Difference between revisions of "Part:BBa K4247002"

 
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===Minispidroin_CT===
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This part codes for the C-terminal domain of minispidroin, a highly soluble spider silk protein. This part, together with BBa_K4247000 and BBa_K4247001 gives the full sequence of the minispidroin protein. 
  
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==Usage and Biology==
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Dragline silk produced by spiders is one of the strongest natural materials to exist and it is mainly made up of structural proteins called spidroins. These spidroins consist of non-repetitive N-terminal and C-terminal domains and a repetitive central part consisting of tandem repeats of a certain amino acid sequence. These sequences are rich in alanine and glycine to form the crystalline and amorphous parts of the fibre respectively.
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There are many research articles whose authors could successfully produce recombinant spider silk proteins and spin them into fibres by mimicking the conditions of the spider’s silk gland where the fibers are formed naturally. But a major drawback in many of these recombinant spidroins was their low solubility. It has been found that the N-terminus of the spidroin is highly soluble at neutral pH which contributes to the solubility of the protein.
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In the spider's silk gland, before spinning, the spidroins remain in a highly concentrated and soluble state. Then, this highly concentrated spidroin solution called spinning dope is subject to a gradual drop in pH form 7.6 to 5.7 along the gland which triggers the formation of the fiber. This drop in pH triggers the N-terminus to be more stable and form large network-like structures whereas the C-terminus becomes more unstable to drive spontaneous fibre formation by forming the beta-sheet fibrils which form the core of the fiber.
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This clearly shows us that the solubility and pH sensitivity have a huge effect on the N- and C-terminus of the spidroin which thus affects the formation of fibers. It has been found that the N-terminus of MaSp1 (Major ampullate spidroin 1) from Euprosthenops australis, shows extremely high solubility and pH sensitivity whereas the C-terminus has low solubility and is inert to pH changes and vice versa for the MiSp (Minor ampullate spidroin) of Araneus ventricosus.
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So, minispidroin, a recombinant protein was produced by combining the N-terminal of E.australis Masp1, C-terminal of A.ventricosus Misp and the repetitive part of E.australis Masp. This chimeric protein has been designed for optimal spinning since it has high solubility and high sensitivity to pH changes which are 2 factors that are crucial for spinning.
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Herein, part BBa_K4247002 contains the coding sequence for the C-terminus of the minispidroin protein.

Revision as of 10:19, 23 September 2022

Minispidroin_CT

This part codes for the C-terminal domain of minispidroin, a highly soluble spider silk protein. This part, together with BBa_K4247000 and BBa_K4247001 gives the full sequence of the minispidroin protein.

Usage and Biology

Dragline silk produced by spiders is one of the strongest natural materials to exist and it is mainly made up of structural proteins called spidroins. These spidroins consist of non-repetitive N-terminal and C-terminal domains and a repetitive central part consisting of tandem repeats of a certain amino acid sequence. These sequences are rich in alanine and glycine to form the crystalline and amorphous parts of the fibre respectively.

There are many research articles whose authors could successfully produce recombinant spider silk proteins and spin them into fibres by mimicking the conditions of the spider’s silk gland where the fibers are formed naturally. But a major drawback in many of these recombinant spidroins was their low solubility. It has been found that the N-terminus of the spidroin is highly soluble at neutral pH which contributes to the solubility of the protein.

In the spider's silk gland, before spinning, the spidroins remain in a highly concentrated and soluble state. Then, this highly concentrated spidroin solution called spinning dope is subject to a gradual drop in pH form 7.6 to 5.7 along the gland which triggers the formation of the fiber. This drop in pH triggers the N-terminus to be more stable and form large network-like structures whereas the C-terminus becomes more unstable to drive spontaneous fibre formation by forming the beta-sheet fibrils which form the core of the fiber.

This clearly shows us that the solubility and pH sensitivity have a huge effect on the N- and C-terminus of the spidroin which thus affects the formation of fibers. It has been found that the N-terminus of MaSp1 (Major ampullate spidroin 1) from Euprosthenops australis, shows extremely high solubility and pH sensitivity whereas the C-terminus has low solubility and is inert to pH changes and vice versa for the MiSp (Minor ampullate spidroin) of Araneus ventricosus.

So, minispidroin, a recombinant protein was produced by combining the N-terminal of E.australis Masp1, C-terminal of A.ventricosus Misp and the repetitive part of E.australis Masp. This chimeric protein has been designed for optimal spinning since it has high solubility and high sensitivity to pH changes which are 2 factors that are crucial for spinning.

Herein, part BBa_K4247002 contains the coding sequence for the C-terminus of the minispidroin protein.