Our understanding of the rules relating sequence to structure in antibodies has led to the development of accurate knowledge-based procedures for antibody modeling. Information gained from the analysis of antibody structures has been successfully exploited to engineer antibody-like molecules endowed with prescribed properties, such as increased stability or different specificity, many of which have a broad spectrum of applications both in therapy and in research. Here we describe a knowledge-based procedure for the prediction of the antibody-variable domains, based on the canonical structures method for the antigen-binding site, and discuss its expected accuracy and limitations. The rational design of antibody-based molecules is illustrated using as an example one of the most widely employed modifications of antibody structures: the humanization of animal-derived antibodies to reduce their immunogenicity for serotherapy in humans. (C) 2000 Academic Press.

Antibody modeling: Implications for engineering and design

Morea V;
2000

Abstract

Our understanding of the rules relating sequence to structure in antibodies has led to the development of accurate knowledge-based procedures for antibody modeling. Information gained from the analysis of antibody structures has been successfully exploited to engineer antibody-like molecules endowed with prescribed properties, such as increased stability or different specificity, many of which have a broad spectrum of applications both in therapy and in research. Here we describe a knowledge-based procedure for the prediction of the antibody-variable domains, based on the canonical structures method for the antigen-binding site, and discuss its expected accuracy and limitations. The rational design of antibody-based molecules is illustrated using as an example one of the most widely employed modifications of antibody structures: the humanization of animal-derived antibodies to reduce their immunogenicity for serotherapy in humans. (C) 2000 Academic Press.
2000
antibody modeling
canonical structures
CDRs
loop grafting
protein engineering
RESHAPING HUMAN-ANTIBODIES
MONOCLONAL-ANTIBODY
HYPERVARIABLE REGION
PROTEIN STRUCTURES
BETA-HAIRPINS
3-DIMENSIONAL STRUCTURE
CANONICAL STRUCTURES
ANTIGEN INTERACTIONS
SEQUENCE ALIGNMENT
GLOBULAR-PROTEINS
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/198502
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