Modulation of protein biophysical properties by chemical glycosylation: biochemical insights and biomedical implications
Glycosylation constitutes one of the most important posttranslational modifications employed by biological systems to modulate protein biophysical properties. Due to the direct biochemical and biomedical implications of achieving control over protein stability and function by chemical means, there h...
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description | Glycosylation constitutes one of the most important posttranslational modifications employed by biological systems to modulate protein biophysical properties. Due to the direct biochemical and biomedical implications of achieving control over protein stability and function by chemical means, there has been great interest in recent years towards the development of chemical strategies for protein glycosylation. Since current knowledge about glycoprotein biophysics has been mainly derived from the study of naturally glycosylated proteins, chemical glycosylation provides novel insights into its mechanistic understanding by affording control over glycosylation parameters. This review presents a survey of the effects that natural and chemical glycosylation have on the fundamental biophysical properties of proteins (structure, dynamics, stability, and function). This is complemented by a mechanistic discussion of how glycans achieve such effects and discussion of the implications of employing chemical glycosylation as a tool to exert control over protein biophysical properties within biochemical and biomedical applications. |
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This review presents a survey of the effects that natural and chemical glycosylation have on the fundamental biophysical properties of proteins (structure, dynamics, stability, and function). This is complemented by a mechanistic discussion of how glycans achieve such effects and discussion of the implications of employing chemical glycosylation as a tool to exert control over protein biophysical properties within biochemical and biomedical applications.</description><identifier>ISSN: 1420-682X</identifier><identifier>EISSN: 1420-9071</identifier><identifier>DOI: 10.1007/s00018-007-6551-y</identifier><identifier>PMID: 17558468</identifier><language>eng</language><publisher>Switzerland: Basel : Birkhäuser-Verlag</publisher><subject>Animals ; Biochemistry ; Biomedical engineering ; Biophysics ; enzyme catalysis ; Enzyme Stability ; Enzymes ; glycoprotein ; Glycosylation ; Humans ; Models, Molecular ; Peptide Hydrolases - metabolism ; Polyethylene Glycols - metabolism ; protease ; Protein Conformation ; protein dynamics ; protein stability ; protein therapeutics ; Proteins ; Proteins - chemistry ; Proteins - metabolism ; Proteins - therapeutic use ; Review ; Thermodynamics</subject><ispartof>Cellular and molecular life sciences : CMLS, 2007-08, Vol.64 (16), p.2133-2152</ispartof><rights>Birkhäuser Verlag, Basel 2007</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c515t-37511b58fb4ce92db45bb036782a4c9417c471a26254142c3b7ecd8d2d6e2d413</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11138447/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11138447/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17558468$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Solá, R. J</creatorcontrib><creatorcontrib>Rodríguez-Martínez, J. A</creatorcontrib><creatorcontrib>Griebenow, K</creatorcontrib><title>Modulation of protein biophysical properties by chemical glycosylation: biochemical insights and biomedical implications</title><title>Cellular and molecular life sciences : CMLS</title><addtitle>Cell Mol Life Sci</addtitle><description>Glycosylation constitutes one of the most important posttranslational modifications employed by biological systems to modulate protein biophysical properties. Due to the direct biochemical and biomedical implications of achieving control over protein stability and function by chemical means, there has been great interest in recent years towards the development of chemical strategies for protein glycosylation. Since current knowledge about glycoprotein biophysics has been mainly derived from the study of naturally glycosylated proteins, chemical glycosylation provides novel insights into its mechanistic understanding by affording control over glycosylation parameters. This review presents a survey of the effects that natural and chemical glycosylation have on the fundamental biophysical properties of proteins (structure, dynamics, stability, and function). This is complemented by a mechanistic discussion of how glycans achieve such effects and discussion of the implications of employing chemical glycosylation as a tool to exert control over protein biophysical properties within biochemical and biomedical applications.</description><subject>Animals</subject><subject>Biochemistry</subject><subject>Biomedical engineering</subject><subject>Biophysics</subject><subject>enzyme catalysis</subject><subject>Enzyme Stability</subject><subject>Enzymes</subject><subject>glycoprotein</subject><subject>Glycosylation</subject><subject>Humans</subject><subject>Models, Molecular</subject><subject>Peptide Hydrolases - metabolism</subject><subject>Polyethylene Glycols - metabolism</subject><subject>protease</subject><subject>Protein Conformation</subject><subject>protein dynamics</subject><subject>protein stability</subject><subject>protein therapeutics</subject><subject>Proteins</subject><subject>Proteins - chemistry</subject><subject>Proteins - metabolism</subject><subject>Proteins - therapeutic use</subject><subject>Review</subject><subject>Thermodynamics</subject><issn>1420-682X</issn><issn>1420-9071</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkU2L1jAUhYMozjj6A9xoceGumpvvuhEZ_IIRFzrgLiRp-r4Z2qYmrdh_b2pfxo9VDvc-55DLQegx4BeAsXyZMcag6iJrwTnU6x10DozgusES7p60UOTbGXqQ802BuSLiPjoDybliQp2jn59iu_RmDnGsYldNKc4-jJUNcTquOTjTb7PJpzn4XNm1ckc__B4f-tXFvO7eV5vjdhXGHA7HOVdmbLfF4Nt9Pkx9EZshP0T3OtNn_-j0XqDrd2-_Xn6orz6__3j55qp2HPhcU8kBLFedZc43pLWMW4upkIoY5hoG0jEJhgjCWTnXUSu9a1VLWuFJy4BeoNd77rTY8g_nxzmZXk8pDCatOpqg_92M4agP8YcGAKoYkyXh-Skhxe-Lz7MeQna-783o45K1UCAUFbiAz_4Db-KSxnKdpkAoAdWoAsEOuRRzTr67_QpgvbWq91b1JrdW9Vo8T_6-4Y_jVGMBnu5AZ6I2hxSyvv5CMNAS0iipGP0FCnGqmQ</recordid><startdate>20070801</startdate><enddate>20070801</enddate><creator>Solá, R. 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subjects | Animals Biochemistry Biomedical engineering Biophysics enzyme catalysis Enzyme Stability Enzymes glycoprotein Glycosylation Humans Models, Molecular Peptide Hydrolases - metabolism Polyethylene Glycols - metabolism protease Protein Conformation protein dynamics protein stability protein therapeutics Proteins Proteins - chemistry Proteins - metabolism Proteins - therapeutic use Review Thermodynamics |
title | Modulation of protein biophysical properties by chemical glycosylation: biochemical insights and biomedical implications |
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