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A new addition to the structural bioinformatics toolbox: 3D models of short bioactive peptides from multiple sequences using feedback restrained molecular dynamics (FRMD)

  1. Author:
    Cachau, R. E.
    Gonzalez-Sapienza, G.
    Burt, S. K.
    Ventura, O. N.
  2. Author Address

    SAIC Frederick Inc, Natl Canc Inst, Adv Biomed Comp Ctr, Ft Detrick, MD 21702 USA SAIC Frederick Inc, Natl Canc Inst, Adv Biomed Comp Ctr, Ft Detrick, MD 21702 USA Univ Republica, Fac Quim, Catedra Inmunol, Montevideo 11600, Uruguay UDELAR, Fac Quim, CCPG, DEQUIFIM, Montevideo 11800, Uruguay Cachau RE SAIC Frederick Inc, Natl Canc Inst, Adv Biomed Comp Ctr, Ft Detrick, MD 21702 USA
    1. Year: 2003
  1. Journal: Cellular and Molecular Biology
    1. 49
    2. 6
    3. Pages: 973-983
  2. Type of Article: Article
  1. Abstract:

    Modem molecular biology techniques allow the use of new approaches for the 3D mapping of 1D information. Molecular biology techniques are capable of producing large amounts of 1D information (sequences) from a number of different sources (phage displays, ESTs etc.). In this work, we present a technique that takes advantage of large sets of 1D information and increasingly available computer power to create 3D models. For the purpose of validation the technique is first applied to the modeling of an erythropoietin analog of known 3D structure from 1D information only. The technique is then used to model the immunoreactive region of echinococcus granulosus AgB based on phage raised mimotopes for which there is no previous structural information. The technique here presented is of general application to similar problems where 1D information is available and structure activity relationships (SAR) is needed.

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