Mechanism of photochemical internalization

• Grant number: 13/16532-1
• Support Opportunities: Scholarships in Brazil - Doctorate (Direct)
• Start date: November 01, 2013
• End date: February 28, 2017
• Field of knowledge: Biological Sciences - Biophysics - Radiology and Photobiology
• Principal Investigator: Mauricio da Silva Baptista
• Grantee: Tayana Mazin Tsubone
• Host Institution: Instituto de Química (IQ). Universidade de São Paulo (USP). São Paulo , SP, Brazil
• Associated research grant: 12/50680-5 - Photosensitization in life sciences, AP.TEM

Abstract

Photochemical Internalization (PCI) can revolutionize the drug or biomolecules delivery inside eukaryotic cells. This concept is grounded on the use of photosensitizers (PS), which localize mainly in endocytic vesicles membrane, it is photo-damaged and enable the release of lumem endocytic vesicles membrane into citosol. PCI has been risen the protocols efficiency in the cancer therapy. Moreover, PCI has shown the capability to improve active biomolecules delivery (gene, proteins) into intracellular environment. However, even PCI has this potential, the real application in clinical practice is very limited (some groups distributed around the world are testing this strategy). This occurs probably because there are little mechanism known about cellular processes involved in PCI, resulting in only empirical protocols. Therefore, deepening studies of PCI mechanisms will be of great value. In the beginning of graduate, the candidate for this project studied interaction between porphyrins and membranes and its relation to the photoactivity using various photophysical and biophysical techniques. The candidate featured amphiphilic molecules that interact strongly with cellular membrane thereby increasing the photodynamic activity. These studies provided the basis for proposing a project focusing on understanding the mechanisms of PCI, since it know that it is required a strong interaction and accumulation of PS in the plasma membrane in order to the drug delivery be satisfactory in PCI. Two photosensitizers, in the series studied by the applicant, showed equally efficient binding and damage to membranes. Therefore, in this project we intend to increase the knowledge about mechanism envolved in PCI and for this we will use these two oppositely charged photosensitizers TPPS2a e Cis-DiMPyP, as well as a polymer photosensitizer (PPIX covalently bound to poly-L-lysine) recently developed in the laboratory. Furthermore, internalization of antitumor drug (doxorubicin) and polymer dextran labeled with fluorescent probes (FITC-dextran 4 and 250kDa) in two cell lines (HeLa and HaCaT) will be our study models. We intend to evaluate: i) the effect of charged porphyrins (positively and negatively); ii) the difference between the release kinetics of substrates which are already in lysosomes compared with those which are provided in the extracellular environment endocytosed; iii) the effect of endocytosis inhibition by Caveolae, removing cholesterol from cytoplasmic membrane; iv) the effect of the suspended autophagic flow in PCI; v) relationship between the induction mechanisms of programmed cell death (apoptosis and autophagy) and PCI. The expected result of this work a deeper understanding of the mechanisms involved in PCI and perhaps the development of molecules that are more efficient. (AU)

Scientific publications

(5)

(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)

TSUBONE, TAYANA MAZIN; MARTINS, WALESKA KERLLEN; BAPTISTA, MAURICIO S.. Identifying Specific Subcellular Organelle Damage by Photosensitized Oxidations. YALE JOURNAL OF BIOLOGY AND MEDICINE, v. 92, n. 3, p. 413-422, SEP 2019. (13/16532-1, 13/07937-8)

TSUBONE, TAYANA MAZIN; ZHANG, ZHENG; GOYAL, RITU; SANTACRUZ, CAROLINA; MARTINS, WALESKA KERLLEN; KOHN, JOACHIM; BAPTISTA, MAURICIO S.. Porphyrin-Loaded TyroSpheres for the Intracellular Delivery of Drugs and Photoinduced Oxidant Species. MOLECULAR PHARMACEUTICS, v. 17, n. 8, p. 2911-2924, AUG 3 2020. (13/16532-1, 13/07937-8)

TASSO, THIAGO T.; TSUBONE, TAYANA M.; BAPTISTA, MAURICIO S.; MATTIAZZI, LIA M.; ACUNHA, THIAGO V.; IGLESIAS, BERNARDO A.. Isomeric effect on the properties of tetraplatinated porphyrins showing optimized phototoxicity for photodynamic therapy. DALTON TRANSACTIONS, v. 46, n. 33, p. 11037-11045, SEP 7 2017. (16/15916-9, 13/07937-8, 12/50680-5, 13/16532-1)

TSUBONE, TAYANA MAZIN; MARTINS, WALESKA KERLLEN; PAVANI, CHRISTIANE; JUNQUEIRA, HELENA COUTO; ITRI, ROSANGELA; BAPTISTA, MAURICIO S.. Enhanced efficiency of cell death by lysosome-specific photodamage. SCIENTIFIC REPORTS, v. 7, JUL 27 2017. (12/10049-4, 13/07937-8, 12/50680-5, 13/16532-1)

BACELLAR, ISABEL O. L.; TSUBONE, TAYANA M.; PAVANI, CHRISTIANE; BAPTISTA, MAURICIO S.. Photodynamic Efficiency: From Molecular Photochemistry to Cell Death. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v. 16, n. 9, p. 20523-20559, SEP 2015. (13/11640-0, 13/07937-8, 13/16532-1)

Academic Publications

(References retrieved automatically from State of São Paulo Research Institutions)

TSUBONE, Tayana Mazin. Specificity and bioavailability of photosensitizers: In the search of an optimized photosensitizer for photodynamic therapy. 2017. Doctoral Thesis - Universidade de São Paulo (USP). Conjunto das Químicas (IQ e FCF) (CQ/DBDCQ) São Paulo.