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Glutaraldehyde: behavior in aqueous solution, reaction with proteins, and application to enzyme crosslinking

    Isabelle Migneault

    Université de Montréal, Montréal, Canada

    ,
    Catherine Dartiguenave

    Université de Montréal, Montréal, Canada

    ,
    Michel J. Bertrand

    Université de Montréal, Montréal, Canada

    &
    Karen C. Waldron

    *Address correspondence to: Karen C. Waldron, Department of Chemistry, Université de Montréal, C.P. 6128, Succ. Centre-ville, Montréal, Canada, H3C 3J7. e-mail:

    E-mail Address: karen.waldron@umontreal.ca

    Université de Montréal, Montréal, Canada

    Published Online:https://doi.org/10.2144/04375RV01

    Glutaraldehyde possesses unique characteristics that render it one of the most effective protein crosslinking reagents. It can be present in at least 13 different forms depending on solution conditions such as pH, concentration, temperature, etc. Substantial literature is found concerning the use of glutaraldehyde for protein immobilization, yet there is no agreement about the main reactive species that participates in the crosslinking process because monomeric and polymeric forms are in equilibrium. Glutaraldehyde may react with proteins by several means such as aldol condensation or Michael-type addition, and we show here 8 different reactions for various aqueous forms of this reagent. As a result of these discrepancies and the unique characteristics of each enzyme, crosslinking procedures using glutaraldehyde are largely developed through empirical observation. The choice of the enzyme-glutaraldehyde ratio, as well as their final concentration, is critical because insolubilization of the enzyme must result in minimal distortion of its structure in order to retain catalytic activity. The purpose of this paper is to give an overview of glutaraldehyde as a crosslinking reagent by describing its structure and chemical properties in aqueous solution in an attempt to explain its high reactivity toward proteins, particularly as applied to the production of insoluble enzymes.

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