Asymmetric Photocross-linking Pattern of Restriction EndonucleaseEcoRII to the DNA Recognition Sequence

• Published in: The Journal of biological chemistry Vol. 277; no. 16; pp. 14288 - 14293
• Main Authors: Mücke, Merlind, Pingoud, Vera, Grelle, Gerlinde, Kraft, Regine, Krüger, Detlev H., Reuter, Monika
• Format: Journal Article
• Language: English
• Published: Elsevier Inc 19.04.2002; American Society for Biochemistry and Molecular Biology
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M109311200

The EcoRII homodimer engages two of its recognition sequences (5′-CCWGG) simultaneously and is therefore a type IIE restriction endonuclease. To identify the amino acids ofEcoRII that interact specifically with the recognition sequence, we photocross-linked EcoRII with oligonucleotide substrates that contained only one recognition sequence forEcoRII. In this recognition sequence, we substituted either 5-iododeoxycytidine for each C or 5-iododeoxyuridine for A, G, or T. These iodo-pyrimidine bases were excited using a UV laser to result in covalent cross-linking products. The yield of EcoRII photocross-linked to the 5′-C of the 5′-CCAGG strand of the recognition sequence was 45%. However, we could not photocross-linkEcoRII to the 5′-C of the 5′-CCTGG strand. Thus, the contact of EcoRII to the bases of the recognition sequence appears to be asymmetric, unlike that expected for most type II restriction endonucleases. Tryptic digestion of free and of cross-linked EcoRII, followed by high performance liquid chromatography (HPLC) separation of the individual peptides and Edman degradation, identified amino acids 25–49 of EcoRII as the cross-linking peptide. Mutational analysis of the electron-rich amino acids His36 and Tyr41 of this peptide indicates that Tyr41 is the amino acid involved in the cross-link and that it therefore contributes to specific DNA recognition by EcoRII.