Calcium-binding protein

From Wikipedia, the free encyclopedia
Jump to: navigation, search

Calcium-binding proteins are proteins that participate in calcium cell signalling pathways by binding to Ca2+, the calcium ion that plays an important role in many cellular processes. This calcium ion has unique specific domains that bind to Calcium binding proteins (CBP) and is known to be heterogenous. One of the functions of Calcium binding proteins is to regulate the amount of free (unbound) Ca2+ in the cytosol of the cell.[1] Regulation of Ca(2+) is known as Calcium homeostasis.

Types[edit]

Many different calcium-binding proteins exist, with different cellular and tissue distribution and involvement in specific functions. Calcium binding proteins also serve an important physiological role for cells.[2] The most ubiquitous Ca2+-sensing protein, found in all eukaryotic organisms including yeasts, is calmodulin. Intracellular storage and release of Ca2+ from the sarcoplasmic reticulum is associated with the high-capacity, low-affinity calcium-binding protein calsequestrin.[3] Calretinin is another type of Calcium binding protein weighing 29kD. It is involved in cell signaling and shown to exist in neurons. This type of protein is also found in large quantities in malignant mesothelial cells, which can be easily differentiated from carcinomas. This differentiation is later applied for a diagnosis on ovarian stromal tumors.[4] Also, another member of the EF-hand superfamily is the S100B protein, which regulates p53. P53 is known as a tumor suppressor protein and in this case acts as a transcriptional activator or repressor of numerous genes. S100B proteins are abundantly found in cancerous tumor cells causing them to be overexpressed, therefore making these proteins useful for classifying tumors. In addition, this explains why this protein can easily interact with p53 when transcriptional regulation takes place.[5]

Ca(2+) binding proteins can be either intracellular and extracellular. Those that are intracellular can contain or lack a structural EF- hand domain. Extra cellular calcium binding proteins are classified into six groups.[6] Since Ca (2+) is an important second messenger, it can act as an activator or inhibitor in gene transcription. Those that belong to the EF-hand superfamily such as Calmodulin and Calcineurin have been linked to transcription regulation. When levels of Ca(2+) increase in the cell, these members of the EF-hand superfamily regulate transcription indirectly by phosphorylating/dephosphorylating transcription factors.[5]

Functions[edit]

With their role in signal transduction, calcium-binding proteins contribute to all aspects of the cell's functioning, from homeostasis to learning and memory. For example, the neuron-specific calexcitin has been found to have an excitatory effect on neurons, and interacts with proteins that control the firing state of neurons, such as the voltage-dependent potassium channel.[7]

Compartmentalization of calcium binding proteins such as calretinin and calbindin-28 kDa has been noted within cells, suggesting that these proteins perform distinct functions in localized calcium signaling.[8] It also indicates that in addition to freely diffusing through the cytoplasm to attain a homogeneous distribution, calcium binding proteins can bind to cellular structures through interactions that are likely important for their functions.[8]

Calcium-binding protein modulators[edit]

Calcium Binding Protein Modulator Agonists

Calcium Binding Protein Modulator Antagonists

Calcium Binding Protein Modulator Inhibitors

Additional Calcium Binding Protein Modulators

See also[edit]

References[edit]

  1. ^ Kinjo, Tashi G; Schnetkamp, Paul PM. Ca2+ Chemistry, Storage and Transport in Biologic Systems: An Overview. Madame Curie Bioscience Database [Internet]. Retrieved 2 May 2016. 
  2. ^ Yáñez M, Gil-Longo J, Campos-Toimil M (2012). "Calcium binding proteins.". Adv Exp Med Biol 740: 461–82. doi:10.1007/978-94-007-2888-2_19. PMID 22453954. 
  3. ^ Siegel, George (Ed.). Basic neurochemistry: molecular, cellular and medical aspects. Lippincott Williams and Wilkins / 1999 ISBN 0-397-51820-X
  4. ^ http://www.nordiqc.org/Epitopes/calretinin/calretinin.htm
  5. ^ a b http://nmr.uhnres.utoronto.ca/ikura/publication/PDF%20Articles/2002/The%20role%20of%20calcium%20binding%20proteins.pdf
  6. ^ http://download.springer.com/static/pdf/28/chp%253A10.1007%252F978-94-007-2888-2_19.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Fchapter%2F10.1007%2F978-94-007-2888-2_19&token2=exp=1462396956~acl=%2Fstatic%2Fpdf%2F28%2Fchp%25253A10.1007%25252F978-94-007-2888-2_19.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Fchapter%252F10.1007%252F978-94-007-2888-2_19*~hmac=0838af8d5cc7a124739099b49a84211059c2f5d7df52548bd38371e2027ffada
  7. ^ Nelson T, Cavallaro S, Yi C, McPhie D, Schreurs B, Gusev P, Favit A, Zohar O, Kim J, Beushausen S, Ascoli G, Olds J, Neve R, Alkon D (1996). "Calexcitin: a signaling protein that binds calcium and GTP, inhibits potassium channels, and enhances membrane excitability". PNAS 93 (24): 13808–13. doi:10.1073/pnas.93.24.13808. PMC 19433. PMID 8943017. 
  8. ^ a b Mojumder DK, Wensel TG, Frishman LJ (Aug 2008). "Subcellular compartmentalization of two calcium binding proteins, calretinin and calbindin-28 kDa, in ganglion and amacrine cells of the rat retina". Molecular Vision 14: 1600–1613. PMC 2528027. PMID 18769561. 

External links[edit]