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- EMDB-44277: Fab1-7 in complex with the capsid of Adeno-associated virus type 9 -
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Open data
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Basic information
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Title | Fab1-7 in complex with the capsid of Adeno-associated virus type 9 | |||||||||
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![]() | Adeno-associated virus / AAV / capsid / Fab-complex / antibody / NAb / VIRUS / VIRAL PROTEIN-IMMUNE SYSTEM complex | |||||||||
Function / homology | Phospholipase A2-like domain / Phospholipase A2-like domain / Parvovirus coat protein VP2 / Parvovirus coat protein VP1/VP2 / Parvovirus coat protein VP2 / Capsid/spike protein, ssDNA virus / T=1 icosahedral viral capsid / structural molecule activity / Capsid protein VP1![]() | |||||||||
Biological species | ![]() ![]() ![]() | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 2.54 Å | |||||||||
![]() | Mietzsch M / McKenna R | |||||||||
Funding support | ![]()
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![]() | ![]() Title: Structural characterization of antibody-responses following Zolgensma treatment for AAV capsid engineering to expand patient cohorts. Authors: Mario Mietzsch / Jane Hsi / Austin R Nelson / Neeta Khandekar / Ann-Maree Huang / Nicholas Jc Smith / Jon Zachary / Lindsay Potts / Michelle A Farrar / Paul Chipman / Mohammad Ghanem / Ian E ...Authors: Mario Mietzsch / Jane Hsi / Austin R Nelson / Neeta Khandekar / Ann-Maree Huang / Nicholas Jc Smith / Jon Zachary / Lindsay Potts / Michelle A Farrar / Paul Chipman / Mohammad Ghanem / Ian E Alexander / Grant J Logan / Juha T Huiskonen / Robert McKenna / ![]() ![]() ![]() Abstract: Monoclonal antibodies are useful tools to dissect the neutralizing antibody response against the adeno-associated virus (AAV) capsids that are used as gene therapy delivery vectors. The presence of ...Monoclonal antibodies are useful tools to dissect the neutralizing antibody response against the adeno-associated virus (AAV) capsids that are used as gene therapy delivery vectors. The presence of pre-existing neutralizing antibodies in large portions of the human population poses a significant challenge for AAV-mediated gene therapy, primarily targeting the capsid leading to vector inactivation and loss of treatment efficacy. This study structurally characterizes the interactions of 21 human-derived neutralizing antibodies from three patients treated with the AAV9 vector, Zolgensma®, utilizing high-resolution cryo-electron microscopy. The antibodies bound to the 2-fold depression or the 3-fold protrusions do not conform to the icosahedral symmetry of the capsid, thus requiring localized reconstructions. These complex structures provide unprecedented details of the mAbs binding interfaces, with many antibodies inducing structural perturbations of the capsid upon binding. Key surface capsid amino acid residues were identified facilitating the design of capsid variants with antibody escape phenotypes. These AAV9 capsid variants have the potential to expand the patient cohort to include those that were previously excluded due to their pre-existing neutralizing antibodies against the wtAAV9 capsid, and the possibly of further treatment to those requiring redosing. | |||||||||
History |
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Structure visualization
Supplemental images |
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Downloads & links
-EMDB archive
Map data | ![]() | 27.5 MB | ![]() | |
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Header (meta data) | ![]() ![]() | 20.1 KB 20.1 KB | Display Display | ![]() |
Images | ![]() | 71.6 KB | ||
Filedesc metadata | ![]() | 6.6 KB | ||
Others | ![]() ![]() | 23 MB 23 MB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 9b6tMC ![]() 9b6oC ![]() 9b6pC ![]() 9b6qC ![]() 9b6rC ![]() 9b6sC ![]() 9b7kC ![]() 9b7lC ![]() 9b7mC ![]() 9b7nC ![]() 9b7oC ![]() 9b7pC ![]() 9b7qC ![]() 9b7rC ![]() 9b7sC ![]() 9b7tC ![]() 9b7uC ![]() 9b7vC ![]() 9b7wC ![]() 9b7xC M: atomic model generated by this map C: citing same article ( |
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Similar structure data | Similarity search - Function & homology ![]() |
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Links
EMDB pages | ![]() ![]() |
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Related items in Molecule of the Month |
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Map
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Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 0.724 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: #2
File | emd_44277_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #1
File | emd_44277_half_map_2.map | ||||||||||||
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Density Histograms |
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Sample components
-Entire : Adeno-associated virus
Entire | Name: ![]() ![]() |
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Components |
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-Supramolecule #1: Adeno-associated virus
Supramolecule | Name: Adeno-associated virus / type: virus / ID: 1 / Parent: 0 / Macromolecule list: all / NCBI-ID: 272636 / Sci species name: Adeno-associated virus / Virus type: VIRION / Virus isolate: SEROTYPE / Virus enveloped: No / Virus empty: No |
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Virus shell | Shell ID: 1 / T number (triangulation number): 1 |
-Macromolecule #1: Capsid protein VP1
Macromolecule | Name: Capsid protein VP1 / type: protein_or_peptide / ID: 1 / Number of copies: 6 / Enantiomer: LEVO |
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Source (natural) | Organism: ![]() ![]() |
Molecular weight | Theoretical: 59.873875 KDa |
Recombinant expression | Organism: ![]() |
Sequence | String: MASGGGAPVA DNNEGADGVG SSSGNWHCDS QWLGDRVITT STRTWALPTY NNHLYKQISN STSGGSSNDN AYFGYSTPWG YFDFNRFHC HFSPRDWQRL INNNWGFRPK RLNFKLFNIQ VKEVTDNNGV KTIANNLTST VQVFTDSDYQ LPYVLGSAHE G CLPPFPAD ...String: MASGGGAPVA DNNEGADGVG SSSGNWHCDS QWLGDRVITT STRTWALPTY NNHLYKQISN STSGGSSNDN AYFGYSTPWG YFDFNRFHC HFSPRDWQRL INNNWGFRPK RLNFKLFNIQ VKEVTDNNGV KTIANNLTST VQVFTDSDYQ LPYVLGSAHE G CLPPFPAD VFMIPQYGYL TLNDGSQAVG RSSFYCLEYF PSQMLRTGNN FQFSYEFENV PFHSSYAHSQ SLDRLMNPLI DQ YLYYLSK TINGSGQNQQ TLKFSVAGPS NMAVQGRNYI PGPSYRQQRV STTVTQNNNS EFAWPGASSW ALNGRNSLMN PGP AMASHK EGEDRFFPLS GSLIFGKQGT GRDNVDADKV MITNEEEIKT TNPVATESYG QVATNHQSAQ AQAQTGWVQN QGIL PGMVW QDRDVYLQGP IWAKIPHTDG NFHPSPLMGG FGMKHPPPQI LIKNTPVPAD PPTAFNKDKL NSFITQYSTG QVSVE IEWE LQKENSKRWN PEIQYTSNYY KSNNVEFAVN TEGVYSEPRP IGTRYLTRNL UniProtKB: Capsid protein VP1 |
-Macromolecule #2: Fab1-7 heavy chain
Macromolecule | Name: Fab1-7 heavy chain / type: protein_or_peptide / ID: 2 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: ![]() |
Molecular weight | Theoretical: 13.235849 KDa |
Recombinant expression | Organism: ![]() |
Sequence | String: QVQLQESGPG LVKPSETLSL TCTVSGDSIR SYYWSWIRQP PGKGLEWIGH IYYSGSTNYK PSLKSRATIL VDTSKNQFSL KLRSVTAAD TAVYYCAREM TGVAGRGWDH WGQGTLVTVS S |
-Macromolecule #3: Fab1-7 light chain
Macromolecule | Name: Fab1-7 light chain / type: protein_or_peptide / ID: 3 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: ![]() |
Molecular weight | Theoretical: 11.328345 KDa |
Recombinant expression | Organism: ![]() |
Sequence | String: ALTQPPSASG TPGQRVTISC SGSSSNIGSN TVNWYQQLPG TAPKLLIFIN NQRPSGVPDR FSGSKSGTSA SLAISGLQSE DEADYYCTT WDGSLNGYVF GTRTEVTVL |
-Experimental details
-Structure determination
Method | cryo EM |
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![]() | single particle reconstruction |
Aggregation state | particle |
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Sample preparation
Buffer | pH: 7.4 |
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Vitrification | Cryogen name: ETHANE |
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Electron microscopy
Microscope | TFS KRIOS |
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Image recording | Film or detector model: FEI FALCON IV (4k x 4k) / Average electron dose: 50.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: ![]() |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 2.1 µm / Nominal defocus min: 0.8 µm |
Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |