2015, Number 2
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Rev Cubana Farm 2015; 49 (2)
Cyclotides, circular proteins produced by plants with pharmacological potential
Contreras PE, Díaz CA, Taron DA
Language: Spanish
References: 21
Page: 384-393
PDF size: 114.53 Kb.
ABSTRACT
The ciclotydes are circular proteins of 28 to 37 aminoacid that have a unique and strong cyclic structural motif which confers stability and relevant biological
activities. In this study we searched in data bases
EBSCOHOST, Science Direct, Pubmed and
ACS publication to identify relevant studies considering inclusion criteria such as full-text articles in English, original experimental research related to the use of cyclotides in drug design. The biological activities of the cyclotides have been reported as insecticide, uterotonic, antimicrobial, antiHIV, anticancer,
hemolytic, neurotensin antagonist and inhibitor of trypsin which can be used as basis for the development of new drugs that can be applied to the treatment of
various diseases.
REFERENCES
Park S, Stromstedt AA, Goransson U. Cyclotide structure-activity relationships: qualitative and quantitative approaches linking cytotoxic and anthelmintic activity to the clustering of physicochemical forces. PloS one. 2014;9(3):e91430.
Hashempour H, Koehbach J, Daly NL, Ghassempour A, Gruber CW. Characterizing circular peptides in mixtures: sequence fragment assembly of cyclotides from a violet plant by MALDI-TOF/TOF mass spectrometry. Amino acids. 2013;44(2):581-95.
Wang CK, Clark RJ, Harvey PJ, Rosengren KJ, Cemazar M, Craik DJ. The role of conserved Glu residue on cyclotide stability and activity: a structural and functional study of kalata B12, a naturally occurring Glu to Asp mutant. Biochemistry. 2011;50(19):4077-86.
Garcia AE, Camarero JA. Biological activities of natural and engineered cyclotides, a novel molecular scaffold for peptide-based therapeutics. Current molecular pharmacology. 2010;3(3):153-63.
Poth AG, Colgrave ML, Philip R, Kerenga B, Daly NL, Anderson MA, et al. Discovery of cyclotides in the fabaceae plant family provides new insights into the cyclization, evolution, and distribution of circular proteins. ACS chemical biology. 2011;6(4):345-55.
Craik DJ, Conibear AC. The chemistry of cyclotides. The Journal of organic chemistry. 2011;76(12):4805-17.
Ireland DC, Clark RJ, Daly NL, Craik DJ. Isolation, sequencing, and structure-activity relationships of cyclotides. Journal of natural products. 2010;73(9):1610-22.
Gran L. Oxytocic principles of Oldenlandia affinis. Lloydia. 1973;36(2):174-8. Epub 1973/06/01.
Goransson U, Burman R, Gunasekera S, Stromstedt AA, Rosengren KJ. Circular proteins from plants and fungi. The Journal of biological chemistry. 2012;287(32):27001-6.
Burman R, Gruber CW, Rizzardi K, Herrmann A, Craik DJ, Gupta MP, et al. Cyclotide proteins and precursors from the genus Gloeospermum: filling a blank spot in the cyclotide map of Violaceae. Phytochemistry. 2010;71(1):13-20.
Henriques ST, Huang YH, Rosengren KJ, Franquelim HG, Carvalho FA, Johnson A, et al. Decoding the membrane activity of the cyclotide kalata B1: the importance of phosphatidylethanolamine phospholipids and lipid organization on hemolytic and anti-HIV activities. The Journal of biological chemistry. 2011;286(27):24231-41.
Pranting M, Loov C, Burman R, Goransson U, Andersson DI. The cyclotide cycloviolacin O2 from Viola odorata has potent bactericidal activity against Gramnegative bacteria. The Journal of antimicrobial chemotherapy. 2010;65(9):1964-71.
Sando L, Henriques ST, Foley F, Simonsen SM, Daly NL, Hall KN, et al. A Synthetic mirror image of kalata B1 reveals that cyclotide activity is independent of a protein receptor. Chembiochem. 2011;12(16):2456-62.
Tang J, Wang CK, Pan X, Yan H, Zeng G, Xu W, et al. Isolation and characterization of cytotoxic cyclotides from Viola tricolor. Peptides. 2010;31(8):1434-40.
Gerlach SL, Burman R, Bohlin L, Mondal D, Goransson U. Isolation, characterization, and bioactivity of cyclotides from the Micronesian plant Psychotria leptothyrsa. Journal of natural products. 2010;73(7):1207-13.
Yeshak MY, Burman R, Asres K, Goransson U. Cyclotides from an extreme habitat: characterization of cyclic peptides from Viola abyssinica of the Ethiopian highlands. Journal of natural products. 2011;74(4):727-31.
Craik DJ, Mylne JS, Daly NL. Cyclotides: macrocyclic peptides with applications in drug design and agriculture. Cellular and molecular life sciences. CMLS. 2010;67(1):9-16.
Craik DJ. Host-defense activities of cyclotides. Toxins. 2012;4(2):139-56.
Nawae W, Hannongbua S, Ruengjitchatchawalya M. Defining the membrane disruption mechanism of kalata B1 via coarse-grained molecular dynamics simulations. Scientific reports. 2014;4:3933.
Tam JP, Lu YA, Yang JL, Chiu KW. An unusual structural motif of antimicrobial peptides containing end-to-end macrocycle and cystine-knot disulfides. Proceedings of the National Academy of Sciences of the United States of America. 1999;96(16):8913-8.
Craik DJ. Plant cyclotides: circular, knotted peptide toxins. Toxicon. 2001;39(12):1809-13.