Biomimetic recognition and peptidase activities of transition state analogue imprinted chymotrypsin mimics
Authors:
- Divya MathewDMDivya Mathew
- Benny ThomasBTBenny Thomas
- K.S. DevakyKDK.S. Devaky
- 1 March 2018
- journal article
- research article
- Published by Elsevier in Reactive and Functional Polymers
- Vol. 124, 121-128
Abstract
No abstract availableKeywords
Funding Information
- Council of Scientific and Industrial Research, India (09/499(0072)/2012-EMR-I)
This publication has 36 references indexed in Scilit:
- Recent advances in molecular imprinting technology: current status, challenges and highlighted applicationsChemical Society Reviews, 2011
- The First Example of Molecularly Imprinted Nanogels with Aldolase Type I ActivityChemistry – A European Journal, 2008
- Molecular design of novel transition state analogues for molecular imprintingNew Journal of Chemistry, 2001
- Cholesterol Esterase Activity of a Molecularly Imprinted PolymerMacromolecular Chemistry and Physics, 2001
- Influence of cross-linking monomer and hydrophobic styrene comonomer on stereoselective esterase activities of polymer catalyst imprinted with a transition-state analogue for hydrolysis of amino acid estersPolymer, 2001
- Shape- and stereo-selective esterase activities of cross-linked polymers imprinted with a transition-state analogue for the hydrolysis of amino acid estersJournal of Molecular Catalysis A: Chemical, 2001
- Molecularly imprinted polymer mimics of chymotrypsinReactive and Functional Polymers, 1999
- Molecularly Imprinted Hydrogels Exhibit Chymotrypsin-like ActivityMacromolecules, 1996
- Molecular imprinting of a transition state analogue leads to a polymer exhibiting esterolytic activityJournal of the Chemical Society, Chemical Communications, 1989
- 2-Phenylethaneboronic acid, a possible transition-state analog for chymotrypsinBiochemistry, 1971