Document Type
Article
Language
eng
Format of Original
10 p.
Publication Date
1-2005
Publisher
Springer
Source Publication
Journal of Biological Inorganic Chemistry
Source ISSN
0949-8257
Original Item ID
doi: 10.1007/s00775-004-0611-7
Abstract
EPR spectra were recorded for methionine aminopeptidase from Escherichia coli (EcMetAP-I) samples (~2.5 mM) to which one and two equivalents of Mn(II) were added (the latter is referred to as [MnMn(EcMetAP-I)]). The spectra for each sample were indistinguishable except that the spectrum of [MnMn(EcMetAP-I)] was twice as intense. The EPR spectrum of [MnMn(EcMetAP-I)] exhibited the characteristic six-line g≈2 EPR signal of mononuclear Mn(II) with A av(55Mn)=9.3 mT (93 G) and exhibited Curie-law temperature dependence. This signal is typical of Mn(II) in a ligand sphere comprising oxygen and/or nitrogen atoms. Other features in the spectrum were observed only as the temperature was raised from that of liquid helium. The temperature dependences of these features are consistent with their assignment to excited state transitions in the S=1, 2 ... 5 non-Kramer’s doublets, due to two antiferromagnetically coupled Mn(II) ions with an S=0 ground state. This assignment is supported by the observation of a characteristic 4.5 mT hyperfine pattern, and by the presence of signals in the parallel mode consistent with a non-Kramer’s spin ladder. Upon the addition of the anti-angiogenesis agent fumagillin to [MnMn(EcMetAP-I)], very small changes were observed in the EPR spectrum. MALDI-TOF mass spectrometry indicated that fumagillin was, however, covalently coordinated to EcMetAP-I. Therefore, the inhibitory action of this anti-angiogenesis agent on EcMetAP-I appears to involve covalent binding to a polypeptide component at or near the active site rather than direct binding to the metal ions.
Recommended Citation
D'Souza, Ventris M.; Brown, Robert S.; Bennett, Brian; and Holz, Richard C., "Characterization of the Active Site and Insight into the Binding Mode of the Anti-angiogenesis Agent Fumagillin to the Manganese(II)-Loaded Methionyl Aminopeptidase from Escherichia coli" (2005). Physics Faculty Research and Publications. 81.
https://epublications.marquette.edu/physics_fac/81
Comments
Accepted version. Journal of Biological Inorganic Chemistry, Vol. 10, No. 1 (January 2005): 41-50. DOI. © 2005 Springer Nature Switzerland AG. Part of Springer Nature. Used with permission.
Brian Bennett was affiliated with the Medical College of Wisconsin at the time of publication.
Richard Holz was affiliated with Utah State University at the time of publication.
Shareable Link. Provided by the Springer Nature SharedIt content-sharing initiative.