An enzyme–inorganic hybrid nanoflower based immobilized enzyme reactor with enhanced enzymatic activity. Issue 11 (13th February 2015)
- Record Type:
- Journal Article
- Title:
- An enzyme–inorganic hybrid nanoflower based immobilized enzyme reactor with enhanced enzymatic activity. Issue 11 (13th February 2015)
- Main Title:
- An enzyme–inorganic hybrid nanoflower based immobilized enzyme reactor with enhanced enzymatic activity
- Authors:
- Yin, Yuqing
Xiao, Yun
Lin, Guo
Xiao, Qi
Lin, Zian
Cai, Zongwei - Abstract:
- Abstract : Ca3 (PO4 )2 –ChT hybrid nanoflowers were synthesized by a facile approach. The nanoflowers exhibited an enhanced enzymatic activity and can be used as an immobilized enzyme reactor (IMER) for highly efficient protein digestion. Abstract : A facile approach for the synthesis of enzyme–inorganic hybrid nanoflowers and their application as an immobilized α-chymotrypsin (ChT) reactor (IMER) for highly efficient protein digestion was described. The hybrid nanoflowers were room-temperature synthesized in aqueous solution using calcium phosphate (Ca3 (PO4 )2 ) as the inorganic component and ChT as the organic component. The effects of reaction parameters on the formation of the enzyme-embedded hybrid nanoflowers and their growth mechanism were investigated systematically. By monitoring the reaction of N -benzoyl-l -tyrosine ethyl ester (BTEE), the enzymatic activity of the immobilized ChT was calculated and the results showed 266% enhancement in enzymatic activity. The performance of such a nanoreactor was further demonstrated by digesting bovine serum albumin (BSA) and human serum albumin (HSA), with a stringent threshold for unambiguous identification of these digests, the yielding sequence coverages for nanoflower-based digestion were 48% and 34%, higher than those obtained with the free enzyme. The digestion time of BSA and HSA in the former case was less than 2 min, about 1/360 of that performed in the latter case (12 h). Furthermore, the residual activity of theAbstract : Ca3 (PO4 )2 –ChT hybrid nanoflowers were synthesized by a facile approach. The nanoflowers exhibited an enhanced enzymatic activity and can be used as an immobilized enzyme reactor (IMER) for highly efficient protein digestion. Abstract : A facile approach for the synthesis of enzyme–inorganic hybrid nanoflowers and their application as an immobilized α-chymotrypsin (ChT) reactor (IMER) for highly efficient protein digestion was described. The hybrid nanoflowers were room-temperature synthesized in aqueous solution using calcium phosphate (Ca3 (PO4 )2 ) as the inorganic component and ChT as the organic component. The effects of reaction parameters on the formation of the enzyme-embedded hybrid nanoflowers and their growth mechanism were investigated systematically. By monitoring the reaction of N -benzoyl-l -tyrosine ethyl ester (BTEE), the enzymatic activity of the immobilized ChT was calculated and the results showed 266% enhancement in enzymatic activity. The performance of such a nanoreactor was further demonstrated by digesting bovine serum albumin (BSA) and human serum albumin (HSA), with a stringent threshold for unambiguous identification of these digests, the yielding sequence coverages for nanoflower-based digestion were 48% and 34%, higher than those obtained with the free enzyme. The digestion time of BSA and HSA in the former case was less than 2 min, about 1/360 of that performed in the latter case (12 h). Furthermore, the residual activity of the nanoflowers decreased slightly even after eight repeated use, demonstrating promising stability. In addition, the hybrid nanoflower-based IMER was applicable to the digestion of a complex human sample, showing great promise for proteome analysis. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 3:Issue 11(2015)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 3:Issue 11(2015)
- Issue Display:
- Volume 3, Issue 11 (2015)
- Year:
- 2015
- Volume:
- 3
- Issue:
- 11
- Issue Sort Value:
- 2015-0003-0011-0000
- Page Start:
- 2295
- Page End:
- 2300
- Publication Date:
- 2015-02-13
- Subjects:
- Materials -- Periodicals
Chemistry, Analytic -- Periodicals
Biomedical materials -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/tb# ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c4tb01697a ↗
- Languages:
- English
- ISSNs:
- 2050-750X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205200
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4966.xml