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- PDB-7jti: Interphotoreceptor retinoid-binding protein (IRBP) in complex wit... -
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Open data
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Basic information
Entry | Database: PDB / ID: 7jti | |||||||||||||||
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Title | Interphotoreceptor retinoid-binding protein (IRBP) in complex with a monoclonal antibody (F3F5 mAb5) | |||||||||||||||
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![]() | TRANSPORT PROTEIN/IMMUNE SYSTEM / IRBP / ![]() ![]() | |||||||||||||||
Function / homology | ![]() cone matrix sheath / The retinoid cycle in cones (daylight vision) / The canonical retinoid cycle in rods (twilight vision) / all-trans-retinol binding / ![]() ![]() ![]() ![]() Similarity search - Function | |||||||||||||||
Biological species | ![]() ![]() ![]() ![]() ![]() ![]() | |||||||||||||||
Method | ![]() ![]() ![]() | |||||||||||||||
![]() | Sears, A.E. / Albiez, S. / Gulati, S. / Wang, B. / Kiser, P. / Kovacik, L. / Engel, A. / Stahlberg, H. / Palczewski, K. | |||||||||||||||
Funding support | ![]() ![]()
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![]() | ![]() Title: Single particle cryo-EM of the complex between interphotoreceptor retinoid-binding protein and a monoclonal antibody. Authors: Avery E Sears / Stefan Albiez / Sahil Gulati / Benlian Wang / Philip Kiser / Lubomir Kovacik / Andreas Engel / Henning Stahlberg / Krzysztof Palczewski / ![]() ![]() Abstract: Interphotoreceptor retinoid-binding protein (IRBP) is a highly expressed protein secreted by rod and cone photoreceptors that has major roles in photoreceptor homeostasis as well as retinoid and ...Interphotoreceptor retinoid-binding protein (IRBP) is a highly expressed protein secreted by rod and cone photoreceptors that has major roles in photoreceptor homeostasis as well as retinoid and polyunsaturated fatty acid transport between the neural retina and retinal pigment epithelium. Despite two crystal structures reported on fragments of IRBP and decades of research, the overall structure of IRBP and function within the visual cycle remain unsolved. Here, we studied the structure of native bovine IRBP in complex with a monoclonal antibody (mAb5) by cryo-electron microscopy, revealing the tertiary and quaternary structure at sufficient resolution to clearly identify the complex components. Complementary mass spectrometry experiments revealed the structure and locations of N-linked carbohydrate post-translational modifications. This work provides insight into the structure of IRBP, displaying an elongated, flexible three-dimensional architecture not seen among other retinoid-binding proteins. This work is the first step in elucidation of the function of this enigmatic protein. | |||||||||||||||
History |
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Structure visualization
Movie |
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Structure viewer | Molecule: ![]() ![]() |
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Downloads & links
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Download
PDBx/mmCIF format | ![]() | 294.3 KB | Display | ![]() |
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PDB format | ![]() | 240.6 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Arichive directory | ![]() ![]() | HTTPS FTP |
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-Related structure data
Related structure data | ![]() 22474MC M: map data used to model this data C: citing same article ( |
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Similar structure data | |
EM raw data | ![]() Data size: 729.9 Data #1: Unaligned multi-frame micrographs of IRBP and antibody [micrographs - multiframe]) |
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Links
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Assembly
Deposited unit | ![]()
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Components
-Retinol-binding protein ... , 4 types, 4 molecules ABCD
#3: Protein | Mass: 33267.301 Da / Num. of mol.: 1 / Fragment: Module 1 (UNP residues 329-631) / Source method: isolated from a natural source / Source: (natural) ![]() ![]() ![]() ![]() |
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#4: Protein | Mass: 33386.637 Da / Num. of mol.: 1 / Fragment: Module 2 / Source method: isolated from a natural source / Source: (natural) ![]() ![]() ![]() |
#5: Protein | Mass: 32399.768 Da / Num. of mol.: 1 / Fragment: Module 3 (UNP residues 633-932) / Source method: isolated from a natural source / Source: (natural) ![]() ![]() ![]() |
#6: Protein | Mass: 32192.508 Da / Num. of mol.: 1 / Fragment: Module 4 (UNP residues 936-1231) / Source method: isolated from a natural source / Source: (natural) ![]() ![]() ![]() |
-Antibody , 2 types, 2 molecules LH
#1: Antibody | Mass: 22596.021 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() ![]() ![]() ![]() ![]() |
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#2: Antibody | Mass: 23777.783 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() ![]() ![]() ![]() ![]() |
-Experimental details
-Experiment
Experiment | Method: ![]() |
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EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: ![]() |
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Sample preparation
Component |
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Molecular weight | Value: 0.193 MDa / Experimental value: YES | |||||||||||||||||||||||||
Source (natural) |
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Source (recombinant) | Organism: ![]() ![]() ![]() | |||||||||||||||||||||||||
Buffer solution | pH: 8 | |||||||||||||||||||||||||
Buffer component |
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Specimen | Conc.: 0.2 mg/ml / Embedding applied: NO / Shadowing applied: NO / Staining applied![]() ![]() Details: The sample had minor aggregation but was overall monodisperse. | |||||||||||||||||||||||||
Specimen support | Grid material: COPPER / Grid mesh size: 400 divisions/in. / Grid type: Quantifoil R1.2/1.3 | |||||||||||||||||||||||||
Vitrification![]() | Instrument: FEI VITROBOT MARK IV / Cryogen name: ETHANE / Humidity: 90 % / Chamber temperature: 277 K / Details: Blot for 3 seconds before plunging. |
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Electron microscopy imaging
Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Microscopy | Model: FEI TITAN KRIOS |
Electron gun | Electron source![]() ![]() |
Electron lens | Mode: BRIGHT FIELD![]() |
Specimen holder | Cryogen: NITROGEN Specimen holder model: GATAN 910 MULTI-SPECIMEN SINGLE TILT CRYO TRANSFER HOLDER |
Image recording | Average exposure time: 1 sec. / Electron dose: 80 e/Å2 / Detector mode: SUPER-RESOLUTION / Film or detector model: GATAN K2 QUANTUM (4k x 4k) / Num. of grids imaged: 4 / Num. of real images: 2649 Details: Images were collected in movie mode at 35 frames per second. |
EM imaging optics | Energyfilter name![]() |
Image scans | Width: 1000 / Height: 1000 / Movie frames/image: 35 |
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Processing
EM software |
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Image processing | Details: The selected images were low-pass filtered and normalized. | ||||||||||||||||||||||||||||||||
CTF correction![]() | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||||||||||
Particle selection | Num. of particles selected: 281804 Details: Ab initio, cisTEM processing using low-pass filtered reconstruction | ||||||||||||||||||||||||||||||||
3D reconstruction![]() | Resolution: 7.4 Å / Resolution method: FSC 0.5 CUT-OFF / Num. of particles: 17900 / Symmetry type: POINT | ||||||||||||||||||||||||||||||||
Atomic model building | B value: 156 / Protocol: RIGID BODY FIT / Space: REAL / Target criteria: Correlation coefficient | ||||||||||||||||||||||||||||||||
Atomic model building | PDB-ID: 1J7X Pdb chain-ID: A |