Recombinant Human ATAD3B Protein: Biology & Research Guide
Recombinant Human ATAD3B Protein: Biology & Research Guide
Recombinant Human ATAD3B Protein is a mitochondria-associated AAA-ATPase family member that plays critical roles in mitochondrial membrane organization, dynamics, and cellular stress responses, making it a valuable tool for investigating mitochondrial biology and related disease mechanisms.
- Protein Name
- ATPase Family AAA Domain-Containing Protein 3B (ATAD3B)
- Species
- Human (Homo sapiens)
- Protein Family
- AAA-ATPase superfamily
- Subcellular Localization
- Mitochondrial inner membrane and intermembrane space
- Format
- Recombinant protein (refer to product datasheet for specific formulation details)
- Primary Research Applications
- Mitochondrial dynamics, apoptosis signaling, protein interaction studies, functional assays
- Related SKU
- rp372626
What Is ATAD3B? Gene, Protein, and Biological Context
ATAD3B (ATPase Family AAA Domain-Containing Protein 3B) is a member of the AAA-ATPase (ATPases Associated with diverse cellular Activities) superfamily, a large and functionally diverse group of enzymes that utilize ATP hydrolysis to drive conformational changes in substrate proteins. The human ATAD3B gene resides in a genomic cluster on chromosome 1p36 alongside the closely related paralogs ATAD3A and ATAD3C, a region that arose through segmental duplication events during primate evolution.
ATAD3B is anchored to the mitochondrial inner membrane via transmembrane domains, with its AAA-ATPase domain oriented toward the mitochondrial matrix and an N-terminal domain extending into the intermembrane space. This topology positions ATAD3B at an interface critical for regulating mitochondrial membrane architecture, nucleoid organization, and communication between mitochondria and the endoplasmic reticulum at mitochondria-associated membrane (MAM) contact sites.
Compared with the ubiquitously expressed ATAD3A, ATAD3B shows a more restricted expression pattern and has been identified as having distinct, sometimes antagonistic, functional roles. Research suggests that ATAD3B can modulate mitochondrial morphology and influence apoptotic pathways, underscoring its significance as a research target in cancer biology and neurodegenerative disease.
Molecular Functions and Mechanisms of Action
The primary biochemical activity of ATAD3B resides in its conserved AAA-ATPase domain, which enables ATP binding and hydrolysis. This enzymatic activity is thought to power mechanical work on protein substrates or membrane structures, consistent with the broader functions attributed to AAA-ATPase family members in remodeling macromolecular assemblies.
Key molecular functions attributed to ATAD3B include:
- Mitochondrial dynamics regulation: ATAD3B has been implicated in controlling mitochondrial morphology, influencing the balance between fusion and fission events that determine the shape and connectivity of the mitochondrial network within cells.
- Nucleoid organization: Members of the ATAD3 family interact with mitochondrial DNA (mtDNA) and associated proteins, suggesting a role in organizing the mitochondrial genome into nucleoid structures.
- Apoptosis modulation: ATAD3B has been linked to the regulation of apoptotic signaling. Some studies indicate that ATAD3B may interact with components of the Bcl-2 family or influence cytochrome c release, positioning it as a regulator of intrinsic apoptosis.
- MAM and ER-mitochondria communication: Through its N-terminal domain in the intermembrane space, ATAD3B may participate in tethering or signaling interactions at mitochondria-associated membrane contact sites, influencing calcium transfer and lipid metabolism.
Understanding these mechanisms requires high-purity recombinant protein suitable for in vitro biochemical assays, structural studies, and protein–protein interaction experiments.
Research Applications of Recombinant Human ATAD3B Protein
Recombinant Human ATAD3B Protein (SKU: rp372626) from Aladdin Scientific is produced to support a range of experimental workflows in cell biology, biochemistry, and translational research. Typical applications include:
- In vitro ATPase activity assays: Measurement of ATP hydrolysis kinetics to characterize inhibitors, activators, or mutation effects on enzymatic function.
- Protein–protein interaction studies: Co-immunoprecipitation, pull-down assays, and surface plasmon resonance (SPR) experiments to map interaction partners within mitochondrial protein complexes.
- Structural biology: Provision of purified protein for crystallography, cryo-electron microscopy, or small-angle X-ray scattering (SAXS) studies aimed at resolving the three-dimensional architecture of ATAD3B.
- Antibody development and validation: Use as an antigen standard for raising or validating antibodies targeting ATAD3B, ensuring specificity in immunoassays and immunohistochemistry.
- Cell-free reconstitution systems: Incorporation into liposome-based or membrane-reconstitution assays to study ATAD3B's influence on membrane remodeling in a defined biochemical system.
- Disease mechanism research: Investigation of ATAD3B's roles in cancer cell survival, neurodegeneration, and mitochondrial diseases where AAA-ATPase dysfunction has been implicated.
Researchers should consult the product datasheet for storage conditions, recommended working concentrations, and quality control specifications before experimental use.
ATAD3B in Disease and Translational Research Context
Growing evidence implicates ATAD3B dysregulation in several human disease contexts, making it an increasingly relevant target for both basic and translational research programs.
Cancer biology: The ATAD3 gene cluster on chromosome 1p36 is frequently altered in neuroblastoma and other cancers. ATAD3B expression changes have been correlated with tumor behavior, and its capacity to modulate apoptotic thresholds suggests potential relevance as a cancer biomarker or therapeutic target. Recombinant ATAD3B protein enables biochemical characterization of these interactions in a controlled setting.
Neurodegenerative diseases: Mitochondrial dysfunction is a hallmark of diseases such as Parkinson's disease, Alzheimer's disease, and amyotrophic lateral sclerosis (ALS). Because ATAD3B influences mitochondrial morphology and membrane integrity, it is positioned as a candidate contributing factor in mitochondrial pathology underlying neurodegeneration. Recombinant protein tools are essential for dissecting these mechanistic links.
Mitochondrial genetic diseases: Variants in ATAD3 family genes have been associated with early-onset mitochondrial disorders characterized by neurological and developmental deficits. Recombinant ATAD3B protein supports functional studies comparing wild-type with disease-associated variant proteins.
It is important to note that the precise molecular mechanisms and the full spectrum of ATAD3B's physiological and pathological roles are still under active investigation. Researchers should cross-reference primary literature and consult the Aladdin Scientific product datasheet for the most current validated applications.
Product Specification, Handling, and Quality Assurance
Aladdin Scientific's Recombinant Human ATAD3B Protein (SKU: rp372626) is manufactured under stringent quality control processes to ensure batch-to-batch consistency suitable for demanding research applications. The following general guidance applies; always defer to the current product datasheet for authoritative specifications:
- Purity: Recombinant proteins in this line are typically verified by SDS-PAGE and may be further assessed by HPLC or other orthogonal methods. Specific purity data should be confirmed on the product datasheet.
- Storage: Lyophilized or liquid formulations should be stored according to datasheet instructions, typically at −20 °C or −80 °C. Avoid repeated freeze-thaw cycles to preserve protein integrity and activity.
- Reconstitution: If lyophilized, reconstitute in the recommended buffer as specified in the datasheet. Allow the vial to equilibrate to room temperature before opening, and mix gently to avoid foaming.
- Endotoxin levels: For cell-based assays, endotoxin content is a critical specification. Consult the datasheet for LAL-tested endotoxin values.
- Functional validation: Where available, functional activity data (e.g., ATPase activity) are included in product documentation to confirm biological relevance of each lot.
For technical questions regarding experimental design or product compatibility, contact Aladdin Scientific's technical support team.
Frequently asked questions
What is the biological function of ATAD3B?
ATAD3B is a mitochondria-localized AAA-ATPase that contributes to mitochondrial membrane architecture, nucleoid organization, and the regulation of apoptotic signaling. It is closely related to ATAD3A but shows distinct and sometimes opposing functional roles, particularly in modulating mitochondrial morphology and cellular stress responses.
What research applications is Recombinant Human ATAD3B Protein suitable for?
Recombinant Human ATAD3B Protein is suitable for in vitro ATPase activity assays, protein–protein interaction studies (pull-down, co-IP, SPR), structural biology investigations, antibody development and validation, and research into mitochondrial dysfunction in cancer and neurodegeneration. Always verify compatibility with your specific assay by consulting the product datasheet.
How should Recombinant Human ATAD3B Protein be stored to maintain activity?
The protein should be stored according to the conditions specified in the current product datasheet, typically at −20 °C or −80 °C. Repeated freeze-thaw cycles should be avoided to preserve protein integrity and enzymatic activity. If the product is lyophilized, reconstitute using the recommended buffer immediately before use.
How does ATAD3B differ from ATAD3A?
Although ATAD3A and ATAD3B share high sequence homology and both localize to the mitochondrial inner membrane, they exhibit distinct expression profiles and functional roles. ATAD3A is ubiquitously expressed and considered essential for mitochondrial integrity, while ATAD3B has a more restricted expression pattern and has been reported to have functions that can antagonize those of ATAD3A, particularly in apoptosis regulation. The mechanistic basis for these differences remains an active area of research.
Is Recombinant Human ATAD3B Protein suitable for cell-based assays?
Suitability for cell-based assays depends on the endotoxin level and formulation of the specific lot. Please consult the product datasheet for endotoxin test results (LAL assay) and formulation details before use in cell culture applications. Contact Aladdin Scientific's technical support for guidance on cell-based experimental designs.
References
- Hubstenberger A, et al. ATAD3A and ATAD3B are vertebrate-specific mitochondrial proteins required for autophagy of lipid droplets and maintenance of mitochondrial morphology. Biochemistry and Cell Biology. 2010.
- Desai R, et al. ATAD3 gene cluster deletions cause cerebellar dysfunction associated with altered mitochondrial DNA and cholesterol metabolism. Brain. 2017.
- Cooper HM, et al. ATPase-deficient mitochondrial inner membrane protein ATAD3A disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia. Human Molecular Genetics. 2017.
- Fang HY, et al. ATAD3B is a mitophagy receptor mediating clearance of oxidative stress-induced damaged mitochondrial DNA. EMBO Journal. 2023.
Products are supplied for research and development use only. Not for use in humans, animals, diagnosis, or therapy.
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