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13th International Conference on Membrane Computing - MTA Sztaki

13th International Conference on Membrane Computing - MTA Sztaki

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<str<strong>on</strong>g>13th</str<strong>on</strong>g> <str<strong>on</strong>g>Internati<strong>on</strong>al</str<strong>on</strong>g> <str<strong>on</strong>g>C<strong>on</strong>ference</str<strong>on</strong>g> <strong>on</strong> <strong>Membrane</strong> <strong>Computing</strong>, CMC13,<br />

Budapest, Hungary, August 28 - 31, 2012. Proceedings, pages 407 - 418.<br />

Observer/Interpreter P Systems<br />

Dragos Sburlan<br />

Ovidius University of C<strong>on</strong>stanta<br />

Faculty of Mathematics and Informatics<br />

C<strong>on</strong>stanta, Mamaia 124, Romania<br />

Abstract. In this paper we discuss Observer/Interpreter P systems,<br />

i.e., a model of computati<strong>on</strong> inspired by the possibility of tracking and<br />

detecting fluorescent proteins in living cells and interpreting the results<br />

by visualizing molecular events in real time. In this regard, we define<br />

Observer/Interpreter P systems as a couple of two independent systems:<br />

a P system with symbol objects and multiset rewriting rules and a finite<br />

state machine able to perform an operati<strong>on</strong> (additi<strong>on</strong>/subtracti<strong>on</strong>) <strong>on</strong><br />

a register. We investigate the computati<strong>on</strong>al power of the model when<br />

different features are taking into account.<br />

Keywords: P Systems, Observati<strong>on</strong>, Interpretati<strong>on</strong><br />

1 Introducti<strong>on</strong><br />

One important breakthrough in the study of living cells was the possibility to<br />

label proteins for imaging use. This was achieved by using some genetically encoded<br />

fluorescent fusi<strong>on</strong> tags (for instance, the Nobel Prize in Chemistry in 2008<br />

was awarded to Osamu Shimomura, Martin Chalfie and Roger Tsien for the<br />

discovery and development of green fluorescent protein – GFP, that was used<br />

by researchers to study the development of nerve cells in the brain or how cancer<br />

cells spread). The gene for GFP was originally isolated from the jellyfish,<br />

Aequorea victoria, and since then, a lot of scientific effort has been focused <strong>on</strong><br />

the discovery of processes occurring inside cells. By visualizing molecular events<br />

happening within the living cells <strong>on</strong>e can trace the molecules functi<strong>on</strong> and regulati<strong>on</strong>.<br />

In general, the comm<strong>on</strong> methods for labeling molecules in biological<br />

systems are based <strong>on</strong> the genetic fusi<strong>on</strong> of fluorescent tags. Using these tags <strong>on</strong>e<br />

can watch at nanometer scale the behavior of molecules (the movement, positi<strong>on</strong>s,<br />

and interacti<strong>on</strong>s), hence <strong>on</strong>e can unravel the regulatory mechanisms of<br />

biological systems.<br />

Nowadays, the code for GFP can be inserted at any given positi<strong>on</strong> in the<br />

genome and <strong>on</strong>ce there, it will act as a label for the other genes around it.<br />

Accordingly, <strong>on</strong>e can place a GFP gene next to a given gene of interest and then<br />

study how the corresp<strong>on</strong>ding protein behaves by watching the green fluorescence.<br />

Moreover, the sequence of aminoacids in the GFP can be genetically engineered<br />

such that it will produce fluorescent proteins glowed in many different colors.<br />

In this way, several distinct types of proteins can be marked by different colors,<br />

407

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