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9FDG

Solution structure of a de novo designed 12-stranded transmembrane beta-barrel in LDAO micelles.

Summary for 9FDG
Entry DOI10.2210/pdb9fdg/pdb
NMR InformationBMRB: 52384
DescriptorTMB12sol9_3 (1 entity in total)
Functional Keywordsstructure from cyana 3.98.15, membrane protein
Biological sourcesynthetic construct
Total number of polymer chains1
Total formula weight20349.34
Authors
Muentener, T.,Hiller, S. (deposition date: 2024-05-17, release date: 2024-10-16)
Primary citationBerhanu, S.,Majumder, S.,Muentener, T.,Whitehouse, J.,Berner, C.,Bera, A.K.,Kang, A.,Liang, B.,Khan, N.,Sankaran, B.,Tamm, L.K.,Brockwell, D.J.,Hiller, S.,Radford, S.E.,Baker, D.,Vorobieva, A.A.
Sculpting conducting nanopore size and shape through de novo protein design.
Science, 385:282-288, 2024
Cited by
PubMed Abstract: Transmembrane β-barrels have considerable potential for a broad range of sensing applications. Current engineering approaches for nanopore sensors are limited to naturally occurring channels, which provide suboptimal starting points. By contrast, de novo protein design can in principle create an unlimited number of new nanopores with any desired properties. Here we describe a general approach to designing transmembrane β-barrel pores with different diameters and pore geometries. Nuclear magnetic resonance and crystallographic characterization show that the designs are stably folded with structures resembling those of the design models. The designs have distinct conductances that correlate with their pore diameter, ranging from 110 picosiemens (~0.5 nanometer pore diameter) to 430 picosiemens (~1.1 nanometer pore diameter). Our approach opens the door to the custom design of transmembrane nanopores for sensing and sequencing applications.
PubMed: 39024453
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

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