Cytotoxicity assessment of α helix Antarctic yeast oriented antifreeze peptide (Afp1m) on M. dunni (Clone III8C) cells

In order to assess the cytotoxic effects of the cryoprotectant helix Antarctic yeast-orientated antifreeze peptide Afp1m on normal mouse skin fibroblasts, an in vitro model was developed for cytotoxicity assessment. In order to evaluate the cytotoxic effects of Afp1m, the cells of M. dunni (Clone II...

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Main Authors: Khan, Muhammad Shuaib, Abdul Rahman, Mohd Basyaruddin, Abu Bakar, Mohd Zuki, Noordin, Mohammed Mustapha, Ullah, Shakeeb, Abdul Abubakar, Adamu, Rehman, Saifur, Saddiqua, Aisha, Mohammad Yusof, Loqman
Format: Article
Language:English
Published: Universiti Putra Malaysia Press 2024
Online Access:http://psasir.upm.edu.my/id/eprint/114731/1/114731.pdf
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author Khan, Muhammad Shuaib
Abdul Rahman, Mohd Basyaruddin
Abu Bakar, Mohd Zuki
Noordin, Mohammed Mustapha
Ullah, Shakeeb
Abdul Abubakar, Adamu
Rehman, Saifur
Saddiqua, Aisha
Mohammad Yusof, Loqman
author_facet Khan, Muhammad Shuaib
Abdul Rahman, Mohd Basyaruddin
Abu Bakar, Mohd Zuki
Noordin, Mohammed Mustapha
Ullah, Shakeeb
Abdul Abubakar, Adamu
Rehman, Saifur
Saddiqua, Aisha
Mohammad Yusof, Loqman
author_sort Khan, Muhammad Shuaib
collection UPM
description In order to assess the cytotoxic effects of the cryoprotectant helix Antarctic yeast-orientated antifreeze peptide Afp1m on normal mouse skin fibroblasts, an in vitro model was developed for cytotoxicity assessment. In order to evaluate the cytotoxic effects of Afp1m, the cells of M. dunni (Clone III8C) were subjected to various amounts of Afp1m. The cell viability was assessed using MTT Assay (Tetrazolium dye MTT 3-(4, 5 dimethylthiazol-2-yl)-2, 5-10 diphenyltetrazolium bromide) against the positive control cells (Clone III8C) thatshowed 86.73 ± 6.92 % viability of cells (103.9 ± 6.56 %, 104.3 ± 5.13%, 100.9 ± 1.71%, 102.8 ± 1.24%, and 100.00 ± 0.0%). At 24, 48, and 72 hr, retarded development was noted in 10 mg/mL Afp1m. Development was observed, albeit more slowly than in the positive control and treated with lesser concentrations. The findings of this work indicate that Afp1m exhibits cryoprotective properties without inducing toxicity when used for the cryopreservation of M. dunni (Clone III8C) cells. were cul t ured wi t h 10% FBS (Foet al Bovine Serum) using an Elisa reader and in medium containing various amounts (10, 5, 2, 1 and 0.5 mg/mL) of Afp1m, the control group (10% FBS) displayed varying survival percentages (78.86 ± 10.17%, 88.38 ± 3.19%, 88.75 ± 7.19 %, 90.61 ± 7.11%, 91.19 ± 4.52%, and 100.00 ± 0.0 %) throughout 24 hr. At 72 hr of treatment, the cell viability scores of Afp1m at 5, 2, 1, and 0.5 mg/mL were significantly higher (p<0.05) than those of 10mg/mL, which showed 86.73 ± 6.92 % viability of cells (103.9 ± 6.56 %, 104.3 ± 5.13%, 100.9 ± 1.71%, 102.8 ± 1.24%, and 100.00 ± 0.0%). At 24, 48, and 72 hr, retarded development was noted in 10 mg/mL Afp1m. Development was observed, albeit more slowly than in the positive control and treated with lesser concentrations. The findings of this work indicate that Afp1m exhibits cryoprotective properties without inducing toxicity when used for the cryopreservation of M. dunni (Clone III8C) cells.
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spelling upm.eprints-1147312025-01-27T02:48:46Z http://psasir.upm.edu.my/id/eprint/114731/ Cytotoxicity assessment of α helix Antarctic yeast oriented antifreeze peptide (Afp1m) on M. dunni (Clone III8C) cells Khan, Muhammad Shuaib Abdul Rahman, Mohd Basyaruddin Abu Bakar, Mohd Zuki Noordin, Mohammed Mustapha Ullah, Shakeeb Abdul Abubakar, Adamu Rehman, Saifur Saddiqua, Aisha Mohammad Yusof, Loqman In order to assess the cytotoxic effects of the cryoprotectant helix Antarctic yeast-orientated antifreeze peptide Afp1m on normal mouse skin fibroblasts, an in vitro model was developed for cytotoxicity assessment. In order to evaluate the cytotoxic effects of Afp1m, the cells of M. dunni (Clone III8C) were subjected to various amounts of Afp1m. The cell viability was assessed using MTT Assay (Tetrazolium dye MTT 3-(4, 5 dimethylthiazol-2-yl)-2, 5-10 diphenyltetrazolium bromide) against the positive control cells (Clone III8C) thatshowed 86.73 ± 6.92 % viability of cells (103.9 ± 6.56 %, 104.3 ± 5.13%, 100.9 ± 1.71%, 102.8 ± 1.24%, and 100.00 ± 0.0%). At 24, 48, and 72 hr, retarded development was noted in 10 mg/mL Afp1m. Development was observed, albeit more slowly than in the positive control and treated with lesser concentrations. The findings of this work indicate that Afp1m exhibits cryoprotective properties without inducing toxicity when used for the cryopreservation of M. dunni (Clone III8C) cells. were cul t ured wi t h 10% FBS (Foet al Bovine Serum) using an Elisa reader and in medium containing various amounts (10, 5, 2, 1 and 0.5 mg/mL) of Afp1m, the control group (10% FBS) displayed varying survival percentages (78.86 ± 10.17%, 88.38 ± 3.19%, 88.75 ± 7.19 %, 90.61 ± 7.11%, 91.19 ± 4.52%, and 100.00 ± 0.0 %) throughout 24 hr. At 72 hr of treatment, the cell viability scores of Afp1m at 5, 2, 1, and 0.5 mg/mL were significantly higher (p<0.05) than those of 10mg/mL, which showed 86.73 ± 6.92 % viability of cells (103.9 ± 6.56 %, 104.3 ± 5.13%, 100.9 ± 1.71%, 102.8 ± 1.24%, and 100.00 ± 0.0%). At 24, 48, and 72 hr, retarded development was noted in 10 mg/mL Afp1m. Development was observed, albeit more slowly than in the positive control and treated with lesser concentrations. The findings of this work indicate that Afp1m exhibits cryoprotective properties without inducing toxicity when used for the cryopreservation of M. dunni (Clone III8C) cells. Universiti Putra Malaysia Press 2024-08-08 Article PeerReviewed text en cc_by_nc_nd_4 http://psasir.upm.edu.my/id/eprint/114731/1/114731.pdf Khan, Muhammad Shuaib and Abdul Rahman, Mohd Basyaruddin and Abu Bakar, Mohd Zuki and Noordin, Mohammed Mustapha and Ullah, Shakeeb and Abdul Abubakar, Adamu and Rehman, Saifur and Saddiqua, Aisha and Mohammad Yusof, Loqman (2024) Cytotoxicity assessment of α helix Antarctic yeast oriented antifreeze peptide (Afp1m) on M. dunni (Clone III8C) cells. Pertanika Journal of Science and Technology, 32 (5). art. no. 9. pp. 2083-2093. ISSN 0128-7680; eISSN: 2231-8526 http://www.pertanika.upm.edu.my/pjst/browse/regular-issue?article=JST-4775-2023 10.47836/pjst.32.5.09
spellingShingle Khan, Muhammad Shuaib
Abdul Rahman, Mohd Basyaruddin
Abu Bakar, Mohd Zuki
Noordin, Mohammed Mustapha
Ullah, Shakeeb
Abdul Abubakar, Adamu
Rehman, Saifur
Saddiqua, Aisha
Mohammad Yusof, Loqman
Cytotoxicity assessment of α helix Antarctic yeast oriented antifreeze peptide (Afp1m) on M. dunni (Clone III8C) cells
title Cytotoxicity assessment of α helix Antarctic yeast oriented antifreeze peptide (Afp1m) on M. dunni (Clone III8C) cells
title_full Cytotoxicity assessment of α helix Antarctic yeast oriented antifreeze peptide (Afp1m) on M. dunni (Clone III8C) cells
title_fullStr Cytotoxicity assessment of α helix Antarctic yeast oriented antifreeze peptide (Afp1m) on M. dunni (Clone III8C) cells
title_full_unstemmed Cytotoxicity assessment of α helix Antarctic yeast oriented antifreeze peptide (Afp1m) on M. dunni (Clone III8C) cells
title_short Cytotoxicity assessment of α helix Antarctic yeast oriented antifreeze peptide (Afp1m) on M. dunni (Clone III8C) cells
title_sort cytotoxicity assessment of α helix antarctic yeast oriented antifreeze peptide afp1m on m dunni clone iii8c cells
url http://psasir.upm.edu.my/id/eprint/114731/1/114731.pdf
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