LC-MS/MS identification and cytotoxic assessment of jaspamide and its congeners from the sponge Jaspis diastra

被引:2
作者
Ramanjooloo, Avin [1 ,2 ]
Kamel, Mahmoud [3 ]
Adeyemi, Samson A. A. [4 ]
Ubanako, Philemon [4 ]
Baudot, Bertrand [3 ]
Thakoor, Asho D. D. [1 ]
Choonara, Yahya E. E.
Bhaw-Luximon, Archana [1 ]
机构
[1] Univ Mauritius, Ctr Biomed & Biomat Res, Biomat Drug Delivery & Nanotechnol Unit, MSIRI Bldg, Moka, Mauritius
[2] Mauritius Oceanog Inst, Ave Anchois, Albion, Mauritius
[3] Socota Phoenicia, Quantilab, Biopk Mauritius, Sayed Hossen Rd, Vacoas Phoenix 73408, Mauritius
[4] Univ Witwatersrand, Johannesburg, South Africa
关键词
MARINE SPONGE; ACTIN POLYMERIZATION; BIOACTIVE PEPTIDES; ETHYL-ACETATE; JASPLAKINOLIDE; DERIVATIVES; EXTRACTS; CYCLODEPSIPEPTIDE; PHALLOIDIN; WATERS;
D O I
10.1039/d3nj00459g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Jaspamide (jasplakinolide; NSC-613009) is a cytotoxic cyclic polypeptide that was initially isolated from the sponge Jaspis cf. Johnston. It displayed anti-tumor, anti-fungal and insecticidal activities, among others. Herein, an LC-MS/MS approach for the identification of jaspamide (1) and its congeners in the extracts of the sponge Jaspis diastra, collected from the Mauritius waters, is described. Based on the interpretation of LC-MS/MS data and using the proposed fragmentation pattern of jaspamide (1) as a model, jaspamide (1) and its congeners were identified in the extracts. Jaspamide (1), Q, R and Z(1) were identified in hexane and ethyl acetate extracts whereas jaspamide (1) and Z(1) were identified in the methanol extract. The cytotoxic evaluation of the extracts revealed that the ethyl acetate extract was more active than the hexane and methanol extracts with IC50 values of 1.60 +/- 0.48 mu g mL(-1) on A172, 1.71 +/- 0.42 mu g mL(-1) on TERA1, 1.05 +/- 0.02 mu g mL(-1) on DLD1 and 0.75 +/- 0.04 mu g mL(-1) on HaCaT. Subsequent fractionation of this extract by column chromatography resulted in the isolation of a precipitate (JC-1) which was characterized by 1D and 2D NMR as jaspamide (1). Semi-preparative HPLC of JC-1 resulted in a purified jaspamide (1) (JC-1P). The purity of JC-1P was determined by analytical HPLC using commercial jaspamide with a purity of =97% as the reference. JC-1P with a purity of 87.63 +/- 1.33% displayed IC50 values of 1.30 +/- 0.05 mu g mL(-1) on A172, 2.59 +/- 0.33 mu g mL(-1) on TERA1, 0.68 +/- 0.11 mu g mL(-1) on DLD1 and 0.82 +/- 0.19 mu g mL(-1) on HaCaT.
引用
收藏
页码:8854 / 8866
页数:13
相关论文
共 34 条
  • [1] Evaluation of hexane and ethyl acetate extracts of the sponge Jaspis diastra collected from Mauritius Waters on HeLa cells
    Beedessee, Girish
    Ramanjooloo, Avin
    Tiscornia, Ines
    Cresteil, Thierry
    Raghothama, Srinivasarao
    Arya, Deepak
    Rao, Shashanka
    Gowd, Konkallu Hanumae
    Bollati-Fogolin, Mariela
    Marie, Daniel E. P.
    [J]. JOURNAL OF PHARMACY AND PHARMACOLOGY, 2014, 66 (09) : 1317 - 1327
  • [2] Acetylcholinesterase-Inhibitory Activities of the Extracts from Sponges Collected in Mauritius Waters
    Beedessee, Girish
    Ramanjooloo, Avin
    Surnam-Boodhun, Rashmee
    van Soest, Robw. M.
    Marie, Daniel E. P.
    [J]. CHEMISTRY & BIODIVERSITY, 2013, 10 (03) : 442 - 451
  • [3] Cytotoxic activities of hexane, ethyl acetate and butanol extracts of marine sponges from Mauritian Waters on human cancer cell lines
    Beedessee, Girish
    Ramanjooloo, Avin
    Aubert, Genevieve
    Eloy, Laure
    Surnam-Boodhun, Rashmee
    van Soest, Rob W. M.
    Cresteil, Thierry
    Marie, Daniel E. P.
    [J]. ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY, 2012, 34 (02) : 397 - 408
  • [4] Effects of jasplakinolide on the kinetics of actin polymerization -: An explanation for certain in vivo observations
    Bubb, MR
    Spector, I
    Beyer, BB
    Fosen, KM
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (07) : 5163 - 5170
  • [5] BUBB MR, 1994, J BIOL CHEM, V269, P14869
  • [6] Recent Advances in Peptide-Based Approaches for Cancer Treatment
    Conibear, Anne C.
    Schmid, Alanca
    Kamalov, Meder
    Becker, Christian F. W.
    Bello, Claudia
    [J]. CURRENT MEDICINAL CHEMISTRY, 2020, 27 (08) : 1174 - 1205
  • [7] JASPLAKINOLIDE, A CYCLODEPSIPEPTIDE FROM THE MARINE SPONGE, JASPIS SP
    CREWS, P
    MANES, LV
    BOEHLER, M
    [J]. TETRAHEDRON LETTERS, 1986, 27 (25) : 2797 - 2800
  • [8] New Acyclic Cytotoxic Jasplakinolide Derivative from the Marine Sponge Jaspis splendens
    Ebada, Sherif S.
    Mueller, Werner E. G.
    Lin, Wenhan
    Proksch, Peter
    [J]. MARINE DRUGS, 2019, 17 (02):
  • [9] Two New Jaspamide Derivatives from the Marine Sponge Jaspis splendens
    Ebada, Sherif S.
    Wray, Victor
    de Voogd, Nicole J.
    Deng, Zhiwei
    Lin, Wenhan
    Proksch, Peter
    [J]. MARINE DRUGS, 2009, 7 (03): : 435 - 444
  • [10] EL-Shorbagi A. N., 2021, PHARMACEUTICALS-BASE, V13, P579