Haem carrier protein 1
| Putative type VI secretion protein | |||||||
|---|---|---|---|---|---|---|---|
| Identifiers | |||||||
| Organism | |||||||
| Symbol | EC042_4529 | ||||||
| Alt. symbols | HCP1 | ||||||
| Entrez | 12885448 | ||||||
| PDB | 4HKH | ||||||
| RefSeq (Prot) | WP_001007313.1 | ||||||
| UniProt | D3GUW0 | ||||||
| Other data | |||||||
| Chromosome | Genomic: 4.86 - 4.86 Mb | ||||||
| |||||||
Haem or Heme carrier protein 1 (HCP1) was originally identified as mediating heme-Fe transport although it later emerged that it was the SLC46A1 folate transporter.[2][3]
HCP1 is a protein found in the small intestine that plays a role in the absorption of dietary heme, a form of iron that is only found in animal products.[4][5][6] Heme is an important nutrient for the body, as it is a component of many proteins, including hemoglobin, which carries oxygen in the blood. HCP1 is the only known heme transporter expressed in the small intestine and is therefore unique in its function and expression pattern.[5] HCP1 is a transmembrane protein that is expressed in the brush-border membrane of the small intestine, where it binds to heme and transports it into the enterocyte.[5]
The absorptive cell of the small intestine. HCP1 is particularly important in situations where dietary iron intake is low, as it allows for the efficient absorption of heme iron. HCP1 is also expressed in other tissues, including the liver and bone marrow, where it may play a role in the uptake of heme for the production of heme-containing proteins. Dysfunction of HCP1 has been associated with a range of conditions, including iron-deficiency anemia and certain types of cancer.[7][5]
History
[edit]HCP1 is also known as proton-coupled folate transporter (PCFT), as it was initially identified as a transporter for folate, a type of vitamin B [8] However, subsequent studies revealed that HCP1 primarily functions as a heme transporter in the small intestine.[5]
Properties
[edit]HCP1 is a type of transmembrane protein that spans the membrane of the enterocyte in the small intestine. It has a large extracellular domain that binds to heme, as well as a smaller intracellular domain that interacts with protons to drive heme uptake. The body more easily absorbs heme iron than non-heme iron, which is found in plant-based foods. This is because heme iron is more bioavailable, meaning that the body can absorb and use it more efficiently. HCP1 plays a key role in the absorption of heme iron in the small intestine, particularly in situations where dietary iron intake is low. HCP1 expression is regulated by a number of factors, including iron status, dietary heme intake, and inflammation. Studies have shown that HCP1 expression is upregulated in response to low iron levels and decreased when iron levels are sufficient.[5]
Pathogenesis
[edit]Dysfunction of HCP1 has been associated with a range of conditions, including iron-deficiency anemia, thalassemia, and porphyria. HCP1 has also been implicated in the pathogenesis of certain types of cancer, including colorectal cancer and pancreatic cancer.[5][9][10] HCP1 is a promising target for the development of drugs that can modulate heme uptake and metabolism. Inhibitors of HCP1 have been developed as potential treatments for cancer, while activators of HCP1 may have therapeutic potential in the treatment of iron-deficiency anemia.[7]
structure
[edit]The structure of HCP1 is complex and involves interactions between multiple domains and regions of the protein. HCP1 is a transmembrane protein, a type of protein that spans the cell membrane with parts of it located both inside and outside of the cell. Spanning the membrane allows it to transport heme across the cell membrane.[7] HCP1 has a large extracellular domain that binds to heme with high affinity. This binding enables HCP1 to transport heme into the enterocyte in the small intestine.[5][7] HCP1 is a proton-coupled transporter meaning that HCP1 relies on a proton gradient across the cell membrane to transport heme into the enterocyte.[5] The proton gradient uses the energy of protons to move heme across the cell membrane.[7][5] While HCP1 is expressed in the small intestine, liver, and bone marrow, HCP1 is primarily expressed in the small intestine, where it plays a key role in heme absorption. In other tissues, such as the liver and bone marrow it may be involved in heme metabolism. HCP1 expression is regulated by iron status: HCP1 expression is upregulated in response to low iron levels and downregulated when iron levels are sufficient.[5] This regulation allows for efficient heme absorption in times of low iron intake.[5] Dysfunctional HCP1 has been associated with iron-deficiency anemia, thalassemia, and certain types of cancer.[5]
solubility
[edit]Haem Carrier Protein 1 (HCP1) is a membrane-bound protein that is embedded in the cell membrane. As such, it is not freely soluble in aqueous solutions like water. However, like other membrane proteins, using detergents, HCP1 can be solubilized and extracted from the cell membrane. Detergents are amphipathic molecules that have both hydrophobic and hydrophilic regions and can interact with both the membrane lipids and the protein molecules to solubilize them. The solubilization of HCP1 from the membrane requires careful selection of a suitable detergent and optimization of the conditions to preserve the protein's stability and activity. Common detergents used for the solubilization of membrane proteins include Triton X-100, dodecyl maltoside (DDM), and n-dodecyl-β-D-maltopyranoside (DDM). Once solubilized, HCP1 can be purified using various techniques, including chromatography and ultracentrifugation, to obtain a highly purified and homogeneous protein sample for further study. The solubility and stability of HCP1 can be affected by various factors, including pH, temperature, ionic strength, and the presence of other molecules or ligands that interact with the protein.[7][5] some studies suggest that L-arginine can upregulate the expression of HCP-1, which may increase the uptake of cationic amino acids such as L-arginine in various cell types[11]
similar/ Related protein
[edit]HCP1 is identical to the proton-coupled folate transporter (PCFT-SLC46A1).[3]
HCP1 is related to the Reduced Folate Carrier (RFC) SLC19A1.[3]
References
[edit]- ^ Douzi B, Spinelli S, Blangy S, Roussel A, Durand E, Brunet YR, Cascales E, Cambillau C (2014). "Crystal structure and self-interaction of the type VI secretion tail-tube protein from enteroaggregative Escherichia coli". PLOS ONE. 9 (2): e86918. Bibcode:2014PLoSO...986918D. doi:10.1371/journal.pone.0086918. PMC 3925092. PMID 24551044.
- ^ Nakai Y, Inoue K, Abe N, Hatakeyama M, Ohta KY, Otagiri M, Hayashi Y, Yuasa H (August 2007). "Functional characterization of human proton-coupled folate transporter/heme carrier protein 1 heterologously expressed in mammalian cells as a folate transporter". The Journal of Pharmacology and Experimental Therapeutics. 322 (2): 469–76. doi:10.1124/jpet.107.122606. PMID 17475902. S2CID 23277839.
- ^ a b c Zhao R, Aluri S, Goldman ID (February 2017). "The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: Hereditary folate malabsorption". Molecular Aspects of Medicine. 53: 57–72. doi:10.1016/j.mam.2016.09.002. PMC 5253092. PMID 27664775.
- ^ Tong Y, Guo M (January 2009). "Bacterial heme-transport proteins and their heme-coordination modes". Archives of Biochemistry and Biophysics. 481 (1): 1–15. doi:10.1016/j.abb.2008.10.013. PMC 2683585. PMID 18977196.
- ^ a b c d e f g h i j k l m n Shayeghi M, Latunde-Dada GO, Oakhill JS, Laftah AH, Takeuchi K, Halliday N, et al. (September 2005). "Identification of an intestinal heme transporter". Cell. 122 (5): 789–801. doi:10.1016/j.cell.2005.06.025. PMID 16143108. S2CID 9130882.
- ^ Latunde-Dada GO, Takeuchi K, Simpson RJ, McKie AT (December 2006). "Haem carrier protein 1 (HCP1): Expression and functional studies in cultured cells". FEBS Letters. 580 (30): 6865–6870. doi:10.1016/j.febslet.2006.11.048. PMID 17156779. S2CID 34763873.
- ^ a b c d e f Krishnamurthy P, Xie T, Schuetz JD (June 2007). "The role of transporters in cellular heme and porphyrin homeostasis". Pharmacology & Therapeutics. 114 (3): 345–358. doi:10.1016/j.pharmthera.2007.02.001. PMID 17368550.
- ^ Yasuda S, Hasui S, Kobayashi M, Itagaki S, Hirano T, Iseki K (February 2008). "The mechanism of carrier-mediated transport of folates in BeWo cells: the involvement of heme carrier protein 1 in placental folate transport". Bioscience, Biotechnology, and Biochemistry. 72 (2): 329–334. doi:10.1271/bbb.70347. PMID 18256483. S2CID 10650884.
- ^ Ito H, Matsui H, Tamura M, Majima HJ, Indo HP, Hyodo I (July 2014). "Mitochondrial reactive oxygen species accelerate the expression of heme carrier protein 1 and enhance photodynamic cancer therapy effect". Journal of Clinical Biochemistry and Nutrition. 55 (1): 67–71. doi:10.3164/jcbn.14-27. PMC 4078070. PMID 25120282.
- ^ Hiyama K, Matsui H, Tamura M, Shimokawa O, Hiyama M, Kaneko T, et al. (2013-01-01). "Cancer cells uptake porphyrins via heme carrier protein 1". Journal of Porphyrins and Phthalocyanines. 17 (1n02): 36–43. doi:10.1142/S1088424612501192. ISSN 1088-4246.
- ^ Kurokawa H, Ito H, Terasaki M, Matano D, Taninaka A, Shigekawa H, Matsui H (2019-09-12). "Nitric oxide regulates the expression of heme carrier protein-1 via hypoxia inducible factor-1α stabilization". PLOS ONE. 14 (9): e0222074. Bibcode:2019PLoSO..1422074K. doi:10.1371/journal.pone.0222074. PMC 6742216. PMID 31513628.