The broad recognition specificity exhibited by integrin α_Mβ₂ (Mac-1, CD11b/CD18) has allowed this adhesion receptor to play innumerable roles in leukocyte biology, yet we know little about how and why α_Mβ₂ binds its multiple ligands. Within α_Mβ₂, the α_MI-domain is responsible for integrin’s multiligand binding properties. To identify its recognition motif, we screened peptide libraries spanning sequences of many known protein ligands for α_MI-domain binding and also selected the α_M I-domain recognition sequences by phage display. Analyses of >1400 binding and nonbinding peptides derived from peptide libraries showed that a key feature of the α_MI-domain recognition motif is a small core consisting of basic amino acids flanked by hydrophobic residues. Furthermore, the peptides selected by phage display conformed to a similar pattern. Identification of the recognition motif allowed the construction of an algorithm that reliably predicts the α_MI-domain binding sites in the α_Mβ₂ ligands. The recognition specificity of the α_MI-domain resembles that of some chaperones, which allows it to bind segments exposed in unfolded proteins. The disclosure of the α_Mβ₂ binding preferences allowed the prediction that cationic host defense peptides, which are strikingly enriched in the α_MI-domain recognition motifs, represent a new class of α_Mβ₂ ligands. This prediction has been tested by examining the interaction of α_Mβ₂ with the human cathelicidin peptide LL-37. LL-37 induced a potent α_Mβ₂-dependent cell migratory response and caused activation of α_Mβ₂ on neutrophils. The newly revealed recognition specificity of α_Mβ₂ toward unfolded protein segments and cationic proteins and peptides suggests that α_Mβ₂ may serve as a previously proposed “alarmin” receptor with important roles in innate host defense.