BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//CERN//INDICO//EN
BEGIN:VEVENT
SUMMARY:Keynote talk - Models of biological membranes: complex lipid compo
 sition and membrane proteins
DTSTART;VALUE=DATE-TIME:20211208T090000Z
DTEND;VALUE=DATE-TIME:20211208T094000Z
DTSTAMP;VALUE=DATE-TIME:20260530T094624Z
UID:indico-contribution-250-1354@lindico453.srv.lu.se
DESCRIPTION:Speakers: Alessandra  Luchini ()\nBiological membranes are mai
 nly composed of lipids and proteins. Unfortunately\, the complex compositi
 on of biological membranes prevents their direct investigation with biophy
 sical methods. Therefore\, most physico-chemical and biophysical studies o
 n biological membranes rely on simple models composed of lipid bilayers in
 cluding only 1-3 lipid species and in fewer cases membrane proteins. Among
  all\, supported lipid bilayers represent suitable systems to mimic the li
 pid component of biological membranes and allow for structural and dynamic
  investigations by means of several surface sensitive techniques. However\
 , loading membrane proteins with controlled orientation in a supported lip
 id bilayer remains a challenge in this field.[1]\nRecently\, we showed the
  preparation and characterization of lipid bilayers including either compl
 ex lipid mixtures\, i.e. lipid extract from the yeast Pichia Pastoris\, or
  membrane proteins. Supported lipid bilayers with or without membrane prot
 eins were prepared by a recently developed protocol. The method is based\n
 on the application of peptide-discs [2]\, a specific kind of nanodiscs whe
 re the protein belt is composed by self-assembled 18A peptide molecules. T
 he peptide discs can be adsorbed on the hydrophilic surface of the solid s
 upport and since the formation of the 18A belt is reversible\, they can be
  disassembled by rinsing with fresh buffer solution. We showed that this m
 ethod can successfully lead to the production of supported lipid bilayer w
 ith biologically relevant lipid compositions [3] and also to the incorpora
 tion of membrane protein with asymmetric structure\, i.e. composed by one 
 large extramembrane domain (EMD) a transmembrane domain (TMD).[4]\nReferen
 ces:\n[1] G. Fragneto et al.\, Current Opinion in Colloid & Interface Scie
 nce\, 2018\, 38\, 108-121.\n[2] S. R. Mitdgaard et al.\, Soft Matter\, 201
 4\, 10\, 738-752.\n[3] A. Luchini et al.\, Anlytical Chemistry\, 2020\, 92
 \, 1\, 1081-1088.\n[4] A. Luchini et al.\, JCIS\, 2021\, 585\, 376-385.\n\
 nhttps://lindico453.srv.lu.se/event/250/contributions/1354/
LOCATION:
URL:https://lindico453.srv.lu.se/event/250/contributions/1354/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Closing remarks
DTSTART;VALUE=DATE-TIME:20211208T111500Z
DTEND;VALUE=DATE-TIME:20211208T112000Z
DTSTAMP;VALUE=DATE-TIME:20260530T094624Z
UID:indico-contribution-250-1357@lindico453.srv.lu.se
DESCRIPTION:https://lindico453.srv.lu.se/event/250/contributions/1357/
LOCATION:
URL:https://lindico453.srv.lu.se/event/250/contributions/1357/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Keynote talk - Unraveling the gating of ligand-gated ion channels 
 through cryo-EM\, SANS\, electrophysiology & molecular simulations
DTSTART;VALUE=DATE-TIME:20211208T101000Z
DTEND;VALUE=DATE-TIME:20211208T105000Z
DTSTAMP;VALUE=DATE-TIME:20260530T094624Z
UID:indico-contribution-250-1356@lindico453.srv.lu.se
DESCRIPTION:Speakers: Erik Lindahl ()\nhttps://lindico453.srv.lu.se/event/
 250/contributions/1356/
LOCATION:
URL:https://lindico453.srv.lu.se/event/250/contributions/1356/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Contr. talk 6 - Structural investigation of TSPO translocator comb
 ining SANS and ab initio simulation
DTSTART;VALUE=DATE-TIME:20211208T095000Z
DTEND;VALUE=DATE-TIME:20211208T101000Z
DTSTAMP;VALUE=DATE-TIME:20260530T094624Z
UID:indico-contribution-250-1353@lindico453.srv.lu.se
DESCRIPTION:Speakers: Sophie Combet ()\nhttps://lindico453.srv.lu.se/event
 /250/contributions/1353/
LOCATION:
URL:https://lindico453.srv.lu.se/event/250/contributions/1353/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Contr. talk 5 - Structural Characterization of a Cholesterol-produ
 cing Enzyme - Squalene Monooxygenase
DTSTART;VALUE=DATE-TIME:20211208T084000Z
DTEND;VALUE=DATE-TIME:20211208T090000Z
DTSTAMP;VALUE=DATE-TIME:20260530T094624Z
UID:indico-contribution-250-1352@lindico453.srv.lu.se
DESCRIPTION:Speakers: Emilie Müller ()\nhttps://lindico453.srv.lu.se/even
 t/250/contributions/1352/
LOCATION:
URL:https://lindico453.srv.lu.se/event/250/contributions/1352/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Keynote talk - XFEL- and synchrotron-based serial crystallography 
 studies of the membrane-bound proton pump cytochrome c oxidase
DTSTART;VALUE=DATE-TIME:20211208T080000Z
DTEND;VALUE=DATE-TIME:20211208T084000Z
DTSTAMP;VALUE=DATE-TIME:20260530T094624Z
UID:indico-contribution-250-1351@lindico453.srv.lu.se
DESCRIPTION:Speakers: Gisela Brändén ()\nhttps://lindico453.srv.lu.se/ev
 ent/250/contributions/1351/
LOCATION:
URL:https://lindico453.srv.lu.se/event/250/contributions/1351/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Keynote talk - Time-resolved fs crystallography: Discoveries and c
 hallenges
DTSTART;VALUE=DATE-TIME:20211207T150000Z
DTEND;VALUE=DATE-TIME:20211207T154000Z
DTSTAMP;VALUE=DATE-TIME:20260530T094624Z
UID:indico-contribution-250-1349@lindico453.srv.lu.se
DESCRIPTION:Speakers: Petra Fromme ()\nhttps://lindico453.srv.lu.se/event/
 250/contributions/1349/
LOCATION:
URL:https://lindico453.srv.lu.se/event/250/contributions/1349/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Contr. talk 4 - Structural characterization of transpeptidase sort
 ase enzyme from oral pathogen Streptococcus sanguinis
DTSTART;VALUE=DATE-TIME:20211207T144000Z
DTEND;VALUE=DATE-TIME:20211207T150000Z
DTSTAMP;VALUE=DATE-TIME:20260530T094624Z
UID:indico-contribution-250-1347@lindico453.srv.lu.se
DESCRIPTION:Speakers: Smita Yadav ()\nhttps://lindico453.srv.lu.se/event/2
 50/contributions/1347/
LOCATION:
URL:https://lindico453.srv.lu.se/event/250/contributions/1347/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Contr. talk 3 - Combination of SAS techniques for modeling deterge
 nt/IMP interactions
DTSTART;VALUE=DATE-TIME:20211207T141000Z
DTEND;VALUE=DATE-TIME:20211207T143000Z
DTSTAMP;VALUE=DATE-TIME:20260530T094624Z
UID:indico-contribution-250-1346@lindico453.srv.lu.se
DESCRIPTION:Speakers: Francoise Bonneté ()\nhttps://lindico453.srv.lu.se/
 event/250/contributions/1346/
LOCATION:
URL:https://lindico453.srv.lu.se/event/250/contributions/1346/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Keynote talk - Intestinal peptide and drug uptake – a structure 
 perspective
DTSTART;VALUE=DATE-TIME:20211207T131000Z
DTEND;VALUE=DATE-TIME:20211207T135000Z
DTSTAMP;VALUE=DATE-TIME:20260530T094624Z
UID:indico-contribution-250-1345@lindico453.srv.lu.se
DESCRIPTION:Speakers: Christian Löw ()\nNutrient uptake across the lipid 
 bilayer is essential for life. Membrane transporters with specialized func
 tions have evolved to maintain the nutrient homeostasis of cells. Many of 
 those are energized by an electrochemical proton gradient. Prominent membe
 rs of such ’secondary active transport system’ are the oligopeptide tr
 ansporters PepT1 and PepT2. Both belong to the Solute Carrier Family 15 (S
 LC15)\, which is highly conserved among all phyla of life. They are known 
 to play key roles in human diseases and impact the pharmacokinetic profile
 s of orally administered drug molecules. I will highlight the approaches t
 hat allowed us to structurally characterize this transporter family. We st
 udied transporter homologs (from bacteria to humans) by structural (X-ray 
 crystallography\, SAXS\, and cryo-EM)\, biochemical and biophysical approa
 ches\, and determined the molecular basis for ligand recognition. The tran
 sporter has been captured in different conformations allowing us to obtain
  a molecular picture of the transport cycle.\n\nhttps://lindico453.srv.lu.
 se/event/250/contributions/1345/
LOCATION:
URL:https://lindico453.srv.lu.se/event/250/contributions/1345/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Contr. talk 2 - Single particle cryo-EM structure of human AQP7 ad
 opting the formation of dimer of tetramers
DTSTART;VALUE=DATE-TIME:20211207T135000Z
DTEND;VALUE=DATE-TIME:20211207T141000Z
DTSTAMP;VALUE=DATE-TIME:20260530T094624Z
UID:indico-contribution-250-1344@lindico453.srv.lu.se
DESCRIPTION:Speakers: Peng Huang ()\nhttps://lindico453.srv.lu.se/event/25
 0/contributions/1344/
LOCATION:
URL:https://lindico453.srv.lu.se/event/250/contributions/1344/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Contr. talk 1 - Design and characterization of a new generation of
  amphipols for solubilizing and stabilizing membrane proteins
DTSTART;VALUE=DATE-TIME:20211207T124500Z
DTEND;VALUE=DATE-TIME:20211207T130500Z
DTSTAMP;VALUE=DATE-TIME:20260530T094624Z
UID:indico-contribution-250-1343@lindico453.srv.lu.se
DESCRIPTION:Speakers: Manuela Zoonens ()\nhttps://lindico453.srv.lu.se/eve
 nt/250/contributions/1343/
LOCATION:
URL:https://lindico453.srv.lu.se/event/250/contributions/1343/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Keynote talk - Sample optimisation and characterisation of Membran
 e proteins
DTSTART;VALUE=DATE-TIME:20211207T120500Z
DTEND;VALUE=DATE-TIME:20211207T124500Z
DTSTAMP;VALUE=DATE-TIME:20260530T094624Z
UID:indico-contribution-250-1342@lindico453.srv.lu.se
DESCRIPTION:Speakers: Maria Marta Garcia Alai  ()\nhttps://lindico453.srv.
 lu.se/event/250/contributions/1342/
LOCATION:
URL:https://lindico453.srv.lu.se/event/250/contributions/1342/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Welcome and purpose of the workshop
DTSTART;VALUE=DATE-TIME:20211207T120000Z
DTEND;VALUE=DATE-TIME:20211207T120500Z
DTSTAMP;VALUE=DATE-TIME:20260530T094624Z
UID:indico-contribution-250-1341@lindico453.srv.lu.se
DESCRIPTION:https://lindico453.srv.lu.se/event/250/contributions/1341/
LOCATION:
URL:https://lindico453.srv.lu.se/event/250/contributions/1341/
END:VEVENT
END:VCALENDAR
