Chemistry:Cm28
| Potassium channel toxin alpha-KTx 32.1 | |||||||
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| Identifiers | |||||||
| Organism | |||||||
| Symbol | C0HM22 | ||||||
| UniProt | C0HM22 | ||||||
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| Identifiers | |
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3D model (JSmol)
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| Properties | |
| C113H173N35O38S6 | |
| Molar mass | 2822.19 g·mol−1 |
| Related compounds | |
Related compounds
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ε-KTx1.1, ε-KTx1.2 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Cm28, a scorpion toxin from Centruroides margaritatus, selectively blocks voltage-gated potassium channels KV1.2 and KV1.3 with high affinity.[1] It also suppresses the activation of human CD4+ effector memory T cells, suggesting its potential as a therapeutic agent for autoimmune diseases. Phylogenetic analysis reveals that Cm28 belongs to a new α-KTx subfamily, highlighting its unique structural and functional properties for potential drug development.[1]
Etymology
The peptide name "Cm28" is derived from the scorpion species Centruroides margaritatus and its molecular mass, which is estimated to be 2820 Daltons.[1]
Sources
Cm28 was isolated from the venom of the Centruroides margaritatus scorpion. The venom was isolated through milking the animal by electric stimulation.[1]
Chemistry
Structure
Amino acid sequence
KCRECGNTSPSCYFSGNCVNGKCVCPA
Family
Phylogenetic analysis comparing the amino acid sequence of Cm28 with 75 other reported scorpion toxins suggests that Cm28 belongs to the α-KTx family. It has been given the systematic number α-KTx 32.1. Cm28 lacks the typical lysine-tyrosine functional dyad required for blocking KV channels.[1]
The 3D model can be found on Swissmodel.[3]
Target and mode of action
Cm28 is a potent inhibitor of voltage-gated potassium channels KV1.2[4] and KV1.3,[5] with dissociation constants (Kd) of 0.96 nM and 1.3 nM, respectively. KV1.3 channels are essential for the activation and proliferation of TH17 cells, a T helper cell subset critical for immune responses, especially in autoimmune diseases.[6] These channels regulate T cell proliferation and other signaling pathways necessary for T cell functioning. The binding of Cm28 to both KV1.2 and KV1.3 is reversible, allowing dynamic regulation of channel activity during immune responses.[1]
It operates by physically blocking the pores of these channels, preventing potassium ions from passing through. Rather than altering the voltage-sensing domain, Cm28 interacts with the selectivity filter region, effectively disrupting ion flow without shifting the activation thresholds.[1] This specific interaction highlights Cm28's precise targeting of the pore region, making it a highly selective blocker for KV1.2 and KV1.3 channels.[7] The exact residues involved in selectivity filter block are unknown.
Toxicity
In toxicity assays, Cm28 did not compromise the viability of human CD4+ T cells, even at concentrations much higher than its binding affinity to KV1.3 channels. Specifically, after a 24-hour incubation period with 1.5 μM Cm28, the cytotoxicity of the peptide on quiescent and TCR-activated CD4+ T cells was less than 1%. This finding was confirmed by both lactate dehydrogenase (LDH) assays and flow cytometry using Zombie NIR dye to evaluate cell viability. Therefore, Cm28 demonstrates minimal cytotoxicity in vitro under the experimental conditions.[1]
References
- ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 "Cm28, a scorpion toxin having a unique primary structure, inhibits KV1.2 and KV1.3 with high affinity". The Journal of General Physiology 154 (8). August 2022. doi:10.1085/jgp.202213146. PMID 35699659.
- ↑ "Potassium channel toxin alpha-KTx 32.1 - Centruroides margaritatus (Central American bark Scorpion)". UniProtKB. https://www.uniprot.org/uniprotkb?query=CM28.
- ↑ "C0HM22 | SWISS-MODEL Repository". https://swissmodel.expasy.org/repository/uniprot/C0HM22?csm=619126AE0255A0CA.
- ↑ "Channelpedia - Kv1.2". https://channelpedia.epfl.ch/ionchannels/2.
- ↑ "Channelpedia - Kv1.3". https://channelpedia.epfl.ch/ionchannels/3.
- ↑ "Venom components of the scorpion Centruroides limpidus modulate cytokine expression by T helper lymphocytes: Identification of ion channel-related toxins by mass spectrometry". International Immunopharmacology 84. July 2020. doi:10.1016/j.intimp.2020.106505. PMID 32380407.
- ↑ "Computational Studies of Venom Peptides Targeting Potassium Channels". Toxins 7 (12): 5194–211. December 2015. doi:10.3390/toxins7124877. PMID 26633507.
External links
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