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Protein Mediated Generation of Human Induced Pluripotent Cells for Maximum Efficiency

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Protein Mediated Generation of Human Induced Pluripotent Cells for Maximum Efficiency
Protein Mediated Generation of Human Induced Pluripotent Cells for Maximum Efficiency
Project ID: 3244K

Abstract
Inefficiency of IPS cell generation is a major obstacle in the development of IPS based technologies, such as their use in regenerative medicine. Current methods are limited to approximately 20% efficiency and often come with a trade off in safety. We propose a new technology that would increase the rate of IPS reprogramming to nearly 100%. This technology entails the usage of protein complexes in tandem with small mimicking chemical compounds to achieve this objective. The protein complex is bonded to elements that guide it to a universal nuclear antigen while the small mimicking compounds mimicked the intranuclear signaling of natural proteins responsible for inducing pluripotency.

Protein Mediated Generation of Human Induced Pluripotent Cells for Maximum Efficiency
Project ID: 3244K
Protein Mediated Generation of Human Induced Pluripotent Cells for Maximum Efficiency

Present Technology
Induced pluripotent stem cells (IPS) are pluripotent cells created from non-pluripotent cells. Pluripotent stem cells are cells that are able to differentiate into different kinds of cells and can divide indefinitely, and include embryonic stem cells. In fact, IPS cells are nearly equivalent to embryonic stem cells in form and function, having similar morphology, colony formation patterns, gene expression, and in vivo differentiation patterns. It was even found in 2007 that mouse IPS cells could be used to form viable chimeras. [3] That is, when IPS cells were injected into developing mouse embryos, the embryo developed in vivo and its live birth was successful.
Further studies show that such chimeras are able to mate with normal mice and also produce viable offspring. [4]

Several different methods have been developed to derive IPS cells from 2006 until now.
The original method utilized by the Kyoto team in 2006 was the use of a



Bibliography: [1] The UK Stem Cell Foundation (2011). STEM CELL RESEARCH History. [ONLINE] Available at: http://www.ukscf.org/research/history.html [2] The Nobel Assembly(2012) "The 2012 Nobel Prize in Physiology or Medicine - Press Release" http://www.nobelprize.org/nobel_prizes/medicine/laureates/2012/press.html [3] Keisuke Okita, Tomoko Ichisaka Shinya Yamanaka, (2007) Marvin A. Peters, Boris Brill, Bernd Groner, Ingolf Bach, Thorsten Heinzel and Martin Göttlicher, (2003) Chen, Whitney Muhlestein & Douglas A Melton, (2008). Induction of pluripotent stem cells from primary human fibroblasts with only Oct4 and Sox2 [7]Keisuke Okita, Masato Nakagawa, Hong Hyenjong, Tomoko Ichisaka, Shinya Yamanaka, (2008) 322 , pp.949-953 [8]Judson RL, Babiarz JE, Venere M, Blelloch R., (2009) [10] : H.Zhou, Wu.S, Joo JY, Zhu S, Han DW, Generation of Induced Pluripotent Stem Cells Using Recombinant Proteins, Cell Stem Cell (2009),doi:10.1016/j.stem.2009.04.005 [11](2009). Telomere Function. [ONLINE] Available at: http://www.newsmedical.net/health/Telomere-Function.aspx. [Last Accessed 1/16/13]. [12] Racaniello V (2009). The error-prone ways of RNA synthesis. [ONLINE] Available at: http://www.virology.ws/2009/05/10/the-error-prone-ways-of-rna-synthesis/ T.Hepatology. 2009 Mar; 49(3) ScienceMag:1048-9. Kiichiro Tomoda, Shinya Yamanaka,. Induction of Pluripotent Stem Cells from Adult Human Fibroblasts by Defined Factors, Cell (2007), doi:10.1016/j.cell.2007.11.01

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