技术文章

Recombinant Human HPDL Protein: Research Guide & Applications

Recombinant Human HPDL Protein is a recombinant form of the human 4-hydroxyphenylpyruvate dioxygenase-like (HPDL) enzyme, increasingly recognized for its critical role in mitochondrial function and implicated in early-onset neurological disorders.

Product Name
Recombinant Human HPDL Protein
SKU
rp367770
Gene Name
HPDL (4-hydroxyphenylpyruvate dioxygenase-like)
Species
Human (Homo sapiens)
Protein Class
Recombinant enzyme / mitochondrial protein
Primary Research Area
Mitochondrial biology, neurological disease, enzyme function

Biological Background of HPDL

HPDL (4-hydroxyphenylpyruvate dioxygenase-like protein) is a nuclear-encoded gene product that localizes to the mitochondria. It belongs to the broader family of iron- and 2-oxoglutarate-dependent dioxygenases, sharing structural homology with 4-hydroxyphenylpyruvate dioxygenase (HPD), an enzyme involved in tyrosine catabolism and coenzyme Q biosynthesis pathways.

Emerging research has identified HPDL as a mitochondria-targeted protein whose precise enzymatic substrate and catalytic mechanism remain subjects of active investigation. Loss-of-function variants in the HPDL gene have been associated with a spectrum of early-onset, autosomal recessive neurological conditions, including spastic paraplegia and hypomyelinating leukodystrophy in pediatric patients. These clinical observations suggest that HPDL plays a non-redundant and essential role in maintaining neuronal and mitochondrial integrity.

The recombinant human HPDL protein provides researchers with a purified, well-defined tool to investigate the biochemical properties, substrate specificity, and interaction partners of this protein under controlled in vitro conditions.

Protein Properties and Quality Considerations

Recombinant Human HPDL Protein (rp367770) is produced using recombinant expression systems to ensure batch-to-batch consistency and high purity suitable for demanding biochemical assays. When evaluating a recombinant protein for research use, the following quality attributes should be considered:

  • Purity: High-purity preparations (typically ≥90% by SDS-PAGE) minimize the risk of confounding results from contaminating proteins. Researchers should request a certificate of analysis (CoA) to verify lot-specific purity data.
  • Biological Activity: Confirmation of activity through functional assays, where available, ensures that the recombinant protein retains native-like enzymatic or binding properties.
  • Formulation and Stability: The buffer composition, presence of stabilizing agents (e.g., glycerol, BSA), and recommended storage temperature (typically -80°C for long-term storage) directly affect protein stability and experimental reproducibility.
  • Endotoxin Levels: For cell-based assays and in vivo applications, low endotoxin content is critical to prevent non-specific inflammatory responses.

Researchers are advised to consult the product datasheet and CoA for rp367770 for lot-specific specifications. Contact Aladdin Scientific technical support for additional characterization data if required.

Research Applications

Recombinant Human HPDL Protein (rp367770) is a versatile research reagent applicable across multiple experimental contexts:

  • Enzyme Characterization Studies: Investigate the substrate specificity, cofactor requirements (e.g., iron, 2-oxoglutarate), and kinetic parameters of HPDL in vitro. Such studies are essential for defining the precise biochemical role of this enzyme.
  • Protein-Protein Interaction Studies: Use purified HPDL protein in pull-down assays, co-immunoprecipitation controls, or surface plasmon resonance (SPR) experiments to identify and validate interaction partners within the mitochondrial proteome.
  • Antibody Validation: Recombinant HPDL protein serves as a positive control antigen for validating anti-HPDL antibodies in Western blotting, ELISA, and immunoprecipitation applications.
  • Structural Biology: High-purity recombinant protein preparations are suitable for crystallography, cryo-electron microscopy (cryo-EM), and other structural characterization approaches aimed at elucidating the three-dimensional structure of HPDL.
  • Disease Mechanism Research: Given the association of HPDL loss-of-function with pediatric neurological disorders, recombinant HPDL protein can be used to study pathogenic mechanisms, screen for small-molecule modulators, or develop diagnostic tools.
  • Coenzyme Q Biosynthesis Research: Given HPDL's homology to HPD and its mitochondrial localization, it may be a valuable tool in studying aspects of the CoQ biosynthesis pathway and related metabolic processes.

Ordering and Technical Support

Recombinant Human HPDL Protein is available from Aladdin Scientific under SKU rp367770. To place an order or request a quotation, visit the Aladdin Scientific website or contact your regional sales representative.

For technical inquiries regarding experimental design, recommended assay conditions, or interpretation of results with this product, please reach out to the Aladdin Scientific technical support team. Our scientists are available to assist with protocol optimization and troubleshooting.

Custom quantities, bulk orders, and special formulations may be available upon request. Please contact Aladdin Scientific customer service for further details on custom production options.

Reference internal product identifier: absea#PP-18234 (rp367770)

Frequently asked questions

What is the HPDL protein and why is it important for research?

HPDL (4-hydroxyphenylpyruvate dioxygenase-like protein) is a mitochondria-targeted enzyme sharing homology with HPD, an enzyme involved in tyrosine catabolism and coenzyme Q biosynthesis. Its importance in research stems from the discovery that loss-of-function mutations in the HPDL gene are associated with early-onset autosomal recessive neurological disorders, including spastic paraplegia and leukodystrophy, making it a key target for understanding mitochondrial and neuronal biology.

How should I store and handle Recombinant Human HPDL Protein (rp367770) to maintain activity?

Upon receipt, store Recombinant Human HPDL Protein at -80°C for long-term preservation. After reconstitution (if lyophilized), prepare single-use aliquots to avoid repeated freeze-thaw cycles, which can degrade protein integrity and reduce activity. Avoid vortexing; instead, gently pipette to mix. Always refer to the specific product datasheet for rp367770 for lot-specific storage and handling instructions.

What are the main applications for Recombinant Human HPDL Protein in the laboratory?

Recombinant Human HPDL Protein (rp367770) supports a wide range of research applications, including in vitro enzyme characterization, protein-protein interaction studies (e.g., pull-down and SPR assays), antibody validation in Western blot and ELISA, structural biology studies (crystallography, cryo-EM), and investigation of disease mechanisms underlying HPDL-associated neurological disorders. It may also be used in research exploring coenzyme Q biosynthesis and mitochondrial metabolism.

How do I determine the optimal working concentration of HPDL protein for my assay?

The optimal working concentration of Recombinant Human HPDL Protein must be determined empirically for each specific assay format and experimental system. It is recommended to conduct pilot experiments using a range of protein concentrations before committing to large-scale assays. Consult the product datasheet and contact Aladdin Scientific technical support for guidance specific to your application.

Can Recombinant Human HPDL Protein be used for in vivo studies?

While Recombinant Human HPDL Protein is primarily intended for in vitro research applications, its suitability for in vivo use depends on formulation, endotoxin levels, and specific experimental requirements. Researchers considering in vivo applications should verify endotoxin content from the certificate of analysis and consult Aladdin Scientific technical support to assess whether the product specification meets the requirements of their intended in vivo study.

References

  1. Aladdin Scientific Product Datasheet: Recombinant Human HPDL Protein, SKU rp367770 (absea#PP-18234).
  2. Wiessner M, et al. Bi-allelic variants in HPDL cause pure and complicated hereditary spastic paraplegia. Brain. 2021.
  3. Husain RA, et al. HPDL mutations cause a neurodegenerative condition with leukodystrophy. Brain. 2020.

Products are supplied for research and development use only. Not for use in humans, animals, diagnosis, or therapy.

目录: 技术文章

Da — 若无特别说明,分子量单位默认为道尔顿。   Mw — 重均分子量。   Mn — 数均分子量。

产品仅供科研与开发使用,不用于人体、动物、诊断或治疗。

引用本文

阿拉丁科学.《Recombinant Human HPDL Protein: Research Guide & Applications》. 阿拉丁知识库,更新于 2026年11月2日。 https://www.aladdin-e.com/zh_cn/faqs/recombinant-human-hpdl-protein-research-guide-en.html
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