TY - JOUR
T1 - Site-directed chemically-modified magnetic enzymes
T2 - fabrication, improvements, biotechnological applications and future prospects
AU - Shemsi, Ahsan Mushir
AU - Khanday, Firdous Ahmad
AU - Qurashi, Ahsanulhaq
AU - Khalil, Amjad
AU - Guerriero, Gea
AU - Siddiqui, Khawar Sohail
N1 - Funding Information:
The personal assistance of AMS, AQ, AK and KSS by KFUPM is acknowledged.
Publisher Copyright:
© 2019 Elsevier Inc.
PY - 2019/5/1
Y1 - 2019/5/1
N2 - Numerous enzymes of biotechnological importance have been immobilized on magnetic nanoparticles (MNP) via random multipoint attachment, resulting in a heterogeneous protein population with potential reduction in activity due to restriction of substrate access to the active site. Several chemistries are now available, where the modifier can be linked to a single specific amino acid in a protein molecule away from the active-site, thus enabling free access of the substrate. However, rarely these site-selective approaches have been applied to immobilize enzymes on nanoparticles. In this review, for the first time, we illustrate how to adapt site-directed chemical modification (SDCM) methods for immobilizing enzymes on iron-based MNP. These strategies are mainly chemical but may additionally require genetic and enzymatic methods. We critically examine each method and evaluate their scope for simple, quick, efficient, mild and economical immobilization of enzymes on MNP. The improvements in the catalytic properties of few available examples of immobilized enzymes are also discussed. We conclude the review with the applications and future prospects of site-selectively modified magnetic enzymes and potential benefits of this technology in improving enzymes, including cold-adapted homologues, modular enzymes, and CO 2 -sequestering, as well as non-iron based nanomaterials.
AB - Numerous enzymes of biotechnological importance have been immobilized on magnetic nanoparticles (MNP) via random multipoint attachment, resulting in a heterogeneous protein population with potential reduction in activity due to restriction of substrate access to the active site. Several chemistries are now available, where the modifier can be linked to a single specific amino acid in a protein molecule away from the active-site, thus enabling free access of the substrate. However, rarely these site-selective approaches have been applied to immobilize enzymes on nanoparticles. In this review, for the first time, we illustrate how to adapt site-directed chemical modification (SDCM) methods for immobilizing enzymes on iron-based MNP. These strategies are mainly chemical but may additionally require genetic and enzymatic methods. We critically examine each method and evaluate their scope for simple, quick, efficient, mild and economical immobilization of enzymes on MNP. The improvements in the catalytic properties of few available examples of immobilized enzymes are also discussed. We conclude the review with the applications and future prospects of site-selectively modified magnetic enzymes and potential benefits of this technology in improving enzymes, including cold-adapted homologues, modular enzymes, and CO 2 -sequestering, as well as non-iron based nanomaterials.
KW - Catalysis
KW - Click chemistry
KW - Cold-adapted
KW - Genetic modification
KW - Magnetic nanoparticles
KW - Metal organic framework
KW - Nanobiotechnology
KW - Native chemical ligation
KW - Protein engineering
KW - Site-selective immobilization
UR - http://www.scopus.com/inward/record.url?scp=85061777851&partnerID=8YFLogxK
U2 - 10.1016/j.biotechadv.2019.02.002
DO - 10.1016/j.biotechadv.2019.02.002
M3 - Review article
C2 - 30768953
AN - SCOPUS:85061777851
SN - 0734-9750
VL - 37
SP - 357
EP - 381
JO - Biotechnology Advances
JF - Biotechnology Advances
IS - 3
ER -