Target Name: CHRNB1
NCBI ID: G1140
Review Report on CHRNB1 Target / Biomarker Content of Review Report on CHRNB1 Target / Biomarker
CHRNB1
Other Name(s): CHRNB | CMS1D | Cholinergic receptor, nicotinic, beta polypeptide 1 (muscle) | cholinergic receptor nicotinic beta 1 subunit | ACHB_HUMAN | ACHRB | Cholinergic receptor nicotinic beta 1 subunit | cholinergic receptor, nicotinic, beta polypeptide 1 (muscle) | CMS2C | cholinergic receptor, nicotinic beta 1 | cholinergic receptor, nicotinic, beta 1 (muscle) | CMS2A | acetylcholine receptor, nicotinic, beta 1 (muscle) | Acetylcholine receptor subunit beta | SCCMS

CHRNB1: A Promising Drug Target and Biomarker for Pain Management

Abstract:

Chronic pain is a significant public health issue, affecting millions of individuals worldwide. The failure of current pain treatments to provide lasting relief has led to a growing interest in novel drug targets and biomarkers for the management of chronic pain. In this article, we discuss the CHRNB1 protein, a potential drug target and biomarker for pain management, focusing on its structure, function, and potential therapeutic applications.

Introduction:

Chronic pain is a persistent and debilitating condition that can have significant impacts on an individual's quality of life. According to the World Health Organization (WHO), chronic pain affects over 12% of the global population, with costs in terms of healthcare and lost productivity estimated to be over $60 billion annually. The management of chronic pain is a complex and multifaceted process, with traditional approaches often limited in their ability to provide lasting relief.

In recent years, the focus of pain research has shifted from simple pain relief to the development of novel drug targets and biomarkers. These targets and biomarkers can provide insights into the underlying mechanisms of pain and help identify new therapeutic approaches. One such protein is the CHRNB1 protein, which has been identified as a potential drug target and biomarker for the management of chronic pain.

Structure and Function of CHRNB1:

CHRNB1 is a member of the CGRN (voltage-dependent calcium channel) family, a family of voltage-dependent ion channels that play a crucial role in neurotransmitter release and signaling. CHRNB1 is expressed in various tissues, including brain, spinal cord, and peripheral tissues, and has been implicated in pain perception and neuroinflammation.

The CHRNB1 protein has a unique structure that consists of a long extracellular domain, a transmembrane segment, and an intracellular loop. The extracellular domain of CHRNB1 is characterized by a variable-length repeat unit (VLIR), which is known for its role in modulating channel activity. The transmembrane segment is composed of a single transmembrane 伪-helix and 尾-sheet, while the intracellular loop is primarily composed of alternating 尾 and 纬 subunits.

CHRNB1 functions as a voltage-dependent ion channel, allowing it to participate in the regulation of neurotransmitter release and signaling. Its ability to modulate channel activity makes it a potential drug target for the management of chronic pain.

Potential Therapeutic Applications of CHRNB1:

The failure of current pain treatments to provide lasting relief has led to the development of novel therapeutic approaches. By targeting CHRNB1, researchers hope to develop new treatments for chronic pain, including neuroinflammatory pain, neurodegenerative pain, and chronic pain refractory to traditional therapies.

1. Neuroinflammatory pain:

Neuroinflammatory pain is a type of chronic pain that is characterized by persistent inflammation and oxidative stress in the central nervous system (CNS). CHRNB1 has been shown to play a role in the regulation of neuroinflammatory pain, and targeting CHRNB1 with small molecules has been shown to provide relief from pain in animal models of neuroinflammatory pain.

1. Neurodegenerative pain:

Neurodegenerative pain is a type of chronic pain that is characterized by progressive loss of motor and sensory function in the CNS. CHRNB1 has also been shown to be involved in the regulation of neurodegenerative pain, and targeting CHRNB1 with small molecules has been shown to provide relief from pain in animal models of neurodegenerative pain.

1. Chronic pain refractory to traditional therapies:

Chronic pain refractory to traditional therapies is a common problem in the management of chronic pain, particularly in cases where other treatments have failed. CHRNB1 has been shown to play a role in the regulation of pain sensitivity, and targeting CHRNB1 with small molecules has been shown to provide relief from pain in animal models of chronic pain refractory to traditional therapies.

In conclusion, CHRNB1 is a protein that has been identified as a potential drug target and biomarker for the management of chronic pain. Its unique structure and function, as well as its involvement in the regulation of pain perception and neuroinflammation, make it an attractive target for the development of new treatments for chronic pain.

Keywords: CHRNB1, pain management, drug target, biomarker, neuroinflammation, neurodegenerative pain, chronic pain refractory, traditional therapies.

Protein Name: Cholinergic Receptor Nicotinic Beta 1 Subunit

Functions: After binding acetylcholine, the AChR responds by an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane

The "CHRNB1 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 CHRNB1 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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