produce artificial spider silk with similar mechanical properties, but without the undesired phenomenon of supercontraction. A possible use of the “supercontracting sequence” is also suggested.

Glycoproteins and skin-core structure in Nephila clavipes spider silk observed by light and electron microscopy.

Microscopical imaging of natural, unstressed draglines or of untreated bulk samples showed two types or threads with diameters of either approximately 1-2 microm or 4-5 microm, which could be identified as products of the minor or major ampullate glands. The threads had a circular profile in serial cross sections and are surrounded by a thin outer layer of a different material within the section. Such fibrillar configurations were also found in untreated threads or in the same serial sections of transmission electron microscopy (TEM) samples by means of the special technique of laser scanning microscopy. In TEM slides, numerous cavities with the same circular profile were detectable, and the length of these cavities is variable from 40-300 nm. The threads are oriented parallel and twisted around themselves to construct a double thread. In the interface between the two single threads, bridge-like structures are prominent. The single untreated thread consists of cylindrical fibers with a diameter of approximately 1-1.5 microm. Apparently more than eight fibers are within a thread and each fiber is composed of a great number of fibrils with a diameter of about 150 nm. The surface of threads is coated with a characteristic layer approximately 150-250 nm thick that contains glycoproteins. These were demonstrated for the first time by labeling with concanavalin A lectin-gold complex and are dependent on the diameter and length of the thread. The same substances could also be detected inside the single thread. The skin can be removed completely or partially by mechanical treatment, or by washing with phosphate-buffered saline or trypsin.

The mechanical design of spider silks: from fibroin sequence to mechanical function.

Spiders produce a variety of silks, and the cloning of genes for silk fibroins reveals a clear link between protein sequence and structure-property relationships. The fibroins produced in the spider's major ampullate (MA) gland, which forms the dragline and web frame, contain multiple repeats of motifs that include an 8-10 residue long poly-alanine block and a 24-35 residue long glycine-rich block. When fibroins are spun into fibres, the poly-alanine blocks form (&bgr;)-sheet crystals that crosslink the fibroins into a polymer network with great stiffness, strength and toughness. As illustrated by a comparison of MA silks from Araneus diadematus and Nephila clavipes, variation in fibroin sequence and properties between spider species provides the opportunity to investigate the design of these remarkable biomaterials.

Liquid crystals and flow elongation in a spider's silk production line

Our observations on whole mounted major ampullate silk glands suggested that the thread is drawn from a hyperbolic die using a pre–orientated lyotropic liquid crystalline feedstock. Polarizing microscopy of the gland's duct revealed two liquid crystalline optical textures: a curved pattern in the feedstock within the ampulla of the gland and, later in the secretory pathway, the cellular texture previously identified in synthetic nematic liquid crystals. The behaviour of droplet inclusions within the silk feedstock indicated that elongational flow at a low shear rate occurs in the gland's duct and may be important in producing an axial molecular orientation before the final thread is drawn. Our observations suggested that the structure of the spider's silk production pathway and the liquid crystalline feedstock are both involved in defining the exceptional mechanical properties of spider dragline silk.

Structure and function of the silk production pathway in the Spider Nephila edulis

Our observations on the major ampullate gland of the spider Nephila edulis indicate that the exceptionally tough and strong core and coat composite structure of the dragline thread is formed by the co-drawing of two feedstocks through a single die. The cuticle that lines the gland’s duct has the structure of an advanced hollow fibre dialysis membrane and is thought to facilitate a rapid removal of water and change in ionic composition involved in the spinning process. A structure previously termed the ‘valve’ is thought to advance the broken thread and act as a pump to restart spinning after the accidental internal rupture of a thread. Together, these observations indicate that the spider silk production pathway is highly optimised for the production of silk threads and shows considerable biomimetic potential.

Purification and characterization of recombinant spider silk expressed in Escherichia coli.

A partial cDNA clone, from the 3' end of the dragline silk gene was isolated from Nephila clavipes major ampullate glands. This clone contains a 1.7-kb insert, consisting of a repetitive coding region of 1.4-kb and a 0.3-kb nonrepetitive coding region; 1.5-kb of the 1.7-kb fragment was cloned into Escherichia coli and a 43-kDa recombinant silk protein was expressed. Characterization of the purified protein by Western blot, amino acid composition analysis, and matrix-assisted laser desorption ionization/time-of-flight mass spectrometry confirms it to be spider dragline silk.

Rotational-echo double-resonance in complex biopolymers: a study of Nephila clavipes dragline silk.

Rotational-Echo Double-Resonance (REDOR) NMR on strategically 13C and 15N labeled samples is used to study the conformation of the LGXQ (X = S, G, or N) motif in the major ampullate gland dragline silk from the spider Nephila clavipes. A method is described for calculating REDOR dephasing curves suitable for background subtractions, using probability distributions of nitrogen atoms surrounding a given carbon site, which are developed from coordinates in the Brookhaven Protein Data Bank. The validity of the method is established by comparison to dephasings observed from natural abundance 13C peaks for G and A. Straightforward fitting of universal REDOR dephasing curves to the background corrected peaks of interest provides results which are not self-consistent, and a more sophisticated analysis is developed which better accounts for 15N labels which have scrambled from the intended positions. While there is likely some heterogeneity in the structures formed by the LGXQ sequences, the data indicate that they all form compact turn-like structures.

Small-Angle X-ray Scattering of Spider Dragline Silk

As part of a general study of the structure of spider silk fibers, major ampullate gland silk fibers were collected from Nephila clavipes spiders, and SAXS patterns were obtained from loops of fibers under a variety of conditions. Two orders of lamellar reflection were seen, with a long spacing of 8.4 nm. This increased reversibly by 4% when the fiber was stretched by 10% and shrank to 5.8 nm when the fiber itself shrank 45% on wetting. A strong equatorial streak had a bimodal orientation distribution similar to that seen in NMR and WAXD. The sharper component had a lateral size scale (radius of gyration) of 2.5 nm and a misorientation of 10° FWHM, similar to the orientation of the crystals. The minimum breadth of the streak indicates that the scattering objects are 0.1 μm long. There is an isotropic central scattering, probably caused by voids. On wetting, the lamellar peaks became more intense; more dramatically, the equatorial scattering strengthens and extends to higher angles, almost halving the lateral size scale to 1.4 nm. An equatorial maximum appears at a spacing of 6 nm, indicating a degree of order in the fibrillar structure.