Difference between revisions of "Part:BBa K2686006"
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This Composite part consists of an encapsulin protein with a HexaHistidine linker and an OT1 peptide fused to the C terminus, followed by a T7 RBS and a sfGFP protein with a 15 amino acid long peptide tag. This peptide tag allows the sfGFP to bind to the encapsulin's interior surface, thus allowing the loading of sfGFP in the Encapsulin multimer. This would allow having a fluorescent Encapsulin protein. | This Composite part consists of an encapsulin protein with a HexaHistidine linker and an OT1 peptide fused to the C terminus, followed by a T7 RBS and a sfGFP protein with a 15 amino acid long peptide tag. This peptide tag allows the sfGFP to bind to the encapsulin's interior surface, thus allowing the loading of sfGFP in the Encapsulin multimer. This would allow having a fluorescent Encapsulin protein. | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
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===Assembly=== | ===Assembly=== | ||
The self assembly of the encapsulin 60-mer was first examined using SDS PAGE, where a band around 30.71kDa band is expected to form. Additionally due to Encapsulin's exceptional heat stability the 1.98MDa complex also appears on the gel after SDS denaturation. | The self assembly of the encapsulin 60-mer was first examined using SDS PAGE, where a band around 30.71kDa band is expected to form. Additionally due to Encapsulin's exceptional heat stability the 1.98MDa complex also appears on the gel after SDS denaturation. | ||
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[[File:NativeGel.png|thumb|center|upright=3|Native PAGE gel of sfGFP, HexaHistidine-OT1 Encapsulin and HexaHistidine-OT1 Encapsulin sfGFP-tag. On the '''left''' is the fluorescent image of the gel and o the '''right''' is the gel after Coomassie staining. '''Before''' ('''B''') heat purification procedure outlined in '''Purification''' section, '''Supernatant''' ('''S''') after the heat purification procedure. '''Stars''' <nowiki>★</nowiki> show the bands for monomers of HexaHistidine-OT1 Encapsulin (<bbpart>BBa_K2686000</bbpart>,<bbpart>BBa_K2686006</bbpart>) with sfGFP-tag bound to them, increasing the molecular weight of the complex when compared to sfGFP alone. '''Triangles''' <nowiki>▲</nowiki> signify a 60-mer band to the right. | [[File:NativeGel.png|thumb|center|upright=3|Native PAGE gel of sfGFP, HexaHistidine-OT1 Encapsulin and HexaHistidine-OT1 Encapsulin sfGFP-tag. On the '''left''' is the fluorescent image of the gel and o the '''right''' is the gel after Coomassie staining. '''Before''' ('''B''') heat purification procedure outlined in '''Purification''' section, '''Supernatant''' ('''S''') after the heat purification procedure. '''Stars''' <nowiki>★</nowiki> show the bands for monomers of HexaHistidine-OT1 Encapsulin (<bbpart>BBa_K2686000</bbpart>,<bbpart>BBa_K2686006</bbpart>) with sfGFP-tag bound to them, increasing the molecular weight of the complex when compared to sfGFP alone. '''Triangles''' <nowiki>▲</nowiki> signify a 60-mer band to the right. | ||
From left to right: '''(1-2)''' Negative control (cell-free TX-TL expression without DNA), '''(2-4)''' HexaHistidine-OT1 Encapsulin (<bbpart>BBa_K2686000</bbpart>), showing no fluorescence on the left gel, has a band for 60-mer on stained gel (<nowiki>▲</nowiki>). '''(5-6)''' sfGFP protein, the fluorescent bands can be easily seen as large smears on the left. '''(7-8)''' HexaHistidine-OT1 Encapsulin and sfGFP-tag (<bbpart>BBa_K2686006</bbpart>) shown by a <nowiki>★</nowiki>. The difference in height between the bands of sfGFP compared to the <nowiki>★</nowiki> is striking and suggests that the sfGFP-tag binds to the HexaHistidine-OT1 Encapsulin monomers. In addition there seems to be a small amount of 60-mer indicated by <nowiki>▲</nowiki>. '''(9-10)''' Encapsulin (<bbpart>BBa_K2686001</bbpart>) does assemble to form the 60-mer <nowiki>▲</nowiki> as seen on the stained gel. '''(11)''' HexaHistidine-OT1 Encapsulin and sfGFP-tag (<bbpart>BBa_K2686006</bbpart>), on the left the presumed <nowiki>★</nowiki> protein dimer is seen to be higher than the sfGFP in lane '''12''', no particular bands can be identified on the right. '''(12)''' sfGFP, fluorescent band is seen to be lower than for lane '''11'''. | From left to right: '''(1-2)''' Negative control (cell-free TX-TL expression without DNA), '''(2-4)''' HexaHistidine-OT1 Encapsulin (<bbpart>BBa_K2686000</bbpart>), showing no fluorescence on the left gel, has a band for 60-mer on stained gel (<nowiki>▲</nowiki>). '''(5-6)''' sfGFP protein, the fluorescent bands can be easily seen as large smears on the left. '''(7-8)''' HexaHistidine-OT1 Encapsulin and sfGFP-tag (<bbpart>BBa_K2686006</bbpart>) shown by a <nowiki>★</nowiki>. The difference in height between the bands of sfGFP compared to the <nowiki>★</nowiki> is striking and suggests that the sfGFP-tag binds to the HexaHistidine-OT1 Encapsulin monomers. In addition there seems to be a small amount of 60-mer indicated by <nowiki>▲</nowiki>. '''(9-10)''' Encapsulin (<bbpart>BBa_K2686001</bbpart>) does assemble to form the 60-mer <nowiki>▲</nowiki> as seen on the stained gel. '''(11)''' HexaHistidine-OT1 Encapsulin and sfGFP-tag (<bbpart>BBa_K2686006</bbpart>), on the left the presumed <nowiki>★</nowiki> protein dimer is seen to be higher than the sfGFP in lane '''12''', no particular bands can be identified on the right. '''(12)''' sfGFP, fluorescent band is seen to be lower than for lane '''11'''. |
Revision as of 11:18, 17 October 2018
Encapsulin protein with HexaHistidine insert, OT1 peptide at C terminus and a sfGFP-tag protein.
This Composite part consists of an encapsulin protein with a HexaHistidine linker and an OT1 peptide fused to the C terminus, followed by a T7 RBS and a sfGFP protein with a 15 amino acid long peptide tag. This peptide tag allows the sfGFP to bind to the encapsulin's interior surface, thus allowing the loading of sfGFP in the Encapsulin multimer. This would allow having a fluorescent Encapsulin protein.
Usage and Biology
Purification
After having tested a variety of purification procedures, heat purification at 70C for 20 minutes followed by cooling on ice for 15 minutes and a subsequent centrifugation at 12000g for 10 minutes was found to be the most efficient way of isolating the encapsulin (encapsulin ends up in supernatant).
Assembly
The self assembly of the encapsulin 60-mer was first examined using SDS PAGE, where a band around 30.71kDa band is expected to form. Additionally due to Encapsulin's exceptional heat stability the 1.98MDa complex also appears on the gel after SDS denaturation.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 902
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 77
Illegal BglII site found at 492 - 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 902
- 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 902
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 426
Illegal SapI.rc site found at 457
Illegal SapI.rc site found at 955