A Knowledge Discovery Method for the Characterization of Protein Unfolding Processes

• Tipo: Artigo em Livro de Atas de Conferência Internacional
• Data: 2009

Autores

Elisabeth Fernandes (Autor) Outra; Alipio M Jorge (Autor) FCUP; Candida G Silva (Autor) Outra; Rui M M Brito (Autor) Outra

Ata de Conferência Internacional

Título: ADVANCES IN SOFT COMPUTING

Páginas: 180-188

2nd International Workshop on Practical Applications of Computational Biology and Bioinformatics (IWPACBB 08)

Salamanca, SPAIN, OCT 22-24, 2008

Indexação

ISI Web of Knowledge - 1 Citação

Scopus - 0 Citações

Classificação Científica

FOS: Ciências exactas e naturais > Matemática

Outras Informações

ID Authenticus: P-003-SZQ

DOI: 10.1007/978-3-540-85861-4_22

Abstract (EN): This work presents a method of knowledge discovery in data obtained from Molecular Dynamics Protein Unfolding Simulations. The data under study was obtained from simulations of the unfolding process of the protein Transthyretin (TTR), responsible for amyloid diseases such as Familial Amyloid Polyneuropathy (FAP). Protein unfolding and misfolding are at the source of many amyloidogenic diseases. Thus, the molecular characterization of protein unfolding processes through experimental and simulation methods may be essential in the development of effective treatments. Here, we analyzed the distance variation of each of the 127 amino acids C. (alpha carbon) atoms of TTR to the centre of mass of the protein, along 10 different unfolding simulations - five simulations of WT-TTR and five simulations of L55P-TTR, a highly amyloidogenic TTR variant. Using data mining techniques, and considering all the information of the 10 runs, we identified several clusters of amino acids. For each cluster we selected the representative element and identified events which were used as features. With Association Rules we found patterns that characterize the type of TTR variant under study. These results may help discriminate between amyloidogenic and non-amyloidogenic behaviour among different TTR variants and contribute to the understanding of the molecular mechanisms of FAP.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 9