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...
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Veröffentlicht in: | Molecular pharmaceutics 2024-07, Vol.21 (7), p.3634-3642 |
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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 |
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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. 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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 |
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