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- SASDCX7: TET12(1.10)S-f5b -

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Basic information

Entry
Database: SASBDB / ID: SASDCX7
SampleTET12(1.10)S-f5b
  • TET12(1.10)S-f5b (protein), synthetic construct
Biological speciessynthetic construct (others)
CitationJournal: Nat Biotechnol / Year: 2017
Title: Design of coiled-coil protein-origami cages that self-assemble in vitro and in vivo.
Authors: Ajasja Ljubetič / Fabio Lapenta / Helena Gradišar / Igor Drobnak / Jana Aupič / Žiga Strmšek / Duško Lainšček / Iva Hafner-Bratkovič / Andreja Majerle / Nuša Krivec / Mojca ...Authors: Ajasja Ljubetič / Fabio Lapenta / Helena Gradišar / Igor Drobnak / Jana Aupič / Žiga Strmšek / Duško Lainšček / Iva Hafner-Bratkovič / Andreja Majerle / Nuša Krivec / Mojca Benčina / Tomaž Pisanski / Tanja Ćirković Veličković / Adam Round / José María Carazo / Roberto Melero / Roman Jerala /
Abstract: Polypeptides and polynucleotides are natural programmable biopolymers that can self-assemble into complex tertiary structures. We describe a system analogous to designed DNA nanostructures in which ...Polypeptides and polynucleotides are natural programmable biopolymers that can self-assemble into complex tertiary structures. We describe a system analogous to designed DNA nanostructures in which protein coiled-coil (CC) dimers serve as building blocks for modular de novo design of polyhedral protein cages that efficiently self-assemble in vitro and in vivo. We produced and characterized >20 single-chain protein cages in three shapes-tetrahedron, four-sided pyramid, and triangular prism-with the largest containing >700 amino-acid residues and measuring 11 nm in diameter. Their stability and folding kinetics were similar to those of natural proteins. Solution small-angle X-ray scattering (SAXS), electron microscopy (EM), and biophysical analysis confirmed agreement of the expressed structures with the designs. We also demonstrated self-assembly of a tetrahedral structure in bacteria, mammalian cells, and mice without evidence of inflammation. A semi-automated computational design platform and a toolbox of CC building modules are provided to enable the design of protein cages in any polyhedral shape.
Contact author
  • Jana Aupic (National Institute of Chemistry, Slovenia)

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

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Models

Model #1588
Type: atomic / Software: (9.16) / Radius of dummy atoms: 1.90 A
Search similar-shape structures of this assembly by Omokage search (details)

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Sample

SampleName: TET12(1.10)S-f5b / Specimen concentration: 1.00-7.00
BufferName: 20 mM Tris 150 mM NaCl 10% glycerol / pH: 7.5
Entity #811Type: protein / Description: TET12(1.10)S-f5b / Formula weight: 53.191 / Num. of mol.: 1 / Source: synthetic construct
Sequence: MLEEELKQLE EELQAIEEQL AQLQWKAQAR KEKLAQLKEK LSGPGSPEDE NSQLEEKISQ LKQKNSQLKE EIQQLEYGSG PGDIEQELER AKQSIRRLEQ EVNQERSRMQ YLQTLLSKSG PGQLEDKVEE LLSKNYHLEN EVSRLKKLVG SGPGLEEELK QLEEELQAIE ...Sequence:
MLEEELKQLE EELQAIEEQL AQLQWKAQAR KEKLAQLKEK LSGPGSPEDE NSQLEEKISQ LKQKNSQLKE EIQQLEYGSG PGDIEQELER AKQSIRRLEQ EVNQERSRMQ YLQTLLSKSG PGQLEDKVEE LLSKNYHLEN EVSRLKKLVG SGPGLEEELK QLEEELQAIE EQLAQLQWKA QARKEKLAQL KEKLSGPGSP EDEIQSLEEK NSQLKQEISQ LEEKNQQLKY GSGPGQLEDK VEELLSKNYH LENEVSRLKK LVGSGPGSPE DKNSQLKEEI QQLEEENQQL EEKISQLKYG SGPGSPEDEI QQLEEEISQL EQKNSQLKEK NQQLKYGSGP GSPEDKISQL KEENQQLEQK IQQLKEENSQ LEYGSGPGDI EQELERAKQS IRRLEQEVNQ ERSRMQYLQT LLSKSGPGSP EDKISQLKQK IQQLKQENQQ LEEENSQLEY GLEHHHHHHH H

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Experimental information

BeamInstrument name: ESRF BM29 / City: Grenoble / : France / Type of source: X-ray synchrotronSynchrotron / Wavelength: 0.1 Å / Dist. spec. to detc.: 2.89 mm
DetectorName: Pilatus 1M
Scan
Title: TET12(1.10)S-f5b / Measurement date: Apr 7, 2016 / Storage temperature: 20 °C / Cell temperature: 20 °C / Exposure time: 2 sec. / Number of frames: 10 / Unit: 1/nm /
MinMax
Q0.1694 4.946
Distance distribution function P(R)
Sofotware P(R): GNOM 5.0 / Number of points: 471 /
MinMax
Q0.197645 2.41386
P(R) point1 471
R0 11.18
Result
Type of curve: single_conc
ExperimentalStandardStandard errorPorod
MW47.2 kDa47.2 kDa0.2 75 kDa
Volume---127 nm3

P(R)P(R) errorGuinierGuinier error
Forward scattering, I0312.1 0.3 312.65 1
Radius of gyration, Rg3.375 nm0.004 3.38 nm0.02

MinMaxError
D-11.18 1
Guinier point7 46 -

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