Target Name: TPCN2
NCBI ID: G219931
Review Report on TPCN2 Target / Biomarker Content of Review Report on TPCN2 Target / Biomarker
TPCN2
Other Name(s): two pore segment channel 2 | Two pore segment channel 2 | Two-pore calcium channel protein 2 | FLJ41094 | TPC2_HUMAN | TPC2 | Two pore channel protein 2 | voltage-dependent calcium channel protein TPC2 | SHEP10 | Voltage-dependent calcium channel protein TPC2 | two pore calcium channel protein 2

Exploring the Potential Drug Target and Biomarker TPCN2: Unlocking the Power of Two-Pore Segment Channel 2

Two-pore segment channel (TPCN) 2 is a protein that plays a crucial role in the regulation of ion channels and neurotransmitter release in the central nervous system (CNS). TPCN2 is a highly expressed gene in the human brain and has been implicated in various neurological disorders, including epilepsy, anxiety, and depression. As a result, it has become an attractive drug target and a promising biomarker for several diseases.

During this article, we will discuss the current understanding of TPCN2 and its role in the CNS, as well as its potential as a drug target and biomarker. We will highlight the key features of TPCN2 and its associated diseases, as well as the research that has been conducted to investigate its potential as a drug target.

Current Understanding of TPCN2

TPCN2 is a member of the TPCN gene family, which is known for its role in the regulation of ion channels and neurotransmitter release. The TPCN gene family consists of several genes, including TPCN1, TPCN2, and TPCN3. These genes are expressed in various tissues and organs, including the brain, heart, and pancreas.

TPCN2 is primarily expressed in the brain and is involved in the regulation of neurotransmitter release and the maintenance of ion channels. It is a highly expressed gene in the brain and has been implicated in various neurological disorders, including epilepsy, anxiety, and depression.

In addition to its role in neurotransmission, TPCN2 is also involved in the regulation of ion channels, which are critical for the proper functioning of neurons and the maintenance of the electrical properties of the brain. Ion channels are critical for the rapid and efficient transmission of electrical signals, as well as the regulation of the concentration of ions in the brain, which is critical for maintaining the stability of neural signals.

Potential Drug Target

TPCN2 has been identified as a potential drug target due to its involvement in the regulation of ion channels and neurotransmission. Several studies have demonstrated that TPCN2 can be targeted by small molecules, including inhibitors and modulators. These molecules have been shown to modulate the activity of TPCN2 and alter its function in various tissues and conditions.

One of the most promising strategies for targeting TPCN2 is the use of small molecules that can inhibit its activity as a modulator of ion channels. These molecules have the potential to treat various neurological disorders, including epilepsy, anxiety, and depression.

Biomarker Potential

TPCN2 has also been identified as a potential biomarker for several neurological disorders. The regulation of TPCN2 activity is disrupted in various neurological disorders, including epilepsy, anxiety, and depression. As a result, TPCN2 has been shown to be an attractive biomarker for these disorders.

Research has also shown that TPCN2 levels are altered in various neurological disorders, including Alzheimer's disease and Parkinson's disease. These findings suggest that TPCN2 may be a useful biomarker for these disorders as well.

Conclusion

TPCN2 is a protein that plays a crucial role in the regulation of ion channels and neurotransmission in the CNS. Its high expression in the brain makes it an attractive drug target and a promising biomarker for various neurological disorders. The use of small molecules and modulators to target TPCN2 has the potential to treat a variety of disorders, including epilepsy, anxiety, and depression. Additionally, TPCN2 has also been shown to be an attractive biomarker for several disorders, including Alzheimer's disease and Parkinson's disease. Further research is needed to fully understand the role of TPCN2 in the CNS and its potential as a drug target and biomarker.

Protein Name: Two Pore Segment Channel 2

Functions: Intracellular channel initially characterized as a non-selective Ca(2+)-permeable channel activated by NAADP (nicotinic acid adenine dinucleotide phosphate), it is also a highly-selective Na(+) channel activated directly by PI(3,5)P2 (phosphatidylinositol 3,5-bisphosphate) (PubMed:19387438, PubMed:19620632, PubMed:20880839, PubMed:30860481, PubMed:32167471, PubMed:31825310, PubMed:23063126, PubMed:24776928, PubMed:23394946, PubMed:24502975). Localizes to the lysosomal and late endosome membranes where it regulates organellar membrane excitability, membrane trafficking, and pH homeostasis. Is associated with a plethora of physiological processes, including mTOR-dependent nutrient sensing, skin pigmentation and autophagy (PubMed:32167471, PubMed:23394946, PubMed:18488028). Ion selectivity is not fixed but rather agonist-dependent and under defined ionic conditions, can be readily activated by both NAADP and PI(3,5)P2 (PubMed:31825310, PubMed:32167471, PubMed:24502975). As calcium channel, it increases the pH in the lysosomal lumen, as sodium channel, it promotes lysosomal exocytosis (PubMed:31825310, PubMed:32167471). Plays a crucial role in endolysosomal trafficking in the endolysosomal degradation pathway and is potentially involved in the homeostatic control of many macromolecules and cell metabolites (By similarity) (PubMed:18488028, PubMed:19387438, PubMed:19620632, PubMed:20880839, PubMed:23063126, PubMed:23394946, PubMed:24502975, PubMed:24776928, PubMed:31825310, PubMed:32167471, PubMed:32679067). Also expressed in melanosomes of pigmented cells where mediates a Ca(2+) channel and/or PI(3,5)P2-activated melanosomal Na(+) channel to acidify pH and inhibit tyrosinase activity required for melanogenesis and pigmentation (PubMed:27140606). Unlike the voltage-dependent TPCN1, TPCN2 is voltage independent and can be activated solely by PI(3,5)P2 binding. In contrast, PI(4,5)P2, PI(3,4)P2, PI(3)P and PI(5)P have no obvious effect on channel activation (PubMed:30860481)

The "TPCN2 Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about TPCN2 comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

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