9EYQ image
Deposition Date 2024-04-09
Release Date 2025-04-23
Last Version Date 2026-05-27
Entry Detail
PDB ID:
9EYQ
Keywords:
Title:
The structure of nonameric pore of RN1 variant of actinoporin Fav
Biological Source:
Source Organism(s):
Expression System(s):
Method Details:
Experimental Method:
Resolution:
3.28 Å
Aggregation State:
PARTICLE
Reconstruction Method:
SINGLE PARTICLE
Macromolecular Entities
Protein Blast
Polymer Type:polypeptide(L)
Molecule:Actinoporin
Chain IDs:A, B, C, D, E, F, G, H, I
Chain Length:193
Number of Molecules:9
Biological Source:Orbicella faveolata
Ligand Molecules
Primary Citation
High-Throughput Human Histone Detection by an Engineered Actinoporin Nanopore.
ACS Sens 11 2016 2029 (2026)
PMID: 41718555 DOI: 10.1021/acssensors.5c03533

Abstact

The use of protein nanopores has proven to be very promising for the identification of proteins or the sequencing of peptides. However, their widespread use in biosensor applications is limited by more complex molecular properties of proteins in comparison to nucleic acids. Here, we developed an alpha-helical Fav nanopore from the coral Orbicella faveolata to detect human histones using a commercial MinION device. The engineered nanopores showed stable insertion into the polymeric membrane support. Bulk analysis of several tens to hundreds of pores per measurement revealed significant differences in mean current passing the pore and current noise resulting from capturing different full-length human histones or their post-translationally modified variants into the pore lumen. Importantly, detailed blocking analyses confirmed histone-specific signals that allow further discrimination between two medically important extracellular histones in mixtures. The newly developed Fav nanopore and high-throughput approach for the detection of biomedically important proteins is an important step towards the widespread use of nanopores in modern analytics.

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Protein

Chemical

Disease

Primary Citation of related structures
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