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DTSTART:20260917T100000
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BEGIN:VEVENT
UID:CiviCRM_EventID_2002_e86a4f28f24ec85011f2b11344e0bb4c@onenucleus.com
SUMMARY:Webinar - Enabling Membrane Protein CryoEM\, and b
 eyond\, with Polymer Nanodiscs: A TRPML3 Case Stud
 y
X-ALT-DESC;FMTTYPE=text/html:<!DOCTYPE HTML PUBLIC
  "-//W3C//DTD HTML 3.2//EN"><html><body><p><span s
 tyle="font-size:12pt\;"><span style="font-family:A
 ptos\, sans-serif\;"><span style="font-size:11pt\;
 ">Multi-pass membrane proteins\, including GPCRs\,
  ion channels\, and transporters\, play essential 
 roles in cellular signalling\, communication\, and
  homeostasis. As the targets of many modern therap
 eutics\, they remain among the most important yet 
 challenging classes of proteins to study. Difficul
 ties in expression\, purification\, stability\, an
 d structural characterisation continue to limit pr
 ogress across both academic and industrial researc
 h.</span></span></span></p>\n \n <p><strong><span 
 style="font-size:12pt\;"><span style="font-family:
 Aptos\, sans-serif\;"><span style="font-size:11pt\
 ;">This webinar is kindly sponsored and presented 
 by...</span></span></span></strong><br />\n <img a
 lt="image-20260812094331-1.jpeg" src="https://onen
 ucleus.com/sites/default/files/civicrm/persist/con
 tribute/images/image-20260812094331-1.jpeg" style=
 "width:300px\;height:72px\;" /></p>\n \n <p><span 
 style="font-size:12pt\;"><span style="font-family:
 Aptos\, sans-serif\;"><span style="font-size:11pt\
 ;">In this webinar\, <b>Jim Reid</b> will present 
 a novel polymer nanodisc-based approach that signi
 ficantly improves the production and performance o
 f challenging membrane proteins while maintaining 
 a native-like lipid environment. By enhancing puri
 fication yields\, increasing solubility and stabil
 ity\, and reducing aggregation\, this platform ena
 bles researchers to generate high-quality membrane
  protein samples suitable for a wide range of down
 stream applications.</span></span></span></p>\n \n
  <p><span style="font-size:12pt\;"><span style="fo
 nt-family:Aptos\, sans-serif\;"><span style="font-
 size:11pt\;">The session will highlight the succes
 sful application of this technology to <b>TRPML3</
 b>\, resulting in the first detergent-free cryo-el
 ectron microscopy (cryoEM) structure of this impor
 tant ion channel. Beyond structural biology\, atte
 ndees will explore how the platform can support br
 oader biochemical\, biophysical\, and functional s
 tudies\, opening new possibilities for membrane pr
 otein research and drug discovery.</span></span></
 span></p>\n \n <p><span style="font-size:12pt\;"><
 span style="font-family:Aptos\, sans-serif\;"><spa
 n style="font-size:11pt\;">This webinar will also 
 provide an opportunity to discuss emerging applica
 tions of the technology and engage with researcher
 s interested in becoming early adopters of this in
 novative platform.</span></span></span></p>\n \n <
 p><span style="font-size:12pt\;"><span style="font
 -family:Aptos\, sans-serif\;"><b><span style="font
 -size:11pt\;">Who should attend?</span></b></span>
 </span></p>\n \n <p><span style="font-size:12pt\;"
 ><span style="font-family:Aptos\, sans-serif\;"><s
 pan style="font-size:11pt\;">This webinar is ideal
  for:</span></span></span></p>\n \n <ul>\n 	<li><s
 pan style="font-size:12pt\;"><span><span style="fo
 nt-family:Aptos\, sans-serif\;"><span style="font-
 size:11pt\;">Membrane protein researchers working 
 with GPCRs\, ion channels\, transporters\, and rel
 ated targets</span></span></span></span></li>\n 	<
 li><span style="font-size:12pt\;"><span><span styl
 e="font-family:Aptos\, sans-serif\;"><span style="
 font-size:11pt\;">Structural biologists using cryo
 EM\, crystallography\, or complementary techniques
 </span></span></span></span></li>\n 	<li><span sty
 le="font-size:12pt\;"><span><span style="font-fami
 ly:Aptos\, sans-serif\;"><span style="font-size:11
 pt\;">Scientists involved in protein expression\, 
 purification\, and characterisation</span></span><
 /span></span></li>\n 	<li><span style="font-size:1
 2pt\;"><span><span style="font-family:Aptos\, sans
 -serif\;"><span style="font-size:11pt\;">Biophysic
 ists and biochemists seeking improved membrane pro
 tein stability and sample quality</span></span></s
 pan></span></li>\n 	<li><span style="font-size:12p
 t\;"><span><span style="font-family:Aptos\, sans-s
 erif\;"><span style="font-size:11pt\;">Drug discov
 ery and therapeutic development teams targeting me
 mbrane proteins</span></span></span></span></li>\n
  	<li><span style="font-size:12pt\;"><span><span s
 tyle="font-family:Aptos\, sans-serif\;"><span styl
 e="font-size:11pt\;">Academic and industry researc
 hers exploring detergent-free methodologies</span>
 </span></span></span></li>\n </ul>\n \n <p><span s
 tyle="font-size:12pt\;"><span style="font-family:A
 ptos\, sans-serif\;"><b><span style="font-size:11p
 t\;">By attending\, participants will:</span></b><
 /span></span></p>\n \n <ul>\n 	<li><span style="fo
 nt-size:12pt\;"><span><span style="font-family:Apt
 os\, sans-serif\;"><span style="font-size:11pt\;">
 Understand the challenges associated with studying
  multi-pass membrane proteins</span></span></span>
 </span></li>\n 	<li><span style="font-size:12pt\;"
 ><span><span style="font-family:Aptos\, sans-serif
 \;"><span style="font-size:11pt\;">Learn how polym
 er nanodiscs provide a native-like\, detergent-fre
 e environment for membrane protein analysis</span>
 </span></span></span></li>\n 	<li><span style="fon
 t-size:12pt\;"><span><span style="font-family:Apto
 s\, sans-serif\;"><span style="font-size:11pt\;">D
 iscover a new approach for improving membrane prot
 ein yield\, stability\, and solubility</span></spa
 n></span></span></li>\n 	<li><span style="font-siz
 e:12pt\;"><span><span style="font-family:Aptos\, s
 ans-serif\;"><span style="font-size:11pt\;">Review
  the TRPML3 detergent-free cryoEM case study and i
 ts implications for structural biology</span></spa
 n></span></span></li>\n 	<li><span style="font-siz
 e:12pt\;"><span><span style="font-family:Aptos\, s
 ans-serif\;"><span style="font-size:11pt\;">Explor
 e applications extending beyond cryoEM into broade
 r biochemical and biophysical workflows</span></sp
 an></span></span></li>\n 	<li><span style="font-si
 ze:12pt\;"><span><span style="font-family:Aptos\, 
 sans-serif\;"><span style="font-size:11pt\;">Ident
 ify opportunities to apply this technology within 
 their own membrane protein research programmes</sp
 an></span></span></span></li>\n </ul>\n \n <p><spa
 n style="font-size:12pt\;"><span style="font-famil
 y:Aptos\, sans-serif\;"><b><span style="font-size:
 11pt\;">Join us to discover how next-generation po
 lymer nanodisc technology is helping researchers o
 vercome long-standing membrane protein challenges 
 and unlock new opportunities for structural and fu
 nctional characterisation.</span></b></span></span
 ></p>\n \n <p><strong>This webinar is:</strong></p
 >\n \n <ul>\n 	<li><strong>Free</strong> for One N
 ucleus Gold\, Partner and Corporate Sponsor/Patron
  members\;</li>\n 	<li>£30 + VAT for One Nucleus S
 ilver Members\;</li>\n 	<li>£50 + VAT for Non Memb
 ers.</li>\n </ul></body></html>
DESCRIPTION:Multi-pass membrane proteins\, including GPCRs\, i
 on channels\, and transporters\, play essential ro
 les in cellular signalling\, communication\, and h
 omeostasis. As the targets of many modern therapeu
 tics\, they remain among the most important yet ch
 allenging classes of proteins to study. Difficulti
 es in expression\, purification\, stability\, and 
 structural characterisation continue to limit prog
 ress across both academic and industrial research.
 \n \n \n \n This webinar is kindly sponsored and p
 resented by...\n \n \n \n \n \n In this webinar\, 
 Jim Reid will present a novel polymer nanodisc-bas
 ed approach that significantly improves the produc
 tion and performance of challenging membrane prote
 ins while maintaining a native-like lipid environm
 ent. By enhancing purification yields\, increasing
  solubility and stability\, and reducing aggregati
 on\, this platform enables researchers to generate
  high-quality membrane protein samples suitable fo
 r a wide range of downstream applications.\n \n \n
  \n The session will highlight the successful appl
 ication of this technology to TRPML3\, resulting i
 n the first detergent-free cryo-electron microscop
 y (cryoEM) structure of this important ion channel
 . Beyond structural biology\, attendees will explo
 re how the platform can support broader biochemica
 l\, biophysical\, and functional studies\, opening
  new possibilities for membrane protein research a
 nd drug discovery.\n \n \n \n This webinar will al
 so provide an opportunity to discuss emerging appl
 ications of the technology and engage with researc
 hers interested in becoming early adopters of this
  innovative platform.\n \n \n \n Who should attend
 ?\n \n \n \n This webinar is ideal for:\n \n \n \n
  \n 	Membrane protein researchers working with GPC
 Rs\, ion channels\, transporters\, and related tar
 gets\n 	Structural biologists using cryoEM\, cryst
 allography\, or complementary techniques\n 	Scient
 ists involved in protein expression\, purification
 \, and characterisation\n 	Biophysicists and bioch
 emists seeking improved membrane protein stability
  and sample quality\n 	Drug discovery and therapeu
 tic development teams targeting membrane proteins\
 n 	Academic and industry researchers exploring det
 ergent-free methodologies\n \n \n By attending\, p
 articipants will:\n \n \n \n \n 	Understand the ch
 allenges associated with studying multi-pass membr
 ane proteins\n 	Learn how polymer nanodiscs provid
 e a native-like\, detergent-free environment for m
 embrane protein analysis\n 	Discover a new approac
 h for improving membrane protein yield\, stability
 \, and solubility\n 	Review the TRPML3 detergent-f
 ree cryoEM case study and its implications for str
 uctural biology\n 	Explore applications extending 
 beyond cryoEM into broader biochemical and biophys
 ical workflows\n 	Identify opportunities to apply 
 this technology within their own membrane protein 
 research programmes\n \n \n Join us to discover ho
 w next-generation polymer nanodisc technology is h
 elping researchers overcome long-standing membrane
  protein challenges and unlock new opportunities f
 or structural and functional characterisation.\n \
 n \n \n This webinar is:\n \n \n \n \n 	Free for O
 ne Nucleus Gold\, Partner and Corporate Sponsor/Pa
 tron members\;\n 	£30 + VAT for One Nucleus Silver
  Members\;\n 	£50 + VAT for Non Members.\n 
CATEGORIES:Events
CALSCALE:GREGORIAN
DTSTAMP;TZID=Europe/London:20260917T100000
DTSTART;TZID=Europe/London:20260917T100000
DTEND;TZID=Europe/London:20260917T110000
LOCATION:ONLINE - webinar details will be sent to all deleg
 ates closer to the date of the event\n Cambridge\,
  \n United Kingdom\n 
URL:https://onenucleus.com/civicrm/event/info?reset=1&id=2002
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