Research Groups
Proteomics
Group Leader
Research Interests and DescriptionGroup Members
Alessandro Vindigni
International Centre for Genetic Engineering and BiotechnologyPadriciano 99
34012 Trieste, Italy
E-mail: vindigni@icgeb.org
Office tel: +39-040-3757369
Lab tel: +39-040-3757326
Office fax: +39-040-226555
Education
University of Padua, Padua, Italy, Degree in Chemistry, 1992University of Padua, Padua, Italy, PhD in Biochemistry and Molecular Biophysics, 1995
Career History
Since 2002, Group Leader of the Proteomics Laboratory, International Centre for Genetic Engineering and Biotechnology (ICGEB), Trieste, Italy.1999-2002, Staff Scientist, Molecular Biology Group, ICGEB, Trieste, Italy.
1995-1999, Postdoctoral fellow, Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, MO, USA.
1994-1995, PhD student, Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, MO, USA.
1992-1994, PhD student, CRIBI Biotechnology Centre, University of Padua, Padua, Italy.
1991-1992, Undergraduate student, CRIBI Biotechnology Centre, University of Padua, Italy.
1990, ERASMUS exchange student, Chemistry Dept., University of Newcastle upon Tyne, England.
Honors
1996-1998, American Heart Association Postdoctoral Fellowship.
1995-1996, W.M. Keck Fellowship, Washington University School of Medicine.
Teaching Activity
2009, co-organizer of the ICGEB Workshop on “Proteomic Characterization of Macromolecular Complexes Involved in DNA Metabolism”, to be held in Trieste, Italy.2008, co-organizer of the ICGEB Theoretical and Practical Course entitled “Proteomic Approaches in Molecular Biology: Theory and Practice”, Buenos Aires, Argentina.
Since 2003, external Professor of Proteomics, Faculty of Medicine, University of Trieste, Italy.
Since 2003, DNA repair course for the 1st year PhD candidates of the Open University/Scuola Normale Superiore at ICGEB, Trieste, Italy.
Scientific Activity
The Group is interested in the characterization of the enzymatic activity and function of enzymes involved in DNA damage and repair. In particular, we now focus on RecQ helicases. A combination of biochemical, proteomic, and structural approaches is used to shed light on the role of these enzymes in the maintenance of genome integrity. Moreover, we are also interested in DNA non-homologous end-joining (NHEJ), one of the two major mechanisms of double strand break repair in cells.Selected publications
Kusumoto, R., Dawut, L., Marchetti, C., Wan Lee, J., Vindigni, A., Ramsden, D., Bohr, V.A. 2008. Werner protein cooperates with the XRCC4-DNA ligase IV complex in end-processing. Biochemistry 47, 7548-7556Milli, A., Cecconi, D., Campostrini, N., Timperio, A.M., Zolla, L., Righetti, S.C., Zunino, F., Perego, P., Benedetti, V., Gatti, L., Odreman, F., Vindigni, A., Rigetti, P.G. 2008. A proteomic approach for evaluating the cell response to a novel histone deacetylase inhibitor in colon cancer cells. Biochim. Biophys. Acta, epub ahead of print
Popuri, V., Bachrati, C.Z., Muzzolini, L., Mosedale, G., Costantini, S., Giacomini, E., Hickson, I.D., Vindigni, A. 2008. The human RecQ helicases, BLM and RECQ1, display distinct DNA substrate specificities. J. Biol. Chem. 283, 17766-17776
Amiard, S., Doudeau, M., Pinte, S., Poulet, A., Lenain, C., Faivre-Moskalenko, C., Angelov, D., Hug, N., Vindigni, A., Bouvet, P., Paoletti, J., Gilson, E., Giraud-Panis, MJ. 2007. A topological mechanism for TRF2-enhanced strand invasion. Nat. Struct. Mol. Biol. 14,147-154
Costantini, S., Woodbine, L., Andreoli, L., Jeggo, P.A., Vindigni, A. 2007. Interaction of the Ku heterodimer with the DNA ligase IV/Xrcc4 complex and its regulation by DNA-PK. DNA Repair 6, 712-722
Muzzolini, L., Beuron, F., Patwardhan, A., Popuri, V., Cui, S., Niccolini, B., Rappas, M., Freemont, P.S., Vindigni, A. 2007. Different Quaternary Structures of Human RECQ1 Are Associated with its Dual Enzymatic Activity. PLoS Biology, 5, e(20).
Nijnik, A., Woodbine, L., Marchetti, C., Dawson, S., Lambe, T., Liu, C., Rodrigues, N.P., Crockford, T.L., Cabuy, E., Vindigni, A., Enver, T., Bell, J.I., Slijepcevic, P., Goodnow, C.C., Jeggo, P.A., Cornall, R.J. 2007. DNA repair is limiting for haematopoietic stem cells during ageing. Nature 447, 686-690
Vindigni, A. 2007. Biochemical, biophysical, and proteomic approaches to study DNA helicases. Mol. Biosyst. 3, 266-274
Pozzi Mucelli, S., Odreman, F., Lujardo Gonzales, M., Gerardi, E., Stanta, G., Vindigni, A. 2006. Proteomic studies on the white matter of human brain. J. Chromatogr. B 833, 80-90
Odreman, F., Vindigni, M., Lujardo Gonzales, M., Niccolini, B., Candiano, G., Zanotti, B., Skrap, M., Pizzolitto, S., Stanta, G., Vindigni, A. 2005. Proteomic studies on low- and high-grade human brain astrocytomas. J. Proteome Res. 4, 698-708
Wu, L., Chan, K.L., Ralf, C., Bernstein, D.A., Garcia, P.L., Bohr, V.A., Vindigni, A., Janscak, P., Keck, J.L., Hickson, I.D. 2005. The HRDC domain of BLM is required for the recognition, processing and dissolution of double Holliday junctions. EMBO J. 24, 2679-2687
Arosio, D., Costantini, S., Kong, Y., Vindigni, A. 2004. Fluorescence anisotropy studies of the Ku-DNA interaction: anion and cation effects. J. Biol. Chem. 279, 42826-42835
Cui, S., Arosio, D., Doherty, K.M., Brosh, R.M. Jr., Falaschi, A., Vindigni, A. 2004. Analysis of the unwinding activity of the dimeric RECQ1 helicase in the presence of human replication protein A. Nucleic Acids Res. 32, 2158-2170
Cui, S., Klima, R., Ochem, A., Arosio, D., Falaschi, A., Vindigni, A. 2003. Characterization of the DNA-unwinding activity of human RECQ1, a helicase specifically stimulated by human replication protein A. J. Biol. Chem. 278, 1424-1432
Arosio, D., Cui, S., Ortega, C., Chovanec, M., Di Marco, S., Baldini, G., Falaschi, A., Vindigni, A. 2002. Studies on the mode of Ku interaction with DNA. J. Biol. Chem. 277, 9741-9748
Vindigni, A. 1999. Energetic Dissection of Specificity in Serine Proteases. Combinatorial Chemistry and High Throughput Screening 2, 125-139.
Ido, Y., Vindigni, A., Chang, K., Di Cera, E., Williamson, J.R. 1997. C-peptide Prevents Vascular and Neural Dysfunction in Diabetic Rats. Science 277, 563-566
Vindigni, A., Dang, Q.D., Di Cera, E. 1997. Site-specific dissection of substrate recognition by thrombin. Nature Biotechnol. 15, 891-895



















