Physics:Uniporter

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Comparison of transport proteins

Uniporters, also known as solute carriers or facilitated transporters, are a type of membrane transport protein that passively transports solutes (small molecules, ions, or other substances) across a cell membrane.[1] It uses facilitated diffusion for the movement of solutes down their concentration gradient from an area of high concentration to an area of low concentration.[2] Unlike active transport, it does not require energy in the form of ATP to function. Uniporters are specialized to carry one specific ion or molecule and can be categorized as either channels or carriers.[3] Facilitated diffusion may occur through three mechanisms: uniport, symport, or antiport. The difference between each mechanism depends on the direction of transport, in which uniport is the only transport not coupled to the transport of another solute.[4]

Uniporter carrier proteins work by binding to one molecule or substrate at a time. Uniporter channels open in response to a stimulus and allow the free flow of specific molecules.[2]

There are several ways in which the opening of uniporter channels may be regulated:

  1. Voltage – Regulated by the difference in voltage across the membrane
  2. Stress – Regulated by physical pressure on the transporter (as in the cochlea of the ear)
  3. Ligand – Regulated by the binding of a ligand to either the intracellular or extracellular side of the cell

Uniporters are found in mitochondria, plasma membranes and neurons.The uniporter in the mitochondria is responsible for calcium uptake.[1] The calcium channels are used for cell signaling and triggering apoptosis. The calcium uniporter transports calcium across the inner mitochondrial membrane and is activated when calcium rises above a certain concentration.[5] The amino acid transporters function in transporting neutral amino acids for neurotransmitter production in brain cells.[6] Voltage-gated potassium channels are also uniporters found in neurons and are essential for action potentials.[7] This channel is activated by a voltage gradient created by sodium-potassium pumps. When the membrane reaches a certain voltage, the channels open, which depolarizes the membrane, leading to an action potential being sent down the membrane.[8] Glucose transporters are found in the plasma membrane and play a role in transporting glucose. They help to bring glucose from the blood or extracellular space into cells usually to be utilized for metabolic processes in generating energy.[9]

Uniporters are essential for certain physiological processes in cells, such as nutrient uptake, waste removal, and maintenance of ionic balance.

Discovery

Facilitated diffusion using transport proteins

Early research in the 19th and 20th centuries on osmosis and diffusion provided the foundation for understanding the passive movement of molecules across cell membranes.[10]

In 1855, the physiologist Adolf Fick was the first to define osmosis and simple diffusion as the tendency for solutes to move from a region of higher concentration to a lower concentration, also very well-known as Fick's Laws of Diffusion.[11] Through the work of Charles Overton in the 1890s, the concept that the biological membrane is semipermeable became important to understanding the regulation of substances in and out of the cells.[11] The discovery of facilitated diffusion by Wittenberg and Scholander suggested that proteins in the cell membrane aid in the transport of molecules.[12] In the 1960s - 1970s, studies on the transport of glucose and other nutrients highlighted the specificity and selectivity of membrane transport proteins.[13]

Technological advancements in biochemistry helped isolate and characterize these proteins from cell membranes. Genetic studies on bacteria and yeast identified genes responsible for encoding transporters. This led to the discovery of glucose transporters (GLUT proteins), with GLUT1 being the first to be characterized.[14] Identification of gene families encoding various transporters, such as solute carrier (SLC) families, also advanced knowledge on uniporters and its functions.[14]

Newer research is focusing on techniques using recombinant DNA technology, electrophysiology and advanced imaging to understand uniporter functions. These experiments are designed to clone and express transporter genes in host cells to further analyze the three-dimensional structure of uniporters, as well as directly observe the movement of ions through proteins in real-time.[14] The discovery of mutations in uniporters has been linked to diseases such as GLUT1 deficiency syndrome, cystic fibrosis, Hartnup disease, primary hyperoxaluria and hypokalemic periodic paralysis.[15]

Types

Glucose transporter (GLUTs)

The glucose transporter (GLUTs) is a type of uniporter responsible for the facilitated diffusion of glucose molecules across cell membranes.[9]Glucose is a vital energy source for most living cells, however, due to its large size, it cannot freely move through the cell membrane.[16] The glucose transporter is specialized in transporting glucose specifically across the membrane. The GLUT proteins have several types of isoforms, each distributed in different tissues and exhibiting different kinetic properties.[16]

Glucose transporter

GLUTs are integral membrane proteins composed of 12 α-helix membrane spanning regions.[16] The GLUT proteins are encoded by the SLC2 genes and categorized into three classes based on amino acid sequence similarity.[17] Humans have been found to express fourteen GLUT proteins. Class I GLUTs include GLUT1, one of the most studied isoforms, and GLUT2.[16] GLUT1 is found in various tissues like the red blood cells, brain, and blood-brain barrier and is responsible for basal glucose uptake.[16] GLUT2 is predominantly found in the liver, pancreas, and small intestines.[16] It plays an important role in insulin secretion from pancreatic beta cells. Class II includes the GLUT3 and GLUT4.[16] GLUT3, primarily found in the brain, neurons and placenta, has a high affinity for glucose in facilitating glucose uptake into neurons.[16] GLUT4 plays a role in insulin-regulated glucose uptake and is mainly found in insulin-sensitive tissues such as muscle and adipose tissue.[16] Class III includes GLUT5, found in the small intestine, kidney, testes, and skeletal muscle.[16] Unlike the other GLUTs, GLUT5 specifically transports fructose rather than glucose.[16]

Glucose transporters allow glucose molecules to move down their concentration gradient from areas of high glucose concentration to areas of low concentration. This process often involves bringing glucose from the extracellular space or blood into the cell. The concentration gradient set up by glucose concentrations fuels the process without the need for ATP.[18]

When glucose binds to the glucose transporter, the protein channels change shape and undergo a conformational change to transport the glucose across the membrane. Once the glucose unbinds, the protein returns to its original shape. The glucose transporter is essential for carrying out physiological processes that require high energy demands in the brain, muscles, and kidneys by providing an adequate amount of energy substrate for metabolism. Diabetes, an example of a condition that involves glucose metabolism, highlights the importance of the regulation of glucose uptake in disease management.[19]

Mitochondrial Ca2+ iniporter (MCU)

The mitochondrial calcium uniporter (MCU) is a protein complex located in the inner mitochondrial matrix that functions to take up calcium ions (Ca2+) into the matrix from the cytoplasm.[20] The transport of calcium ions is specifically used in cellular function for regulating energy production in the mitochondria, cytosolic calcium signaling, and cell death. The uniporter becomes activated when cytoplasmic levels of calcium rise above 1 uM.[20]

The MCU complex comprises 4 parts: the port-forming subunits, regulatory subunits MICU1 and MICU2, and an auxiliary subunit, EMRE.[21] These subunits work together to regulate the uptake of calcium in the mitochondria. Specifically, the EMRE subunit functions for the transport of calcium, and the MICU subunit functions in tightly regulating the activity of MCU to prevent the overload of calcium concentrations in the cytoplasm.[21] Calcium is fundamental for signaling pathways in cells, as well as for cell death pathways.[21] The function of the mitochondrial uniporter is critical for maintaining cellular homeostasis.

The MICU1 and MICU2 subunits are a heterodimer connected by a disulfide bridge.[20] When there are high levels of cytoplasmic calcium, the MICU1-MICU2 heterodimer undergoes a conformational change.[20] The heterodimer subunits have cooperative activation, which means Ca2+ binding to one MICU subunit in the heterodimer induces a conformational change on the other MICU subunits. The uptake of calcium is balanced by the sodium-calcium exchanger.[21]

Large neutral amino acid transporter (LAT1)

SLC3 protein coding gene for LAT1

The L-type amino acid transporter (LAT1) is a uniporter that mediates the transport of neutral amino acids like L-tryptophan, leucine, histidine, proline, alanine, etc.[6] LAT1 favors the transport of amino acids with large branched or aromatic side chains. The amino acid transporter functions to move essential amino acids into the intestinal epithelium, placenta, and blood-brain barrier for cellular processes such as metabolism and cell signaling.[22] The transporter is of particular significance in the central nervous system as it provides the necessary amino acids for protein synthesis and neurotransmitter production in brain cells.[22] Aromatic amino acids like phenylalanine and tryptophan are precursors for neurotransmitters like dopamine, serotonin, and norepinephrine.[22]

LAT1 is a membrane protein of the SLC7 family of transporters and works in conjunction with the SLC3 family member 4F2hc to form a heterodimeric complex known as the 4F2hc complex.[6] The heterodimer consists of a light chain and a heavy chain covalently bonded by a disulfide bond. The light chain is the one that carries out transport, while the heavy chain is needed to stabilize the dimer.[6]

There is some controversy over whether LAT1 is an uniporter or an antiporter. The transporter has uniporter characteristics of transporting amino acids into cells in a unidirectional manner down the concentration gradient. However, recently it has been found that the transporter has antiporter characteristics of exchanging neutral amino acids for abundant intracellular amino acids.[23] Over-expression of LAT1 has been found in human cancer and is associated with playing a role in cancer metabolism.[24]

Equilibrative nucleoside transporters (ENTs)

The nucleoside transporters, or equilibrative nucleoside transporters, are uniporters that transport nucleosides, nucleobases, and therapeutic drugs across the cell membrane.[25] Nucleosides serve as building blocks for nucleic acid synthesis and are key components for energy metabolism in creating ATP/ GTP.[26] They also act as ligands for purinergic receptors such as adenosine and inosine. ENTs allow the transport of nucleosides down their concentration gradient. They also have the ability to deliver nucleoside analogs to intracellular targets for the treatment of tumors and viral infections.[26]

ENTs are part of the Major Facilitator Superfamily (MFS) and are suggested to transport nucleosides using a clamp-and-switch model.[26] In this model, the substrate first binds to the transporter, which leads to a conformational change that forms an occluded state (clamp). Then, the transporter switches to face the other side of the membrane and releases the bound substrate (switching).[26]

ENTs have been found in protozoa and mammals. In humans, they have been discovered as ENT3 (hENT1-3) and ENT4 (hENT4) transporters.[25] ENTs are expressed across all tissue types, but certain ENT proteins have been found to be more abundant in specific tissues. hENT1 is found mostly in the adrenal glands, ovary, stomach and small intestines.[25] hENT2 is expressed mostly in neurological tissues and small parts of the skin, placenta, urinary bladder, heart muscle and gallbladder.[25] hENT3 is expressed highly in the cerebral cortex, lateral ventricle, ovary and adrenal gland.[25] hENT4 is more commonly known as the plasma membrane monoamine transporter (PMAT), as it facilitates the movement of organic cations and biogenic amines across the membrane.[25]

Mechanism

Mechanism of uniport transport across cell membrane

Uniporters work to transport molecules or ions by passive transport across a cell membrane down its concentration gradient.

Upon binding and recognition of a specific substrate molecule on one side of the uniporter membrane, a conformational change is triggered in the transporter protein.[27] This causes the transporter protein to change its three-dimensional shape, which ensures the substrate molecule is captured within the transporter proteins structure. The conformational change leads to the translocation of the substrate across the membrane onto the other side.[27] On the other side of the membrane, the uniporter undergoes another conformational change in the release of the substrate molecule. The uniporter returns to its original conformation to bind another molecule for transport.[27]

Unlike symporters and antiporters, uniporters transport one molecule/ion in a single direction based on the concentration gradient.[28] The entire process depends on the substrate's concentration difference across the membrane to be the driving force for the transport by uniporters.[28] Cellular energy in the form of ATP is not required for this process.[28]

Physiological processes

Uniporters play an essential role in carrying out various cellular functions. Each uniporter is specialized to facilitate the transport of a specific molecule or ion across the cell membrane. Examples of a few of the physiological roles uniporters aid in include:[29]

  1. Nutrient Uptake: Uniporters facilitate the transport of essential nutrients into the cell. Glucose transporters (GLUTs) are uniporters that uptake glucose for energy production.[29]
  2. Ion homeostasis: Uniporters facilitate in maintaining the balance of ions (i.e., Na+, K+, Ca2+, Cl-) within cells [30]
  3. Metabolism: Uniporters are involved in the transport of essential ions, amino acids and molecules required for the metabolic pathway, protein synthesis and energy production[20]
  4. Cell signaling: Calcium uniporters help regulate intercellular calcium levels essential for signal transduction[1]
  5. Waste removal: Uniporters aid in removing metabolic waste products and toxins from cells
  6. pH regulation: Transport of ions by uniporters also helps to maintain the overall acid-base balance within cells [31]

Mutations

Mutations in genes encoding uniporters lead to dysfunctional transporter proteins being formed. This loss of function in uniporters causes disruption in cellular function which leads to various diseases and disorders.

Gene with mutation Disease Result of disease
Mutations in the SLC2A1 gene which encode glucose transporters (GLUTs) [32] GLUT1 Deficiency Syndrome[32] Impaired glucose transport across the blood-brain barriers, and neurological symptoms such as seizures, development delay, and movement disorders [33]
Mutations in the CFTR gene encoding ion channels[32] Cystic Fibrosis[32] Problems with breathing and digestion due to thick mucus forming; affects multiple organs, primarily the lungs and digestive system [33]
Mutation in KCNA1 gene encoding potassium channels[32] Hypokalemic Periodic Paralysis[32] Periodic muscle weakness; associated with low potassium levels due to altered transport activity [33]
Mutations in the SLC6A19 gene encoding amino acid transporter [32] Hartnup Disease[32] Impaired absorption of certain amino acid in the intestines and kidneys [33]
Mutations in the AGXT gene encoding peroxisomal membrane transporter [32] Primary Hyperoxaluria[32] Metabolic disease; Leads to accumulation of oxalate in causing kidney stone and damage [33]

See also

References

  1. ↑ 1.0 1.1 1.2 Zhang XC, Han L. Uniporter substrate binding and transport: reformulating mechanistic questions. Biophys Rep. 2016;2(2):45-54. doi: 10.1007/s41048-016-0030-7. Epub 2016 Oct 27. PMID 28018963; PMCID: PMC5138270.
  2. ↑ 2.0 2.1 Alberts, Bruce et al. — Essential Cell Biology, 1st edition. Garland Publishing, New York: 1998.
  3. ↑ Michael G. Wolfersberger; Uniporters, Symporters and Antiporters. J Exp Biol 1 November 1994; 196 (1): 5–6. doi: https://doi.org/10.1242/jeb.196.1.5
  4. ↑ Pratt CA, Voet D, Voet JG (2002). Fundamentals of biochemistry upgrade. New York: Wiley. pp. 264–266. ISBN 0-471-41759-9.
  5. ↑ Hoppe, U. (2010). "Mitochondrial Calcium Channels". FEBS Letters 584 (10): 1975–1981. doi:10.1016/j.febslet.2010.04.017. PMID 20388514. 
  6. ↑ 6.0 6.1 6.2 6.3 Häfliger P, Charles RP. The L-Type Amino Acid Transporter LAT1-An Emerging Target in Cancer. Int J Mol Sci. 2019 May 16;20(10):2428. doi: 10.3390/ijms20102428. PMID 31100853; PMCID: PMC6566973.
  7. ↑ Kim DM, Nimigean CM. Voltage-Gated Potassium Channels: A Structural Examination of Selectivity and Gating. Cold Spring Harb Perspect Biol. 2016 May 2;8(5):a029231. doi: 10.1101/cshperspect.a029231. PMID 27141052; PMCID: PMC4852806.
  8. ↑ OpenStax College (2013). Chapter 12.4 The Action Potential. OpenStax College. pp. 523–531. ISBN 978-1938168130. 
  9. ↑ 9.0 9.1 Olson AL, Pessin JE (1996). "Structure, function, and regulation of the mammalian facilitative glucose transporter gene family". Annual Review of Nutrition. 16: 235–56. doi:10.1146/annurev.nu.16.070196.001315. PMID 8839927.
  10. ↑ Cooper GM. The Cell: A Molecular Approach. 2nd edition. Sunderland (MA): Sinauer Associates; 2000. Transport of Small Molecules. Available from: https://www.ncbi.nlm.nih.gov/books/NBK9847/
  11. ↑ 11.0 11.1 Stillwell W. Membrane Transport. An Introduction to Biological Membranes. 2016:423–51. doi: 10.1016/B978-0-444-63772-7.00019-1. Epub 2016 Jul 15. PMCID: PMC7182109.
  12. ↑ Rubinow SI, Dembo M (April 1977). "The facilitated diffusion of oxygen by hemoglobin and myoglobin". Biophys. J. 18 (1): 29–42. Bibcode:1977BpJ....18...29R. doi:10.1016/S0006-3495(77)85594-X. PMC 1473276. PMID 856316
  13. ↑ Biology of Human Sodium Glucose Transporters Ernest M. Wright, Donald D. F. Loo, and Bruce A. Hirayama Physiological Reviews 2011 91:2, 733-794
  14. ↑ 14.0 14.1 14.2 Thorens B, Mueckler M. Glucose transporters in the 21st Century. Am J Physiol Endocrinol Metab. 2010 Feb;298(2):E141-5. doi: 10.1152/ajpendo.00712.2009. Epub 2009 Dec 15. PMID 20009031; PMCID: PMC2822486.
  15. ↑ Shamseldin HE, Alasmari A, Salih MA, Samman MM, Mian SA, Alshidi T, Ibrahim N, Hashem M, Faqeih E, Al-Mohanna F, Alkuraya FS. A null mutation in MICU2 causes abnormal mitochondrial calcium homeostasis and a severe neurodevelopmental disorder. Brain. 2017 Nov 1;140(11):2806-2813. doi: 10.1093/brain/awx237. PMID 29053821.
  16. ↑ 16.00 16.01 16.02 16.03 16.04 16.05 16.06 16.07 16.08 16.09 16.10 Navale AM, Paranjape AN. Glucose transporters: physiological and pathological roles. Biophys Rev. 2016 Mar;8(1):5-9. doi: 10.1007/s12551-015-0186-2. Epub 2016 Jan 19. PMID 28510148; PMCID: PMC5425736.
  17. ↑ Mueckler M, Thorens B. The SLC2 (GLUT) family of membrane transporters. Mol Aspects Med. 2013 Apr-Jun;34(2-3):121-38. doi: 10.1016/j.mam.2012.07.001. PMID 23506862; PMCID: PMC4104978.
  18. ↑ Carruthers, A. (1990). "Facilitated diffusion of glucose". Physiological Reviews. 70 (4): 1135–1176. doi:10.1152/physrev.1990.70.4.1135. ISSN 0031-9333. PMID 2217557.
  19. ↑ Jiang S, Young JL, Wang K, Qian Y, Cai L. Diabetic‑induced alterations in hepatic glucose and lipid metabolism: The role of type 1 and type 2 diabetes mellitus (Review). Mol Med Rep. 2020 Aug;22(2):603-611. doi: 10.3892/mmr.2020.11175. Epub 2020 May 22. PMID 32468027; PMCID: PMC7339764.
  20. ↑ 20.0 20.1 20.2 20.3 20.4 De Stefani D, Patron M, Rizzuto R. Structure and function of the mitochondrial calcium uniporter complex. Biochim Biophys Acta. 2015 Sep;1853(9):2006-11. doi: 10.1016/j.bbamcr.2015.04.008. Epub 2015 Apr 18. PMID 25896525; PMCID: PMC4522341.
  21. ↑ 21.0 21.1 21.2 21.3 D'Angelo D, Rizzuto R. The Mitochondrial Calcium Uniporter (MCU): Molecular Identity and Role in Human Diseases. Biomolecules. 2023 Aug 25;13(9):1304. doi: 10.3390/biom13091304. PMID 37759703; PMCID: PMC10526485.
  22. ↑ 22.0 22.1 22.2 Bhutia YD, Mathew M, Sivaprakasam S, Ramachandran S, Ganapathy V. Unconventional Functions of Amino Acid Transporters: Role in Macropinocytosis (SLC38A5/SLC38A3) and Diet-Induced Obesity/Metabolic Syndrome (SLC6A19/SLC6A14/SLC6A6). Biomolecules. 2022 Jan 31;12(2):235. doi: 10.3390/biom12020235. PMID 35204736; PMCID: PMC8961558.
  23. ↑ Singh, N. and G.F. Ecker, Insights into the Structure, Function, and Ligand Discovery of the Large Neutral Amino Acid Transporter 1, LAT1. Int J Mol Sci, 2018. 19(5).
  24. ↑ Kanai Y. Amino acid transporter LAT1 (SLC7A5) as a molecular target for cancer diagnosis and therapeutics. Pharmacol Ther. 2022 Feb;230:107964. doi: 10.1016/j.pharmthera.2021.107964. Epub 2021 Aug 12. PMID 34390745.
  25. ↑ 25.0 25.1 25.2 25.3 25.4 25.5 Boswell-Casteel RC, Hays FA. Equilibrative nucleoside transporters-A review. Nucleosides Nucleotides Nucleic Acids. 2017 Jan 2;36(1):7-30. doi: 10.1080/15257770.2016.1210805. Epub 2016 Oct 19. PMID 27759477; PMCID: PMC5728162.
  26. ↑ 26.0 26.1 26.2 26.3 Hollenstein M. Nucleoside triphosphates--building blocks for the modification of nucleic acids. Molecules. 2012 Nov 15;17(11):13569-91. doi: 10.3390/molecules171113569. PMID 23154273; PMCID: PMC6268876.
  27. ↑ 27.0 27.1 27.2 Fan, M., Zhang, J., Tsai, CW. et al. Structure and mechanism of the mitochondrial Ca2+ uniporter holocomplex. Nature 582, 129–133 (2020). https://doi.org/10.1038/s41586-020-2309-6
  28. ↑ 28.0 28.1 28.2 Majumder P, Mallela AK, Penmatsa A. Transporters through the looking glass. An insight into the mechanisms of ion-coupled transport and methods that help reveal them. J Indian Inst Sci. 2018 Sep;98(3):283-300. doi: 10.1007/s41745-018-0081-5. PMID 30686879; PMCID: PMC6345361.
  29. ↑ 29.0 29.1 David R, Byrt CS, Tyerman SD, Gilliham M, Wege S. Roles of membrane transporters: connecting the dots from sequence to phenotype. Ann Bot. 2019 Sep 24;124(2):201-208. doi: 10.1093/aob/mcz066. PMID 31162525; PMCID: PMC6758574.
  30. ↑ Zhang R, Kang R, Klionsky DJ, Tang D. Ion Channels and Transporters in Autophagy. Autophagy. 2022 Jan;18(1):4-23. doi: 10.1080/15548627.2021.1885147. Epub 2021 Mar 3. PMID 33657975; PMCID: PMC8865261.
  31. ↑ Seifter JL, Chang HY. Extracellular Acid-Base Balance and Ion Transport Between Body Fluid Compartments. Physiology (Bethesda). 2017 Sep;32(5):367-379. doi: 10.1152/physiol.00007.2017. PMID 28814497.
  32. ↑ 32.0 32.1 32.2 32.3 32.4 32.5 32.6 32.7 32.8 32.9 MedlinePlus [Internet]. Bethesda (MD): National Library of Medicine (US); [updated 2020 Jun 24]. Noonan syndrome; [updated 2020 Jun 18; reviewed 2018 Jun 01; cited 2020 Jul 1]; [about 5 p.].
  33. ↑ 33.0 33.1 33.2 33.3 33.4 MedlinePlus [Internet]. Bethesda (MD): National Library of Medicine (US); [updated Jun 24; cited 2020 Jul 1].



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