Amino group of salicylic acid exhibits enhanced inhibitory potential against insulin amyloid fibrillation with protective aptitude toward amyloid induced cytotoxicity. Issue 5 (19th January 2018)
- Record Type:
- Journal Article
- Title:
- Amino group of salicylic acid exhibits enhanced inhibitory potential against insulin amyloid fibrillation with protective aptitude toward amyloid induced cytotoxicity. Issue 5 (19th January 2018)
- Main Title:
- Amino group of salicylic acid exhibits enhanced inhibitory potential against insulin amyloid fibrillation with protective aptitude toward amyloid induced cytotoxicity
- Authors:
- Zaman, Masihuz
Khan, Mohsin Vahid
Zakariya, Syed Mohammad
Nusrat, Saima
Meeran, Syed Mustapha
Alam, Parvez
Ajmal, Mohammad Rehan
Wahiduzzaman, Wahiduzzaman
Shahein, Yasser E.
Abouelella, Amira M.
Khan, Rizwan Hasan - Abstract:
- Abstract: Protein misfolding and aggregation lead to amyloid generation that in turn may induce cell membrane disruption and leads to cell apoptosis. In an effort to prevent or treat amyloidogenesis, large number of studies has been paying attention on breakthrough of amyloid inhibitors. In the present work, we aim to access the effect of two drugs, that is, acetylsalicylic acid and 5‐amino salicylic acid on insulin amyloids by using various biophysical, imaging, cell viability assay, and computational approaches. We established that both drugs reduce the turbidity, light scattering and fluorescence intensity of amyloid indicator dye thioflavin T. Premixing of drugs with insulin inhibited the nucleation phase and inhibitory potential was boosted by increasing the concentration of the drug. Moreover, addition of drugs at the studied concentrations attenuated the insulin fibril induced cytotoxicity in breast cancer cell line MDA‐MB‐231. Our results highlight the amino group of salicylic acid exhibited enhanced inhibitory effects on insulin fibrillation in comparison to acetyl group. It may be due to presence of amino group that helps it to prolong the nucleation phase with strong binding as well as disruption of aromatic and hydrophobic stacking that plays a key role in amyloid progression. Abstract : The present study demonstrates that acetylsalicylic acid (ASA) and 5‐aminosalicylic acid (5‐ASA) inhibit fibrillation of insulin and amino group of salicylic acid was found to beAbstract: Protein misfolding and aggregation lead to amyloid generation that in turn may induce cell membrane disruption and leads to cell apoptosis. In an effort to prevent or treat amyloidogenesis, large number of studies has been paying attention on breakthrough of amyloid inhibitors. In the present work, we aim to access the effect of two drugs, that is, acetylsalicylic acid and 5‐amino salicylic acid on insulin amyloids by using various biophysical, imaging, cell viability assay, and computational approaches. We established that both drugs reduce the turbidity, light scattering and fluorescence intensity of amyloid indicator dye thioflavin T. Premixing of drugs with insulin inhibited the nucleation phase and inhibitory potential was boosted by increasing the concentration of the drug. Moreover, addition of drugs at the studied concentrations attenuated the insulin fibril induced cytotoxicity in breast cancer cell line MDA‐MB‐231. Our results highlight the amino group of salicylic acid exhibited enhanced inhibitory effects on insulin fibrillation in comparison to acetyl group. It may be due to presence of amino group that helps it to prolong the nucleation phase with strong binding as well as disruption of aromatic and hydrophobic stacking that plays a key role in amyloid progression. Abstract : The present study demonstrates that acetylsalicylic acid (ASA) and 5‐aminosalicylic acid (5‐ASA) inhibit fibrillation of insulin and amino group of salicylic acid was found to be more effective in inhibition over acetyl group. This may be due to presence of amino group on aromatic ring of 5‐ASA, which makes it more efficient in prolonging the nucleation stage of insulin aggregation through comparatively strong binding with amyloid prone region of proteins. … (more)
- Is Part Of:
- Journal of cellular biochemistry. Volume 119:Issue 5(2018)
- Journal:
- Journal of cellular biochemistry
- Issue:
- Volume 119:Issue 5(2018)
- Issue Display:
- Volume 119, Issue 5 (2018)
- Year:
- 2018
- Volume:
- 119
- Issue:
- 5
- Issue Sort Value:
- 2018-0119-0005-0000
- Page Start:
- 3945
- Page End:
- 3956
- Publication Date:
- 2018-01-19
- Subjects:
- 5‐aminosalicycylic acid -- acetylsalicylic acid -- amyloid -- cytotoxicity -- inhibition
Cytochemistry -- Periodicals
572 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4644 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jcb.26538 ↗
- Languages:
- English
- ISSNs:
- 0730-2312
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4955.010000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23375.xml