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Immunity proteins and their specificity for endonuclease colicins: telling right from wrong in protein–protein recognition
Author(s) -
Kleanthous Colin,
Hemmings Andrew M.,
Moore Geoffrey R.,
James Richard
Publication year - 1998
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1046/j.1365-2958.1998.00811.x
Subject(s) - colicin , biology , immunity , dna binding protein , protein superfamily , genetics , microbiology and biotechnology , biochemistry , immune system , escherichia coli , transcription factor , gene
Immunity proteins inhibit colicins, protein toxins released by bacteria during times of environmental stress, by binding and inactivating their cytotoxic domains. This protects the producing organism as it attempts to kill off competing bacteria. The cytotoxic domains of related colicins share a high degree of sequence identity, as do their corresponding immunity proteins, yet specificity and affinity are also high, with little non‐cognate biological cross‐protection evident under physiological conditions. We review recent work on DNase‐specific immunity proteins, which shows that, although both cognate and non‐cognate proteins can bind a single toxin, their affinities can differ by as much as 12 orders of magnitude. We have termed this mode of binding dual recognition, because the DNase‐binding surface of an immunity protein is made up of two components, one conserved and the other variable. The strength of the binding interaction is dominated by the conserved residues, while neighbouring variable residues control specificity. Similar dual recognition systems may exist in other biological contexts, particularly where a protein must discriminate the right binding partner from numerous, structurally homologous alternatives.