Protecting Lyophilized Escherichia coli Adenylate Kinase

Drying protein-based drugs, usually via lyophilization, can facilitate storage at ambient temperature and improve accessibility but many proteins cannot withstand drying and must be formulated with protective additives called excipients. However, mechanisms of protection are poorly understood, precl...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Molecular pharmaceutics 2024-07, Vol.21 (7), p.3634-3642
Hauptverfasser: Brom, Julia A., Petrikis, Ruta G., Nieukirk, Grace E., Bourque, Joshua, Pielak, Gary J.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 3642
container_issue 7
container_start_page 3634
container_title Molecular pharmaceutics
container_volume 21
creator Brom, Julia A.
Petrikis, Ruta G.
Nieukirk, Grace E.
Bourque, Joshua
Pielak, Gary J.
description Drying protein-based drugs, usually via lyophilization, can facilitate storage at ambient temperature and improve accessibility but many proteins cannot withstand drying and must be formulated with protective additives called excipients. However, mechanisms of protection are poorly understood, precluding rational formulation design. To better understand dry proteins and their protection, we examine Escherichia coli adenylate kinase (AdK) lyophilized alone and with the additives trehalose, maltose, bovine serum albumin, cytosolic abundant heat soluble protein D, histidine, and arginine. We apply liquid-observed vapor exchange NMR to interrogate the residue-level structure in the presence and absence of additives. We pair these observations with differential scanning calorimetry data of lyophilized samples and AdK activity assays with and without heating. We show that the amino acids do not preserve the native structure as well as sugars or proteins and that after heating the most stable additives protect activity best.
doi_str_mv 10.1021/acs.molpharmaceut.4c00356
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3061781370</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3061781370</sourcerecordid><originalsourceid>FETCH-LOGICAL-a237t-ed4e4bcc7149200cc0eaddf888758e267680d18bf4b89b16b2117254a0ecbb513</originalsourceid><addsrcrecordid>eNqNkD1PwzAQhi0EolD4CyhsLCn-TJyxqsqHqAQDzJbtXIirJC52MpRfT6qWSmxMd8Pzvqd7ELoleEYwJffaxlnrm02tQ6stDP2MW4yZyE7QBRGcpZIV9PS4Sz5BlzGuMaZcUHaOJkxKLFgmLpB8C74H27vuM1lt_aZ2jfuGMllGW0NwtnY6sb5xybyEbtvoHpIX1-kIV-is0k2E68Ocoo-H5fviKV29Pj4v5qtUU5b3KZQcuLE2J7ygGFuLQZdlJaXMhQSa5ZnEJZGm4kYWhmSGEpJTwTUGa4wgbIru9r2b4L8GiL1qXbTQNLoDP0TFcEZySViOR7TYozb4GANUahNcq8NWEax24tQoTv0Rpw7ixuzN4cxgWiiPyV9TIyD2wK5j7YfQjV__o_gHCUOBsg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3061781370</pqid></control><display><type>article</type><title>Protecting Lyophilized Escherichia coli Adenylate Kinase</title><source>MEDLINE</source><source>ACS Publications - Downers Grove, IL campus only.</source><creator>Brom, Julia A. ; Petrikis, Ruta G. ; Nieukirk, Grace E. ; Bourque, Joshua ; Pielak, Gary J.</creator><creatorcontrib>Brom, Julia A. ; Petrikis, Ruta G. ; Nieukirk, Grace E. ; Bourque, Joshua ; Pielak, Gary J.</creatorcontrib><description>Drying protein-based drugs, usually via lyophilization, can facilitate storage at ambient temperature and improve accessibility but many proteins cannot withstand drying and must be formulated with protective additives called excipients. However, mechanisms of protection are poorly understood, precluding rational formulation design. To better understand dry proteins and their protection, we examine Escherichia coli adenylate kinase (AdK) lyophilized alone and with the additives trehalose, maltose, bovine serum albumin, cytosolic abundant heat soluble protein D, histidine, and arginine. We apply liquid-observed vapor exchange NMR to interrogate the residue-level structure in the presence and absence of additives. We pair these observations with differential scanning calorimetry data of lyophilized samples and AdK activity assays with and without heating. We show that the amino acids do not preserve the native structure as well as sugars or proteins and that after heating the most stable additives protect activity best.</description><identifier>ISSN: 1543-8384</identifier><identifier>ISSN: 1543-8392</identifier><identifier>EISSN: 1543-8392</identifier><identifier>DOI: 10.1021/acs.molpharmaceut.4c00356</identifier><identifier>PMID: 38805365</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Adenylate Kinase - metabolism ; Arginine - chemistry ; Calorimetry, Differential Scanning ; Escherichia coli ; Excipients - chemistry ; Freeze Drying - methods ; Histidine - chemistry ; Magnetic Resonance Spectroscopy ; Maltose - chemistry ; Serum Albumin, Bovine - chemistry ; Trehalose - chemistry</subject><ispartof>Molecular pharmaceutics, 2024-07, Vol.21 (7), p.3634-3642</ispartof><rights>2024 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-a237t-ed4e4bcc7149200cc0eaddf888758e267680d18bf4b89b16b2117254a0ecbb513</cites><orcidid>0000-0001-6307-542X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.molpharmaceut.4c00356$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.molpharmaceut.4c00356$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2751,27055,27903,27904,56716,56766</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38805365$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brom, Julia A.</creatorcontrib><creatorcontrib>Petrikis, Ruta G.</creatorcontrib><creatorcontrib>Nieukirk, Grace E.</creatorcontrib><creatorcontrib>Bourque, Joshua</creatorcontrib><creatorcontrib>Pielak, Gary J.</creatorcontrib><title>Protecting Lyophilized Escherichia coli Adenylate Kinase</title><title>Molecular pharmaceutics</title><addtitle>Mol. Pharmaceutics</addtitle><description>Drying protein-based drugs, usually via lyophilization, can facilitate storage at ambient temperature and improve accessibility but many proteins cannot withstand drying and must be formulated with protective additives called excipients. However, mechanisms of protection are poorly understood, precluding rational formulation design. To better understand dry proteins and their protection, we examine Escherichia coli adenylate kinase (AdK) lyophilized alone and with the additives trehalose, maltose, bovine serum albumin, cytosolic abundant heat soluble protein D, histidine, and arginine. We apply liquid-observed vapor exchange NMR to interrogate the residue-level structure in the presence and absence of additives. We pair these observations with differential scanning calorimetry data of lyophilized samples and AdK activity assays with and without heating. We show that the amino acids do not preserve the native structure as well as sugars or proteins and that after heating the most stable additives protect activity best.</description><subject>Adenylate Kinase - metabolism</subject><subject>Arginine - chemistry</subject><subject>Calorimetry, Differential Scanning</subject><subject>Escherichia coli</subject><subject>Excipients - chemistry</subject><subject>Freeze Drying - methods</subject><subject>Histidine - chemistry</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Maltose - chemistry</subject><subject>Serum Albumin, Bovine - chemistry</subject><subject>Trehalose - chemistry</subject><issn>1543-8384</issn><issn>1543-8392</issn><issn>1543-8392</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkD1PwzAQhi0EolD4CyhsLCn-TJyxqsqHqAQDzJbtXIirJC52MpRfT6qWSmxMd8Pzvqd7ELoleEYwJffaxlnrm02tQ6stDP2MW4yZyE7QBRGcpZIV9PS4Sz5BlzGuMaZcUHaOJkxKLFgmLpB8C74H27vuM1lt_aZ2jfuGMllGW0NwtnY6sb5xybyEbtvoHpIX1-kIV-is0k2E68Ocoo-H5fviKV29Pj4v5qtUU5b3KZQcuLE2J7ygGFuLQZdlJaXMhQSa5ZnEJZGm4kYWhmSGEpJTwTUGa4wgbIru9r2b4L8GiL1qXbTQNLoDP0TFcEZySViOR7TYozb4GANUahNcq8NWEax24tQoTv0Rpw7ixuzN4cxgWiiPyV9TIyD2wK5j7YfQjV__o_gHCUOBsg</recordid><startdate>20240701</startdate><enddate>20240701</enddate><creator>Brom, Julia A.</creator><creator>Petrikis, Ruta G.</creator><creator>Nieukirk, Grace E.</creator><creator>Bourque, Joshua</creator><creator>Pielak, Gary J.</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-6307-542X</orcidid></search><sort><creationdate>20240701</creationdate><title>Protecting Lyophilized Escherichia coli Adenylate Kinase</title><author>Brom, Julia A. ; Petrikis, Ruta G. ; Nieukirk, Grace E. ; Bourque, Joshua ; Pielak, Gary J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a237t-ed4e4bcc7149200cc0eaddf888758e267680d18bf4b89b16b2117254a0ecbb513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adenylate Kinase - metabolism</topic><topic>Arginine - chemistry</topic><topic>Calorimetry, Differential Scanning</topic><topic>Escherichia coli</topic><topic>Excipients - chemistry</topic><topic>Freeze Drying - methods</topic><topic>Histidine - chemistry</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Maltose - chemistry</topic><topic>Serum Albumin, Bovine - chemistry</topic><topic>Trehalose - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brom, Julia A.</creatorcontrib><creatorcontrib>Petrikis, Ruta G.</creatorcontrib><creatorcontrib>Nieukirk, Grace E.</creatorcontrib><creatorcontrib>Bourque, Joshua</creatorcontrib><creatorcontrib>Pielak, Gary J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brom, Julia A.</au><au>Petrikis, Ruta G.</au><au>Nieukirk, Grace E.</au><au>Bourque, Joshua</au><au>Pielak, Gary J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protecting Lyophilized Escherichia coli Adenylate Kinase</atitle><jtitle>Molecular pharmaceutics</jtitle><addtitle>Mol. Pharmaceutics</addtitle><date>2024-07-01</date><risdate>2024</risdate><volume>21</volume><issue>7</issue><spage>3634</spage><epage>3642</epage><pages>3634-3642</pages><issn>1543-8384</issn><issn>1543-8392</issn><eissn>1543-8392</eissn><abstract>Drying protein-based drugs, usually via lyophilization, can facilitate storage at ambient temperature and improve accessibility but many proteins cannot withstand drying and must be formulated with protective additives called excipients. However, mechanisms of protection are poorly understood, precluding rational formulation design. To better understand dry proteins and their protection, we examine Escherichia coli adenylate kinase (AdK) lyophilized alone and with the additives trehalose, maltose, bovine serum albumin, cytosolic abundant heat soluble protein D, histidine, and arginine. We apply liquid-observed vapor exchange NMR to interrogate the residue-level structure in the presence and absence of additives. We pair these observations with differential scanning calorimetry data of lyophilized samples and AdK activity assays with and without heating. We show that the amino acids do not preserve the native structure as well as sugars or proteins and that after heating the most stable additives protect activity best.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>38805365</pmid><doi>10.1021/acs.molpharmaceut.4c00356</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-6307-542X</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1543-8384
ispartof Molecular pharmaceutics, 2024-07, Vol.21 (7), p.3634-3642
issn 1543-8384
1543-8392
1543-8392
language eng
recordid cdi_proquest_miscellaneous_3061781370
source MEDLINE; ACS Publications - Downers Grove, IL campus only.
subjects Adenylate Kinase - metabolism
Arginine - chemistry
Calorimetry, Differential Scanning
Escherichia coli
Excipients - chemistry
Freeze Drying - methods
Histidine - chemistry
Magnetic Resonance Spectroscopy
Maltose - chemistry
Serum Albumin, Bovine - chemistry
Trehalose - chemistry
title Protecting Lyophilized Escherichia coli Adenylate Kinase
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T19%3A30%3A52IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Protecting%20Lyophilized%20Escherichia%20coli%20Adenylate%20Kinase&rft.jtitle=Molecular%20pharmaceutics&rft.au=Brom,%20Julia%20A.&rft.date=2024-07-01&rft.volume=21&rft.issue=7&rft.spage=3634&rft.epage=3642&rft.pages=3634-3642&rft.issn=1543-8384&rft.eissn=1543-8392&rft_id=info:doi/10.1021/acs.molpharmaceut.4c00356&rft_dat=%3Cproquest_cross%3E3061781370%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3061781370&rft_id=info:pmid/38805365&rfr_iscdi=true