Ras: Difference between revisions

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=== References:  ===
=== References:  ===


<references />
<references />Alberts, B., Johnson, A., Lewis, J., Raff, M., Roberts, K. and Walter, P. . (2008). Signalling through enzyme-coupled cell-surface receptors. In: Anderson, M. and Granum, S. Molecular Biology of The Cell. 5th ed. USA: Garland Science. 927.

Revision as of 20:57, 25 November 2014

The Ras protein is a monomeric G-protein with weak GTPase enzyme activity. It is a signal-transducer protein for growth factors and therefore it helps to transfer signals from cell-surface Receptor Tyrosine Kinase (RTK) receptors to the nucleus [1].

Active and Inactive forms of Ras

Ras is in its inactive form when it is bound to GDP, and becomes active once GDP has been exchanged for a GTP molecule. This reaction is initiated by the action of a specific signal molecule binding to a RTK receptor on the cell membrane. The activated RTK has intrinsic kinase activity, and this leads to phosphorylation of docking proteins at the RTK domains. The adaptor protein Grb-2 mediates the reaction between the RTK and Ras GEF, which exchanges GDP for GTP, acvtivating Ras which can transmit of a signal along multiple pathways. The inactivation of Ras is caused by the hydrolysis of GTP and it is mediated by Ras GAP. If the GTP bound at Ras cannot be hydrolysed then it would cause Ras to stay in an active form and thus lead to cancer.

References:

  1. Alberts, B, et al, 2008. Molecular Biology of the Cell. 5th ed. United States of America: Garland Science.

Alberts, B., Johnson, A., Lewis, J., Raff, M., Roberts, K. and Walter, P. . (2008). Signalling through enzyme-coupled cell-surface receptors. In: Anderson, M. and Granum, S. Molecular Biology of The Cell. 5th ed. USA: Garland Science. 927.