Functionalization of bacterial microcompartment shell interior with cysteine containing peptides enhances the iron and cobalt loading capacity

Bacterial microcompartments (BMCs) are prokaryotic organelles involved in several biochemical processes in bacterial cells. These cellular substructures consist of an icosahedral shell and an encapsulated enzymatic core. The outer shells of BMCs have been proposed as an attractive platform for the c...

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Published in:	Biometals Vol. 37; no. 1; pp. 267 - 274
Main Authors:	Kalnins, Gints, Bertins, Maris, Viksna, Arturs, Tars, Kaspars
Format:	Journal Article
Language:	English
Published:	Dordrecht Springer Netherlands 01.02.2024 Springer Nature B.V
Subjects:	Bacteria Bacterial Proteins - chemistry Biochemistry Biomedical and Life Sciences Brief Report Cell Biology Chromatography Cloning Cobalt Cysteine Enzymes Gas flow Iron Life Sciences Lumens Medicine/Public Health Microbiology Nanomaterials Nanotechnology Nickel Organelles Peptides Pharmacology/Toxicology Plant Physiology Proteins Shells Zinc Bacterial microcompartments Protein shells Metal-binding peptides
ISSN:	0966-0844, 1572-8773, 1572-8773
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Abstract	Bacterial microcompartments (BMCs) are prokaryotic organelles involved in several biochemical processes in bacterial cells. These cellular substructures consist of an icosahedral shell and an encapsulated enzymatic core. The outer shells of BMCs have been proposed as an attractive platform for the creation of novel nanomaterials, nanocages, and nanoreactors. In this study, we present a method for functionalizing recombinant GRM2-type BMC shell lumens with short cysteine-containing sequences and demonstrate that the iron and cobalt loading capacity of such modified shells is markedly increased. These results also imply that a passive flow of cobalt and iron atoms across the BMC shell could be possible.
AbstractList	Bacterial microcompartments (BMCs) are prokaryotic organelles involved in several biochemical processes in bacterial cells. These cellular substructures consist of an icosahedral shell and an encapsulated enzymatic core. The outer shells of BMCs have been proposed as an attractive platform for the creation of novel nanomaterials, nanocages, and nanoreactors. In this study, we present a method for functionalizing recombinant GRM2-type BMC shell lumens with short cysteine-containing sequences and demonstrate that the iron and cobalt loading capacity of such modified shells is markedly increased. These results also imply that a passive flow of cobalt and iron atoms across the BMC shell could be possible. Bacterial microcompartments (BMCs) are prokaryotic organelles involved in several biochemical processes in bacterial cells. These cellular substructures consist of an icosahedral shell and an encapsulated enzymatic core. The outer shells of BMCs have been proposed as an attractive platform for the creation of novel nanomaterials, nanocages, and nanoreactors. In this study, we present a method for functionalizing recombinant GRM2-type BMC shell lumens with short cysteine-containing sequences and demonstrate that the iron and cobalt loading capacity of such modified shells is markedly increased. These results also imply that a passive flow of cobalt and iron atoms across the BMC shell could be possible.Bacterial microcompartments (BMCs) are prokaryotic organelles involved in several biochemical processes in bacterial cells. These cellular substructures consist of an icosahedral shell and an encapsulated enzymatic core. The outer shells of BMCs have been proposed as an attractive platform for the creation of novel nanomaterials, nanocages, and nanoreactors. In this study, we present a method for functionalizing recombinant GRM2-type BMC shell lumens with short cysteine-containing sequences and demonstrate that the iron and cobalt loading capacity of such modified shells is markedly increased. These results also imply that a passive flow of cobalt and iron atoms across the BMC shell could be possible.
Author	Bertins, Maris Kalnins, Gints Tars, Kaspars Viksna, Arturs
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Cites_doi	10.1371/journal.pone.0159451 10.1016/j.tim.2014.10.003 10.1002/1521-4095(20020318)14:6<415::AID-ADMA415>3.0.CO;2-W 10.1128/AEM.02587-15 10.1016/j.ymben.2019.04.011 10.1038/nature08300 10.15252/embj.201488566 10.1016/j.mib.2021.04.007 10.3390/ijms24010456 10.1021/ar900015x 10.1038/s41467-019-14205-y 10.1038/nrmicro.2018.10 10.1021/ic991269q 10.1002/bit.10748 10.1128/MMBR.00061-12 10.1093/nar/gky427 10.1021/ic200270p 10.1038/s41467-018-05922-x 10.1093/nar/gkac714 10.1371/journal.pcbi.1003898 10.1007/s00775-016-1336-0 10.1146/annurev-biochem-040320-102858 10.1038/s41467-018-05162-z 10.1021/la203866c 10.1073/pnas.2116871119 10.1002/biot.201600415 10.1002/pro.2196 10.1093/femsle/fnx176 10.1039/c1cc11215e 10.1002/open.202000304 10.1126/science.aan3289 10.1128/MMBR.00009-14
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Keywords	Bacterial microcompartments Protein shells Metal-binding peptides
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Snippet	Bacterial microcompartments (BMCs) are prokaryotic organelles involved in several biochemical processes in bacterial cells. These cellular substructures...
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SubjectTerms	Bacteria Bacterial Proteins - chemistry Biochemistry Biomedical and Life Sciences Brief Report Cell Biology Chromatography Cloning Cobalt Cysteine Enzymes Gas flow Iron Life Sciences Lumens Medicine/Public Health Microbiology Nanomaterials Nanotechnology Nickel Organelles Peptides Pharmacology/Toxicology Plant Physiology Proteins Shells Zinc
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Title	Functionalization of bacterial microcompartment shell interior with cysteine containing peptides enhances the iron and cobalt loading capacity
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