Aggrelyte‐2 promotes protein solubility and decreases lens stiffness through lysine acetylation and disulfide reduction: Implications for treating presbyopia. Issue 4 (23rd February 2023)
- Record Type:
- Journal Article
- Title:
- Aggrelyte‐2 promotes protein solubility and decreases lens stiffness through lysine acetylation and disulfide reduction: Implications for treating presbyopia. Issue 4 (23rd February 2023)
- Main Title:
- Aggrelyte‐2 promotes protein solubility and decreases lens stiffness through lysine acetylation and disulfide reduction: Implications for treating presbyopia
- Authors:
- Panja, Sudipta
Nahomi, Rooban B.
Rankenberg, Johanna
Michel, Cole R.
Gaikwad, Hanmant
Nam, Mi‐Hyun
Nagaraj, Ram H. - Abstract:
- Abstract: Aging proteins in the lens become increasingly aggregated and insoluble, contributing to presbyopia. In this study, we investigated the ability of aggrelyte‐2 (N, S‐diacetyl‐L‐cysteine methyl ester) to reverse the water insolubility of aged human lens proteins and to decrease stiffness in cultured human and mouse lenses. Water‐insoluble proteins (WI) of aged human lenses (65–75 years) were incubated with aggrelyte‐2 (500 μM) for 24 or 48 h. A control compound that lacked the S‐acetyl group (aggrelyte‐2C) was also tested. We observed 19%–30% solubility of WI upon treatment with aggrelyte‐2. Aggrelyte‐2C also increased protein solubility, but its effect was approximately 1.4‐fold lower than that of aggrelyte‐2. The protein thiol contents were 1.9‐ to 4.9‐fold higher in the aggrelyte‐2‐ and aggrelyte‐2C‐treated samples than in the untreated samples. The LC–MS/MS results showed N ε ‐acetyllysine (AcK) levels of 1.5 to 2.1 nmol/mg protein and 0.6 to 0.9 nmol/mg protein in the aggrelyte‐2‐ and aggrelyte‐2C‐treated samples. Mouse (C57BL/6J) lenses (incubated for 24 h) and human lenses (incubated for 72 h) with 1.0 mM aggrelyte‐2 showed significant decreases in stiffness with simultaneous increases in soluble proteins (human lenses) and protein‐AcK levels, and such changes were not observed in aggrelyte‐2C‐treated lenses. Mass spectrometry of the solubilized protein revealed AcK in all crystallins, but more was observed in α‐crystallins. These results suggest thatAbstract: Aging proteins in the lens become increasingly aggregated and insoluble, contributing to presbyopia. In this study, we investigated the ability of aggrelyte‐2 (N, S‐diacetyl‐L‐cysteine methyl ester) to reverse the water insolubility of aged human lens proteins and to decrease stiffness in cultured human and mouse lenses. Water‐insoluble proteins (WI) of aged human lenses (65–75 years) were incubated with aggrelyte‐2 (500 μM) for 24 or 48 h. A control compound that lacked the S‐acetyl group (aggrelyte‐2C) was also tested. We observed 19%–30% solubility of WI upon treatment with aggrelyte‐2. Aggrelyte‐2C also increased protein solubility, but its effect was approximately 1.4‐fold lower than that of aggrelyte‐2. The protein thiol contents were 1.9‐ to 4.9‐fold higher in the aggrelyte‐2‐ and aggrelyte‐2C‐treated samples than in the untreated samples. The LC–MS/MS results showed N ε ‐acetyllysine (AcK) levels of 1.5 to 2.1 nmol/mg protein and 0.6 to 0.9 nmol/mg protein in the aggrelyte‐2‐ and aggrelyte‐2C‐treated samples. Mouse (C57BL/6J) lenses (incubated for 24 h) and human lenses (incubated for 72 h) with 1.0 mM aggrelyte‐2 showed significant decreases in stiffness with simultaneous increases in soluble proteins (human lenses) and protein‐AcK levels, and such changes were not observed in aggrelyte‐2C‐treated lenses. Mass spectrometry of the solubilized protein revealed AcK in all crystallins, but more was observed in α‐crystallins. These results suggest that aggrelyte‐2 increases protein solubility and decreases lens stiffness through acetylation and disulfide reduction. Aggrelyte‐2 might be useful in treating presbyopia in humans. Abstract : Presbyopia is a major vision‐impeding problem for many people over 40. Lens hardening (stiffening), due to protein insolubilization and aggregation, significantly contributes to presbyopia. Aggrelyte‐2 solubilizes aggregated proteins and reduces lens stiffness through lysine acetylation and disulfide reduction. … (more)
- Is Part Of:
- Aging cell. Volume 22:Issue 4(2023)
- Journal:
- Aging cell
- Issue:
- Volume 22:Issue 4(2023)
- Issue Display:
- Volume 22, Issue 4 (2023)
- Year:
- 2023
- Volume:
- 22
- Issue:
- 4
- Issue Sort Value:
- 2023-0022-0004-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2023-02-23
- Subjects:
- acetylation -- disulfides -- lens -- Nε‐acetyllysine -- presbyopia -- stiffness
Cells -- Aging -- Periodicals
571.8783605 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1474-9726 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/acel.13797 ↗
- Languages:
- English
- ISSNs:
- 1474-9718
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0736.360500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 26878.xml