Physics:Spider silk

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Short description: Protein fiber made by spiders


A female specimen of Argiope bruennichi wraps her prey in silk.
Indian Summer by Józef Chełmoński (1875, National Museum in Warsaw) depicts a peasant woman with a thread of gossamer in her hand.
Spider cocoon

Spider silk is a protein fibre or silk spun by spiders. Spiders use silk to make webs or other structures that function as adhesive traps to catch prey, to entangle and restrain prey before biting, to transmit tactile information, or as nests or cocoons to protect their offspring. They can use the silk to suspend themselves from height, to float through the air, or to glide away from predators. Most spiders vary the thickness and adhesiveness of their silk according to its use.

In some cases, spiders may use silk as a food source.[1] While methods have been developed to collect silk from a spider by force,[2] gathering silk from many spiders is more difficult than from silk-spinning organisms such as silkworms.

All spiders produce silk, although some spiders do not make webs. Silk is tied to courtship and mating. Silk produced by females provides a transmission channel for male vibratory courtship signals, while webs and draglines provide a substrate for female sex pheromones. Observations of male spiders producing silk during sexual interactions are common across widespread taxa. The function of male-produced silk in mating has received little study.[3]

Properties

Structural

Structure of spider silk. Inside a typical fibre there are crystalline regions separated by amorphous linkages. The crystals are beta-sheets that have assembled together.

Silks, have a hierarchical structure. The primary structure is the amino acid sequence of its proteins (spidroin), mainly consisting of highly repetitive glycine and alanine blocks,[4][5] which is why silks are often referred to as a block co-polymer. On a secondary level, the short side-chained alanine is mainly found in the crystalline domains (beta sheets) of the nanofibril. Glycine is mostly found in the so-called amorphous matrix consisting of helical and beta turn structures.[5][6] The interplay between the hard crystalline segments and the strained elastic semi-amorphous regions gives spider silk its extraordinary properties.[7][8] Various compounds other than protein are used to enhance the fibre's properties. Pyrrolidine has hygroscopic properties that keep the silk moist while warding off ant invasion. It occurs in high concentration in glue threads. Potassium hydrogen phosphate releases hydrogen ions in aqueous solution, resulting in a pH of about 4, making the silk acidic and thus protecting it from fungi and bacteria that would otherwise digest the protein. Potassium nitrate is believed to prevent the protein from denaturing in the acidic milieu.[9]

Termonia introduced this first basic model of silk in 1994.[10] He suggested crystallites embedded in an amorphous matrix interlinked with hydrogen bonds. Refinements to this model include: semi-crystalline regions were found[5] as well as a fibrillar skin core model suggested for spider silk,[11] later visualised by AFM and TEM.[12] Sizes of the nanofibrillar structure and the crystalline and semi-crystalline regions were revealed by neutron scattering.[13]

The fibres' microstructural information and macroscopic mechanical properties are related.[14] Ordered regions (i) mainly reorient by deformation for low-stretched fibres and (ii) the fraction of ordered regions increases progressively for higher fibre stretching.


Mechanical

Each spider and each type of silk has a set of mechanical properties optimised for their biological function.

Most silks, in particular dragline silk, have exceptional mechanical properties. They exhibit a unique combination of high tensile strength and extensibility (ductility). This enables a silk fibre to absorb a large amount of energy before breaking (toughness, the area under a stress-strain curve).

An illustration of the differences between toughness, stiffness and strength

Strength and toughness are distinct quantities. Weight for weight, silk is stronger than steel, but not as strong as Kevlar. Spider silk is, however, tougher than both.

The variability of spider silk fibre mechanical properties is related to their degree of molecular alignment.[16] Mechanical properties also depend on ambient conditions, i.e. humidity and temperature.[17]

Strength

A dragline silk's tensile strength is comparable to that of high-grade alloy steel (450−2000 MPa),[18][19] and about half as strong as aramid filaments, such as Twaron or Kevlar (3000 MPa).[20]

Density

Consisting of mainly protein, silks are about a sixth of the density of steel (1.3 g/cm3). As a result, a strand long enough to circle the Earth would weigh about 2 kilograms (4.4 lb). (Spider dragline silk has a tensile strength of roughly 1.3 GPa. The tensile strength listed for steel might be slightly higher – e.g. 1.65 GPa,[21][22] but spider silk is a much less dense material, so that a given weight of spider silk is five times as strong as the same weight of steel.)

Energy density

The energy density of dragline spider silk is roughly 1.2×108 J/m3.[23]

Ductility

Silks are ductile, with some able to stretch up to five times their relaxed length without breaking.

Toughness

The combination of strength and ductility gives dragline silks a high toughness (or work to fracture), which "equals that of commercial polyaramid (aromatic nylon) filaments, which themselves are benchmarks of modern polymer fibre technology".[24][25]

Temperature

While unlikely to be relevant in nature, dragline silks can hold their strength below -40 °C (-40 °F) and up to 220 °C (428 °F).[26] As occurs in many materials, spider silk fibres undergo a glass transition. The glass-transition temperature depends on humidity, as water is a plasticiser for spider silk.[17]

Supercontraction

When exposed to water, dragline silks undergo supercontraction, shrinking up to 50% in length and behaving like a weak rubber under tension.[17] Many hypotheses have attempted to explain its use in nature, most popularly to re-tension webs built in the night using the morning dew.[citation needed]

Highest-performance

The toughest known spider silk is produced by the species Darwin's bark spider (Caerostris darwini): "The toughness of forcibly silked fibers averages 350 MJ/m3, with some samples reaching 520 MJ/m3. Thus, C. darwini silk is more than twice as tough as any previously described silk and over 10 times tougher than Kevlar".[27]

Adhesive

Silk fibre is a two-compound pyriform secretion, spun into patterns (called "attachment discs") using a minimum of silk substrate.[28] The pyriform threads polymerise under ambient conditions, become functional immediately, and are usable indefinitely, remaining biodegradable, versatile and compatible with other materials in the environment.[28] The adhesive and durability properties of the attachment disc are controlled by functions within the spinnerets.[29] Some adhesive properties of the silk resemble glue, consisting of microfibrils and lipid enclosures.[28]

Uses

All spiders produce silks, and a single spider can produce up to seven different types of silk for different uses.[30] This is in contrast to insect silks, where an individual usually only produces a single type.[31] Spiders use silks in many ways, in accord with the silk's properties. As spiders have evolved, so has their silks' complexity and uses, for example from primitive tube webs 300–400 million years ago to complex orb webs 110 million years ago.[32]

Use Example Reference
Prey capture Orb webs produced by the Araneidae (typical orb-weavers); tube webs; tangle webs; sheet webs; lace webs, dome webs; single thread used by the Bolas spiders for "fishing". [30][32]
Prey immobilisation "Swathing bands" to envelop prey. Often combined with immobilising prey using a venom. In species of Scytodes the silk is combined with venom and squirted from the chelicerae. [30]
Reproduction Male spiders may produce sperm webs; spider eggs are covered in silk cocoons. [30][33]
Dispersal "Ballooning" or "kiting" used by smaller spiders to float through the air, for instance for dispersal. [34]
Food The kleptoparasitic Argyrodes eats the silk of host spider webs. Some daily weavers of temporary webs eat their own unused silk, thus mitigating an otherwise heavy metabolic expense. [1][35]
Nest lining and nest construction Tube webs used by "primitive" spiders such as the European tube web spider (Segestria florentina). Threads radiate out of the nest to provide a sensory link to the outside. Silk is a component of the lids of spiders that use "trapdoors", such as members of the family Ctenizidae, and the "water" or "diving bell" spider Argyroneta aquatica forms a silk diving bell. [32]
Guide lines Some spiders that venture from shelter leave a silk trail by which to find their way home again. [35]
Drop lines and anchor lines Spiders such as the Salticidae venture from shelter and leave a trail of silk, use that as an emergency line in case of falling from inverted or vertical surfaces. Others, even web dwellers, deliberately drop from a web when alarmed, using a silken thread as a drop line by which they can return in due course. Some, such as species of Paramystaria, hang from a drop line while feeding. [35]
Alarm lines Some spiders that do not spin actual trap build alarm webs that the feet of their prey (such as ants) can disturb, cueing the spider to pounce on prey or flee a formidable intruder. [35]
Pheromonal trails Some wandering spiders leave a largely continuous trail of silk impregnated with pheromones that the opposite sex can follow to find a mate. [35]

Silk types

right|thumb|A female Argiope picta immobilizing prey by wrapping a curtain of aciniform silk around the insect for later consumption Meeting the specification for all these ecological uses requires different types of silk presenting different properties, as either a fibre, a structure of fibres, or a globule. These types include glues and fibres. Some types of fibres are used for structural support, others for protective structures. Some can absorb energy effectively, whereas others transmit vibration efficiently. These silk types are produced in different glands; so the silk from a particular gland can be linked to its use.

Gland Silk Use
Ampullate (major) Dragline silk – used for the web's outer rim and spokes, also for lifeline and for ballooning
Ampullate (minor) Used for temporary scaffolding during web construction
Flagelliform Capture-spiral silk – used for the capturing lines of the web
Tubuliform Egg cocoon silk – used for egg sacs
Aciniform Used to wrap and secure prey; used in male sperm webs; used in stabilimenta
Aggregate Sticky globules
Piriform Bonds between separate threads for attachment point.

Many species have different glands to produce silk with different properties for different purposes, including housing, web construction, defence, capturing and detaining prey, egg protection, and mobility (fine "gossamer" thread for ballooning, or for a strand allowing the spider to drop down as silk is extruded).[36][37]

Silk Use
Major-ampullate (dragline) silk The web's outer rim and spokes and the lifeline. Can be as strong per unit weight as steel, but much tougher.
Capture-spiral (flagelliform) silk Capturing lines. Sticky, stretchy, and tough. The capture spiral is sticky due to droplets of aggregate (a spider glue) that are placed on the spiral. The elasticity of flagelliform allows enough time for the aggregate to adhere to the aerial prey flying into the web.
Tubiliform (a.k.a. cylindriform) silk Protective egg sacs. Stiffest silk.
Aciniform silk Wrap and secure prey. Two to three times as tough as the other silks, including dragline.
Minor-ampullate silk Temporary scaffolding during web construction.

Synthesis and fibre spinning

A garden spider spinning its web

Silk production differs in an important aspect from that of most other fibrous biomaterials. It is pulled on demand from a precursor out of specialised glands,[38] rather than continuously grown like plant cell walls.[23]

The spinning process occurs when a fibre is pulled away from the body of a spider, whether by the spider's legs, by the spider's falling under its own weight, or by any other method. The term "spinning" is misleading because no rotation occurs. It comes from analogy to the textile spinning wheels. Silk production is a pultrusion,[39] similar to extrusion, with the subtlety that the force is induced by pulling at the finished fibre rather than squeezing it out of a reservoir. The fibre is pulled through (possibly multiple) silk glands of multiple types.[38]

Silk gland

Schematic of the spiders spinning apparatus and structural hierarchy in silk assembling related to assembly into fibers.[40][41][42][43][44] In the process of dragline production, the primary structure protein is secreted first from secretory granules in the tail.[45] In the ampullate (neutral environment, pH = 7), the proteins form a soft micelle of several tens of nanometers by self-organization because the hydrophilic terminals are excluded.[46] In ampullate, the concentration of the protein is high.[47][48] Then, the micelles are squeezed into the duct. The long axis direction of the molecules is aligned parallel to the duct by a mechanical frictional force and partially oriented.[45][46][49] The continuous lowering of pH from 7.5 to 8.0 in the tail to presumably close to 5.0 occurs at the end of the duct.[41][50][51] Ion exchange, acidification, and water removal all happen in the duct.[42] The shear and elongational forces lead to phase separation.[42] In the acidic bath of the duct, the molecules attain a high concentration liquid crystal state.[52] Finally, the silk is spun from the taper exterior. The molecules become more stable helixes and β-sheets from the liquid crystal.

The gland's visible, or external, part is termed the spinneret. Depending on the complexity of the species, spiders have two to eight spinnerets, usually in pairs. Species have varying specialised glands, ranging from a sac with an opening at one end, to the complex, multiple-section ampullate glands of the golden silk orb-weavers.[53]

Behind each spinneret on the surface of the spider lies a gland, a generalised form of which is shown in the figure.

Gland characteristics
Schematic of a generalised gland of a Golden silk orb-weaver. Each differently coloured section highlights a discrete section of the gland.[54][55]
  1. The leftmost section s the secretory or tail section. The walls of this section are lined with cells that secrete proteins Spidroin I and Spidroin II, the main components of this spider's dragline. These proteins are found in the form of droplets that gradually elongate to form long channels along the length of the final fibre, hypothesised to assist in preventing crack formation or self-healing.[56]
  2. The ampulla (storage sac) is next. This stores and maintains the gel-like unspun silk dope. In addition, it secretes proteins that coat the surface of the final fibre.[24]
  3. The funnel rapidly reduces the large diameter of the storage sac to the small diameter of the tapering duct.
  4. The final length is the tapering duct, the site of most of the fibre formation. This consists of a tapering tube with several tight sharp turns, a valve near the end includes a spigot from which the solid silk fibre emerges. The tube tapers hyperbolically, therefore the unspun silk is under constant elongational shear stress, an important factor in fibre formation. This section is lined with cells that exchange ions, reduce the dope pH from neutral to acidic, and remove water from the fibre.[57] Collectively, the shear stress and the ion and pH changes induce the liquid silk dope to undergo a phase transition and condense into a solid protein fibre with high molecular organisation. The spigot at the end has lips that clamp around the fibre, controlling fibre diameter and further retaining water.
  5. Almost at the end is a valve. Though discovered some time ago, its precise purpose is still under discussion. It is believed to assist in restarting and rejoining broken fibres,[58] acting much in the way of a helical pump, regulating the thickness of the fibre,[39] and/or clamping the fibre as a spider falls upon it.[58][59] The similarity of the silk worm's silk press and the roles each of these valves play in the silk production in these two organisms are under discussion.

Throughout the process the silk appears to have a nematic texture,[60] in a manner similar to a liquid crystal, arising in part due to the high protein concentration of silk dope (around 30% in terms of weight per volume).[61] This allows the silk to flow through the duct as a liquid while maintaining molecular order.

As an example of a complex spinning field, the spinneret apparatus of an adult Araneus diadematus (garden cross spider) consists of many glands shown below.[9] A similar gland architecture appears in the black widow spider.[62]

  • 500 pyriform glands for attachment points
  • 4 ampullate glands for the web frame
  • 300 aciniform glands for the outer lining of egg sacs, and for ensnaring prey
  • 4 tubuliform glands for egg sac silk
  • 4 aggregate glands for adhesive functions
  • 2 coronate glands for the thread of adhesion lines

Artificial synthesis

Single strand of artificial spider silk produced under laboratory conditions

To artificially synthesise spider silk into fibres, two broad tasks are required. These are synthesis of the feedstock (the unspun silk dope in spiders), and synthesis of the production conditions (the funnel, valve, tapering duct, and spigot). Few strategies have produced silk that can efficiently be synthesised into fibres.

Feedstock

The molecular structure of unspun silk is both complex and long. Though this endows the fibres with desirable properties, it also complicates replication. Various organisms have been used as a basis for attempts to replicate necessary protein components. These proteins must then be extracted, purified, and then spun before their properties can be tested.

Organism Details Average Maximum breaking stress (MPa) Average Strain (%) Reference
Darwin's bark spider (Caerostris darwini) Malagasy spider famed for making 25 m long strands. "C. darwini silk is more than twice as tough as any previously described silk"[citation needed] 1850 ±350 33 ±0.08 [27]
Nephila clavipes Typical golden orb weaving spider 710–1200 18–27 [63][64]
Bombyx mori Silkworms Silkworms genetically altered to express spider proteins and fibres.[65] 660 18.5 [66]
Escherichia coli Synthesising a large and repetitive molecule (~300 kDa) is complex, but required for the strongest silk. Here E. coli was engineered to produce a 556 kDa protein. Fibers spun from these synthetic spidroins are the first to fully replicate the mechanical performance of natural spider silk by all common metrics. 1030 ±110 18 ±6 [67]
Goats Genetically modified to secrete silk proteins in their milk. 285–250 30–40 [68]
Tobacco & potato plants Genetically modified to produce silk proteins. Patents were granted in 2010,[69] but no fibres have yet been described. n/a n/a [70]

Geometry

Spider silks with comparatively simple molecular structure need complex ducts to be able to form an effective fibre. Approaches:

Syringe and needle

Feedstock is forced through a hollow needle using a syringe.[71][72]

Although cheap and easy to produce, gland shape and conditions are loosely approximated. Fibres created using this method may need encouragement to solidify by removing water from the fibre with chemicals such as (environmentally undesirable) methanol[73] or acetone,[72] and also may require later stretching of the fibre to achieve desirable properties.[74][71]

Superhydrophobic surfaces

Placing a solution of spider silk on a superhydrophobic surface can generate sheets, particles, and nanowires of spider silk.[75][76]

Sheets

Self-assembly of silk at standing liquid-gas interphases of a solution tough and strong sheets. These sheets are now explored for mimicking the basal membrane in tissue modeling.[77][78]

Microfluidics

Microfluidics have the advantage of being controllable and able to test spin small volumes of unspun fibre,[79][80] but setup and development costs are high. A patent has been granted and continuously spun fibres have achieved commercial use.[81]

Electrospinning

Electrospinning is an old technique whereby a fluid is held in a container such that it flows out through capillary action. A conducting substrate is positioned below, and a difference in electrical potential is applied between the fluid and the substrate. The fluid is attracted to the substrate, and tiny fibres jump from their point of emission, the Taylor cone, to the substrate, drying as they travel. This method creates nano-scale fibres from silk dissected from organisms and regenerated silk fibroin.[citation needed]

Other shapes

Silk can be formed into other shapes and sizes such as spherical capsules for drug delivery, cell scaffolds and wound healing, textiles, cosmetics, coatings, and many others.[82][83] Spider silk proteins can self-assemble on superhydrophobic surfaces into nanowires, as well as micron-sized circular sheets.[83] Recombinant spider silk proteins can self-assemble at the liquid-air interface of a standing solution to form protein-permeable, strong and flexible nanomembranes that support cell proliferation. Potential applications include skin transplants, and supportive membranes in organ-on-a-chip.[84] These nanomembranes have been used to create a static in-vitro model of a blood vessel.[85]

Synthetic spider silk

Proposed framework for producing artificial skin from spider silk to help patients with burns.

Replicating the complex conditions required to produce comparable fibres has challenged research and early-stage manufacturing. Through genetic engineering, E. coli bacteria, yeasts, plants, silkworms, and animals other than silkworms have been used to produce spider silk-like proteins, which have different characteristics than those from a spider.[86] Extrusion of protein fibres in an aqueous environment is known as "wet-spinning". This process has produced silk fibres of diameters ranging from 10 to 60 μm, compared to diameters of 2.5–4 μm for natural spider silk. Artificial spider silks have fewer and simpler proteins than natural dragline silk, and consequently offer half the diameter, strength, and flexibility of natural dragline silk.[86]

Research

  • In March 2010, researchers from the Korea Advanced Institute of Science & Technology succeeded in making spider silk directly using E. coli modified with certain genes of the spider Nephila clavipes. This approach eliminates the need to "milk" spiders.[87]
  • A 556 kDa spider silk protein was manufactured from 192 repeat motifs of the N. clavipes dragline spidroin, having similar mechanical characteristics as their natural counterparts, i.e., tensile strength (1.03 ± 0.11 GPa), modulus (13.7 ± 3.0 GPa), extensibility (18 ± 6%), and toughness (114 ± 51 MJ/m3).[67]
  • AMSilk developed spidroin using bacteria.[86][88]
  • Bolt Threads produced a recombinant spidroin using yeast, for use in apparel fibers and personal care. They produced the first commercial apparel products made of recombinant spider silk, trademarked Microsilk, demonstrated in ties and beanies.[89][90]
  • Kraig Biocraft Laboratories used research from the Universities of Wyoming and Notre Dame to create silkworms genetically altered to produce spider silk.[91][92]
  • Defunct Canadian biotechnology company Nexia produced spider silk protein in transgenic goats; the milk produced by the goats contained significant quantities of the protein, 1–2 grams of silk proteins per litre of milk. Attempts to spin the protein into a fibre similar to natural spider silk resulted in fibres with tenacities of 2–3 grams per denier.[93] Nexia used wet spinning and squeezed the silk protein solution through small extrusion holes to simulate the spinneret, but this was not sufficient to replicate native spider silk properties.[94]
  • Spiber produced a synthetic spider silk (Q/QMONOS). In partnership with Goldwin, a ski parka made from this was in testing in 2016.[95][96]

Research

Significant papers (50 or more citations)
Area of contribution Year Main researchers Title Contribution to the field
Chemical Basis 1960 Fischer, F. & Brander, J.[97] "Eine Analyse der Gespinste der Kreuzspinne" (Amino acid composition analysis of spider silk)
1960 Lucas, F. et al.[98][99] "The Composition of Arthropod Silk Fibroins; Comparative studies of fibroins"
Gene Sequence 1990 Xu, M. & Lewis, R. V.[100] "Structure of a Protein Superfiber − Spider Dragline Silk"
Mechanical Properties 1964 Lucas, F.[101] "Spiders and their silks" First time mechanical properties of spider silk compared with other materials in a scientific paper.
1989 Vollrath, F. & Edmonds, D. T.[102] "Modulation of the Mechanical Properties of Spider Silk by Coating with Water" First important paper suggesting the water interplay with spider silk fibroin modulating silk properties.
2001 Vollrath, F. & Shao, Z.Z.[103] "The effect of spinning conditions on the mechanics of a spider's dragline silk"
2006 Plaza, G.R., Guinea, G.V., Pérez-Rigueiro, J. & Elices, M.[17] "Thermo-hygro-mechanical behavior of spider dragline silk: Glassy and rubbery states" Combined effect of humidity and temperature on mechanical properties. Glass-transition temperature dependence on humidity.
Structural Characterisation 1992 Hinman, M.B. & Lewis, R. V[4] "Isolation of a clone encoding a second dragline silk fibroin. Nephila clavipes dragline silk is a two-protein fiber"
1994 Simmons, A. et al.[104] "Solid-State C-13 Nmr of Nephila-Clavipes Dragline Silk Establishes Structure and Identity of Crystalline Regions" First NMR study of spider silk.
1999 Shao, Z., Vollrath, F. et al.[105] "Analysis of spider silk in native and supercontracted states using Raman spectroscopy" First Raman study of spider silk.
1999 Riekel, C., Muller, M.et al.[106] "Aspects of X-ray diffraction on single spider fibers" First X-ray on single spider silk fibres.
2000 Knight, D.P., Vollrath, F. et al.[107] "Beta transition and stress-induced phase separation in the spinning of spider dragline silk" Secondary structural transition confirmation during spinning.
2001 Riekel, C. & Vollrath, F.[108] "Spider silk fibre extrusion: combined wide- and small-angle X- ray microdiffraction experiments" First X-ray on spider silk dope.
2002 Van Beek, J. D. et al.[6] "The molecular structure of spider dragline silk: Folding and orientation of the protein backbone"
Structure-Property Relationship
1994 Termonia, Y[10] "Molecular Modeling of Spider Silk Elasticity" X-ray evidence presented in this paper; simple model of crystallites embedded in amorphous regions.
1996 Simmons, A. et al.[5] "Molecular orientation and two-component nature of the crystalline fraction of spider dragline silk" Two types of alanine-rich crystalline regions were defined.
2006 Vollrath, F. & Porter, D.[109] "Spider silk as an archetypal protein elastomer" New insight and model to spider silk based on Group Interaction Modelling.
Native Spinning 1991 Kerkam, K., Kaplan, D. et al.[110] "Liquid Crystallinity of Natural Silk Secretions"
1999 Knight, D.P. & Vollrath, F.[111] "Liquid crystals and flow elongation in a spider's silk production line"
2001 Vollrath, F. & Knight, D.P.[23] "Liquid crystalline spinning of spider silk" Most cited spider silk paper
2005 Guinea, G.V., Elices, M., Pérez-Rigueiro, J. & Plaza, G.R.[16] "Stretching of supercontracted fibers: a link between spinning and the variability of spider silk" Explanation of the variability of mechanical properties.
Reconstituted /Synthetic Spider Silk and Artificial Spinning
1998 Arcidiacono, S., Kaplan, D.L. et al.[112] "Purification and characterization of recombinant spider silk expressed in Escherichia coli"
1998 Seidel, A., Jelinski, L.W. et al.[113] "Artificial Spinning of Spider Silk" First controlled wet-spinning of reconstituted spider silk.

Human uses

A cape made from Madagascar golden orb spider silk[114]

The earliest recorded attempt to weave fabric from spider silk was in 1709 by François Xavier Bon who, using a process similar to creating silkworm silk, wove silk derived spider's egg cocoons into stockings and gloves. Fifty years later Jesuit missionary Ramón M. Termeyer (pl), invented a reeling device for harvesting spider silk directly from spiders, allowing it to be spun into threads. Neither Bon nor Termeyer were successful in producing commercially viable quantities.[115]

The development of methods to mass-produce spider silk led to the manufacturing of military, medical, and consumer goods, such as ballistic armour, athletic footwear, personal care products, breast implant and catheter coatings, mechanical insulin pumps, fashion clothing, and outerwear.[86] However, due to the difficulties in extracting and processing, the largest known piece of cloth made of spider silk is an 11-by-4-foot (3.4 by 1.2 m) textile with a golden tint made in Madagascar in 2009.[116] Eighty-two people worked for four years to collect over one million golden orb spiders and extract silk from them.[117] In 2012, spider silk fibres were used to create a set of violin strings.[118]

Medicine

Peasants in the southern Carpathian Mountains used to cut up tubes built by Atypus and cover wounds with the inner lining. It reportedly facilitated healing, and connected with the skin. This is believed to be due to the silk's antiseptic properties,[119] and because silk is rich in vitamin K, which can aid in clotting blood.[120][verify] N. clavipes silk was used in research concerning mammalian neuronal regeneration.[121]

Scientific instruments

Spider silk has been used as a thread for crosshairs in optical instruments such as telescopes, microscopes,[122] and telescopic rifle sights.[123] In 2011, silk fibres were used to generate fine diffraction patterns over N-slit interferometric signals used in optical communications.[124] Silk has been used to create biolenses that could be used in conjunction with lasers to create high-resolution images of the inside of the human body.[125]

Silk has been used to suspend inertial confinement fusion targets during laser ignition, as it remains considerably elastic and has a high energy to break at temperatures as low as 10–20 K. In addition, it is made from "light" atomic number elements that emit no x-rays during irradiation that could preheat the target, limiting the pressure differential required for fusion.[126]

References

  1. 1.0 1.1 Miyashita, Tadashi; Maezono, Yasunori; Shimazaki, Aya (2004). "Silk feeding as an alternative foraging tactic in a kleptoparasitic spider under seasonally changing environments". Journal of Zoology 262 (3): 225–29. doi:10.1017/S0952836903004540. http://frank.itlab.us/photo_essays/papers/Argyrodes_kleptoparasite_spider.pdf. 
  2. Work, Robert W.; Emerson, Paul D. (1982). "An Apparatus and Technique for the Forcible Silking of Spiders". Journal of Arachnology 10 (1): 1–10. 
  3. Scott, Catherine E.; Anderson, Alissa G.; Andrade, Maydianne C. B. (August 2018). "A review of the mechanisms and functional roles of male silk use in spider courtship and mating". The Journal of Arachnology 46 (2): 173–206. doi:10.1636/JoA-S-17-093.1. ISSN 0161-8202. https://bioone.org/journals/the-journal-of-arachnology/volume-46/issue-2/JoA-S-17-093.1/A-review-of-the-mechanisms-and-functional-roles-of-male/10.1636/JoA-S-17-093.1.full. 
  4. 4.0 4.1 Hinman, M. B.; Lewis, R. V. (1992). "Isolation of a clone encoding a second dragline silk fibroin. Nephila clavipes dragline silk is a two-protein fiber". J. Biol. Chem. 267 (27): 19320–24. doi:10.1016/S0021-9258(18)41777-2. PMID 1527052. 
  5. 5.0 5.1 5.2 5.3 Simmons, A. H.; Michal, C. A.; Jelinski, L. W. (1996). "Molecular orientation and two-component nature of the crystalline fraction of spider dragline silk". Science 271 (5245): 84–87. doi:10.1126/science.271.5245.84. PMID 8539605. Bibcode1996Sci...271...84S. 
  6. 6.0 6.1 van Beek, J. D.; Hess, S.; Vollrath, F.; Meier, B. H. (2002). "The molecular structure of spider dragline silk: Folding and orientation of the protein backbone". Proc. Natl. Acad. Sci. U.S.A. 99 (16): 10266–71. doi:10.1073/pnas.152162299. PMID 12149440. Bibcode2002PNAS...9910266V. 
  7. Liu, Y.; Sponner, A.; Porter, D.; Vollrath, F. (2008). "Proline and Processing of Spider Silks". Biomacromolecules 9 (1): 116–21. doi:10.1021/bm700877g. PMID 18052126. 
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