کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
383783 660833 2013 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
A cluster-DEE-based strategy to empower protein design
موضوعات مرتبط
مهندسی و علوم پایه مهندسی کامپیوتر هوش مصنوعی
پیش نمایش صفحه اول مقاله
A cluster-DEE-based strategy to empower protein design
چکیده انگلیسی


• Clustering and DEE techniques are combined with a SAT problem representation of the CPD problem.
• A knowledge-based method is combined with an ab initio strategy.
• Integrated Artificial Intelligence techniques are useful tools for the CPD problem.
• The proposed method was tested with eight protein sequences.
• Analysis reveal that the proposed method presents accurate results.

The Medical and Pharmaceutical industries have shown high interest in the precise engineering of protein hormones and enzymes that perform existing functions under a wide range of conditions. Proteins are responsible for the execution of different functions in the cell: catalysis in chemical reactions, transport and storage, regulation and recognition control. Computational Protein Design (CPD) investigates the relationship between 3-D structures of proteins and amino acid sequences and looks for all sequences that will fold into such 3-D structure. Many computational methods and algorithms have been proposed over the last years, but the problem still remains a challenge for Mathematicians, Computer Scientists, Bioinformaticians and Structural Biologists. In this article we present a new method for the protein design problem. Clustering techniques and a Dead-End-Elimination algorithm are combined with a SAT problem representation of the CPD problem in order to design the amino acid sequences. The obtained results illustrate the accuracy of the proposed method, suggesting that integrated Artificial Intelligence techniques are useful tools to solve such an intricate problem.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Expert Systems with Applications - Volume 40, Issue 13, 1 October 2013, Pages 5210–5218
نویسندگان
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