Proton-coupled electron transfer in the Escherichia coli ribonucleotide reductase

Ribonucleotide reductases (RNRs) comprise a biologically indispensable enzyme class which converts the four common nucleotides to their corresponding deoxynucleotides via a thiyl radical hydrogen abstraction mechanism. As this is the only cellular pathway for production of the monomeric precursors required for DNA synthesis, the regulation of RNR is crucial to controlling the cell cycle by the availability of substrate pools for DNA replication. The class I RNR from E. coli is composed of two subunits; the R1 subunit contains the active site for nucleotide reduction, as well as the allosteric effector binding sites, and the R2 subunit contains the stable Y122·-diiron cofactor. Based on the conserved mode of action of the class II and mII RNRs, Y122· is proposed to oxidize C439 in R1 to the active thiyl radical species through a long-range radical transfer pathway involving several conserved aromatic residues (in R2: Y122, W48, Y356; in RI:Y731, Y730), which is unprecedented for its length (35 [angstroms]). Although this model is supported by in vitro and in vivo mutagenesis studies as well as sequence conservation, direct evidence for radical intermediates along this pathway has been masked by conformational gating. We have initiated R1 nucleotide reduction in the absence of R2, using a photoactive derivative of the R2 C-terminal peptide, containing the essential Y356. This peptide is capable of generating a tyrosyl radical upon photolysis and provides a specific entry point into the radical initiation pathway of R1. We now report that catalytic turnover in R1 may be triggered in the absence of R2 by the photogeneration of a conserved aromatic amino acid radical located within a synthetic 21-mer peptide derived from the R2 C-terminus.

Department dc:contributor.department

Massachusetts Institute of Technology. Dept. of Chemistry.

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2004

Author dc:creator

• Chang, Michelle C. Y. (Michelle Chia-yu), 1977-

Advisor dc:contributor.advisor

• Daniel G. Nocera.

• Chemistry.

Statement dc:rights

• M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/30067

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/30067