PMID- 26954083 OWN - NLM STAT- MEDLINE DCOM- 20161227 LR - 20180417 IS - 1873-4367 (Electronic) IS - 0927-7765 (Linking) VI - 142 DP - 2016 Jun 1 TI - Orientating lipase molecules through surface chemical control for enhanced activity: A QCM-D and ToF-SIMS investigation. PG - 173-181 LID - S0927-7765(16)30138-2 [pii] LID - 10.1016/j.colsurfb.2016.02.059 [doi] AB - Bio-active materials consisting of lipase encapsulated within porous silica particles were engineered to control the adsorption kinetics and molecular orientation of lipase, which play critical roles in the digestion kinetics of triglycerides. The adsorption kinetics of Candida antartica lipase A (CalA) was monitored using quartz crystal microbalance with dissipation (QCM-D) and controlled by altering the hydrophobicity of a silica binding support. The extent of adsorption was 2-fold greater when CalA was adsorbed onto hydrophobic silica compared to hydrophilic silica. Time-of-flight secondary ion mass spectrometry (ToF-SIMS) fragmentation patterns, in conjunction with multivariate statistics, demonstrated enhanced exposure of the lipase's catalytic domain, specifically the histidine group responsible for activity, when CalA was adsorbed on hydrophilic silica. Consequently, lipid digestion kinetics were enhanced when CalA was loaded in hydrophilic porous silica particles, i.e., a 2-fold increase in the pseudo-first-order rate constant for digestion when compared to free lipase. In contrast, digestion kinetics were inhibited when CalA was hosted in hydrophobic porous silica, i.e., a 5-fold decrease in pseudo-first-order rate constant for digestion when compared to free lipase. These findings provide valuable insights into the mechanism of lipase action which can be exploited to develop smarter food and drug delivery systems consisting of porous lipid-based materials. CI - Copyright (c) 2016 Elsevier B.V. All rights reserved. FAU - Joyce, Paul AU - Joyce P AD - School of Pharmacy and Medical Sciences, University of South Australia, City East Campus, Adelaide, South Australia 5001, Australia. FAU - Kempson, Ivan AU - Kempson I AD - Future Industries Institute, University of South Australia, Mawson Lakes Campus, Mawson Lakes, South Australia 5095, Australia. FAU - Prestidge, Clive A AU - Prestidge CA AD - School of Pharmacy and Medical Sciences, University of South Australia, City East Campus, Adelaide, South Australia 5001, Australia. Electronic address: clive.prestidge@unisa.edu.au. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20160227 PL - Netherlands TA - Colloids Surf B Biointerfaces JT - Colloids and surfaces. B, Biointerfaces JID - 9315133 RN - 0 (Fungal Proteins) RN - 0 (Triglycerides) RN - 4QD397987E (Histidine) RN - 7631-86-9 (Silicon Dioxide) RN - EC 3.1.1.3 (Lipase) SB - IM MH - Adsorption MH - Candida/chemistry/enzymology MH - Catalytic Domain MH - Drug Compounding MH - Drug Delivery Systems MH - Fungal Proteins/*chemistry/isolation & purification MH - Histidine/chemistry MH - Hydrolysis MH - Hydrophobic and Hydrophilic Interactions MH - Kinetics MH - Lipase/*chemistry/isolation & purification MH - Porosity MH - Quartz Crystal Microbalance Techniques MH - Silicon Dioxide/*chemistry MH - Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization MH - Surface Properties MH - Triglycerides/*chemistry OTO - NOTNLM OT - Lipase OT - Lipid digestion OT - Porous silica OT - QCM-D OT - Surface chemistry OT - ToF-SIMS EDAT- 2016/03/10 06:00 MHDA- 2016/12/28 06:00 CRDT- 2016/03/09 06:00 PHST- 2015/11/06 00:00 [received] PHST- 2016/02/23 00:00 [revised] PHST- 2016/02/25 00:00 [accepted] PHST- 2016/03/09 06:00 [entrez] PHST- 2016/03/10 06:00 [pubmed] PHST- 2016/12/28 06:00 [medline] AID - S0927-7765(16)30138-2 [pii] AID - 10.1016/j.colsurfb.2016.02.059 [doi] PST - ppublish SO - Colloids Surf B Biointerfaces. 2016 Jun 1;142:173-181. doi: 10.1016/j.colsurfb.2016.02.059. Epub 2016 Feb 27.