The long-term objective of this proposal is to develop synthetic methodology that can be used to gain deep insight into the biological properties of porphyrinic molecules and can be exploited in diagnostic and therapeutic applications. The term """"""""porphyrinic"""""""" encompasses tetrapyrrole macrocycles that are fully unsaturated (porphyrins) or partially reduced (hydroporphyrins; such as chlorins or bacteriochlorins). The specific objective is to develop powerful routes for the synthesis of water-soluble, bioconjugatable porphyrins and hydroporphyrins. Hydroporphyrins absorb strongly in the red/near-IR spectral region, an ideal wavelength of light for deep penetration of cells and tissues. Such compounds are anticipated to have widespread biological applications where active targeting with a red/near-IR label is required, yet hydroporphyrins with the requisite molecular design features have not been available synthetically. The hydroporphyrins will bear one conjugatable handle, one or more water-solubilizing groups, structural features to prevent dehydrogenation and suppress oxidation, and tunable photochemistry via alteration of the centrally coordinated metal. Strategies for the rational synthesis of bacteriochlorins will be developed, including the derivatization of porphyrins, the derivatization of chlorins, and synthesis de novo. In the development of new synthetic routes, attention will be paid to issues of simplicity, scope, and scale, thereby enabling widespread utilization by a broad range of scientists from diverse fields. New molecular motifs will be investigated for achieving water solubility, a key requirement for use in biomolecule labeling studies. The basic science for the use of hydroporphyrin-biomolecule conjugates will be addressed by first characterizing the intrinsic properties of the hydroporphyrins, then characterizing the loading, non-covalent binding, aggregation, photostability, and brightness of hydroporphyrin-antibody conjugates. This work will open the door to applications such as multicolor/multiparameter labeling of cells and intracellular components, and provide a sound basis for the design and development of next-generation molecules for use in diverse therapeutic applications where active-targeting strategies are sought.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM036238-20
Application #
7155556
Study Section
Metallobiochemistry Study Section (BMT)
Program Officer
Fabian, Miles
Project Start
1986-12-01
Project End
2007-11-30
Budget Start
2006-12-01
Budget End
2007-11-30
Support Year
20
Fiscal Year
2007
Total Cost
$277,978
Indirect Cost
Name
North Carolina State University Raleigh
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
042092122
City
Raleigh
State
NC
Country
United States
Zip Code
27695
Lindsey, Jonathan S (2015) De novo synthesis of gem-dialkyl chlorophyll analogues for probing and emulating our green world. Chem Rev 115:6534-620
Huang, Liyi; Huang, Ying-Ying; Mroz, Pawel et al. (2010) Stable synthetic cationic bacteriochlorins as selective antimicrobial photosensitizers. Antimicrob Agents Chemother 54:3834-41
Mroz, Pawel; Huang, Ying-Ying; Szokalska, Angelika et al. (2010) Stable synthetic bacteriochlorins overcome the resistance of melanoma to photodynamic therapy. FASEB J 24:3160-70
Huang, Ying-Ying; Mroz, Pawel; Zhiyentayev, Timur et al. (2010) In vitro photodynamic therapy and quantitative structure-activity relationship studies with stable synthetic near-infrared-absorbing bacteriochlorin photosensitizers. J Med Chem 53:4018-27
Mroz, Pawel; Bhaumik, Jayeeta; Dogutan, Dilek K et al. (2009) Imidazole metalloporphyrins as photosensitizers for photodynamic therapy: role of molecular charge, central metal and hydroxyl radical production. Cancer Lett 282:63-76
Kee, Hooi Ling; Bhaumik, Jayeeta; Diers, James R et al. (2008) Photophysical Characterization of Imidazolium-Substituted Pd(II), In(III), and Zn(II) Porphyrins as Photosensitizers for Photodynamic Therapy. J Photochem Photobiol A Chem 200:346-355
Borbas, K Eszter; Ruzie, Christian; Lindsey, Jonathan S (2008) Swallowtail bacteriochlorins. Lipophilic absorbers for the near-infrared. Org Lett 10:1931-4
Muresan, Ana Z; Lindsey, Jonathan S (2008) Design and synthesis of water-soluble bioconjugatable trans-AB-porphyrins. Tetrahedron 64:11440-11448
Dogutan, Dilek Kiper; Lindsey, Jonathan S (2008) Investigation of the scope of a new route to ABCD-bilanes and ABCD-porphyrins. J Org Chem 73:6728-42
Borbas, K Eszter; Kee, Hooi Ling; Holten, Dewey et al. (2008) A compact water-soluble porphyrin bearing an iodoacetamido bioconjugatable site. Org Biomol Chem 6:187-94

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