<html xmlns:v="urn:schemas-microsoft-com:vml" xmlns:o="urn:schemas-microsoft-com:office:office" xmlns:w="urn:schemas-microsoft-com:office:word" xmlns:m="http://schemas.microsoft.com/office/2004/12/omml" xmlns="http://www.w3.org/TR/REC-html40">
<head>
<meta http-equiv="Content-Type" content="text/html; charset=us-ascii">
<meta name="Generator" content="Microsoft Word 15 (filtered medium)">
<style><!--
/* Font Definitions */
@font-face
{font-family:"Cambria Math";
panose-1:2 4 5 3 5 4 6 3 2 4;}
@font-face
{font-family:Calibri;
panose-1:2 15 5 2 2 2 4 3 2 4;}
/* Style Definitions */
p.MsoNormal, li.MsoNormal, div.MsoNormal
{margin:0in;
margin-bottom:.0001pt;
font-size:11.0pt;
font-family:"Calibri",sans-serif;}
a:link, span.MsoHyperlink
{mso-style-priority:99;
color:#0563C1;
text-decoration:underline;}
a:visited, span.MsoHyperlinkFollowed
{mso-style-priority:99;
color:#954F72;
text-decoration:underline;}
p.MsoPlainText, li.MsoPlainText, div.MsoPlainText
{mso-style-priority:99;
mso-style-link:"Plain Text Char";
margin:0in;
margin-bottom:.0001pt;
font-size:11.0pt;
font-family:"Calibri",sans-serif;}
span.PlainTextChar
{mso-style-name:"Plain Text Char";
mso-style-priority:99;
mso-style-link:"Plain Text";
font-family:"Calibri",sans-serif;}
.MsoChpDefault
{mso-style-type:export-only;
font-family:"Calibri",sans-serif;}
@page WordSection1
{size:8.5in 11.0in;
margin:1.0in 1.0in 1.0in 1.0in;}
div.WordSection1
{page:WordSection1;}
--></style><!--[if gte mso 9]><xml>
<o:shapedefaults v:ext="edit" spidmax="1026" />
</xml><![endif]--><!--[if gte mso 9]><xml>
<o:shapelayout v:ext="edit">
<o:idmap v:ext="edit" data="1" />
</o:shapelayout></xml><![endif]-->
</head>
<body lang="EN-US" link="#0563C1" vlink="#954F72">
<div class="WordSection1">
<p class="MsoPlainText">James,<o:p></o:p></p>
<p class="MsoPlainText"><o:p> </o:p></p>
<p class="MsoPlainText">Thanks for that insight. We do end up with some direct from quanitfoil and some from the US supplier (EMS in our case). But, we are having issues with both. Right now, I tried a pretty extensive cleaning (sent to me yesterday) protocol
on these quantifoil supplied grids and I have films after negative staining apoferritin. It's been a disappointing morning looking at these grids. I will definitely send these back to quantifoil and at least we know that quantifoil says we can't remove the
films once they've been shipped so we should quit trying. The worst part is that each grid is different, so in our hands checking randomly 5 out of 25 isn't enough. The two grids illustrated here are from the same side of the same grid box chosen at random
after cleaning. That's why I wanted to bake on colloidal gold fiducials on every grid so I could see if there was gold in the holes, but alas, the colloidal gold doesn't seem to want to stick to this plastic. I will also try this with different kids of gold
(maybe FAB-secondary anti-body gold will stick to this plastic). <o:p></o:p></p>
<p class="MsoPlainText"><o:p> </o:p></p>
<p class="MsoPlainText">Here's the protocol I used from Dewight Williams and Mariena Sylvestry-Ramos from when they were in Phoebe Stewart's lab:<o:p></o:p></p>
<p class="MsoPlainText"><o:p> </o:p></p>
<p class="MsoPlainText">The key to dissolving the plastic on quantifoils is to make the plastic flow away from the grid surface. When you dissolve it and it does not migrate away it just reabsorbs back on to the grid support surfaces. To get this to happen
you need to set up a thin layer chromatography system, where you have a mobile phase of solvent moving up a filter paper. We have used dichloraethane as the solvent in combination with ethyl acetate. Pre-equilibrate a glass petri dish with a saturated ethyl
acetate soaked set of Whatman filter papers with half a box of quantifoid grids, carbon side up (plastic layer down at a slight incline (we used the grid box to prop up one end. We also added a sharpie or other permanent ink spot to the filter paper before
starting to confirm we had a mobile phase which would make the dye migrate (I saw the dye migrate both times). Add to the bottom of the slightly inclined petri dish a few mls of dichloroethane. Place the lid on so the vapor will leave at the top of the inclined
petri dish (30 min). We then washed the grids in chloroform (15 min) and acetone (15 min) the same way. In the old days, we did this twice (I switched to a fresh clean glass petri dish and fresh filter paper and repeated). Then baked in a 60 C oven O/N. This
morning I glow-discharged and then negative stained apoferritin with Nano-Van.<o:p></o:p></p>
<p class="MsoPlainText"><o:p> </o:p></p>
<p class="MsoPlainText">Attached are the results. Disappointing to say the least.<o:p></o:p></p>
<p class="MsoPlainText">Looks like I keep plugging away at it. Thanks everyone for your ideas. BTW, other ideas I got were to plasma clean the grids more, but I’m kind of scared to try this as I don’t want to etch away all the carbon too!
<o:p></o:p></p>
<p class="MsoPlainText"><o:p> </o:p></p>
<p class="MsoPlainText">Cheers,<o:p></o:p></p>
<p class="MsoPlainText">Cindi L. Schwartz <o:p></o:p></p>
<p class="MsoPlainText"><o:p> </o:p></p>
<p class="MsoPlainText"><o:p> </o:p></p>
<p class="MsoPlainText">Electron Microscopist<o:p></o:p></p>
<p class="MsoPlainText">Rocky Mountain Labs/NIAID/NIH<o:p></o:p></p>
<p class="MsoPlainText">903 South 4th Street<o:p></o:p></p>
<p class="MsoPlainText">Hamilton, MT 59840<o:p></o:p></p>
<p class="MsoPlainText">406-363-9228<o:p></o:p></p>
<p class="MsoPlainText">Cindi.Schwartz@NIH.gov<o:p></o:p></p>
<p class="MsoPlainText"> Please remember our Earth before printing this email <o:p></o:p></p>
<p class="MsoPlainText">*************************************************************************<o:p></o:p></p>
<p class="MsoPlainText">The information in this e-mail and any of its attachments is confidential and may contain sensitive information. It should not be used by anyone who is not the original intended recipient. If you have received this e-mail in error please
inform the sender and delete it from your mailbox or any other storage devices. National Institute of Allergy and Infectious Diseases shall not accept liability for any statements made that are sender's own and not expressly made on behalf of the NIAID by
one of its representatives. <o:p></o:p></p>
<p class="MsoPlainText">*************************************************************************<o:p></o:p></p>
<p class="MsoPlainText"><o:p> </o:p></p>
<p class="MsoPlainText">-----Original Message-----<br>
From: Conway, James Frederick <James.Conway@pitt.edu> <br>
Sent: Tuesday, July 2, 2019 8:26 AM<br>
To: 3dem@ncmir.ucsd.edu<br>
Cc: Schwartz, Cindi (NIH/NIAID) [E] <cindi.schwartz@nih.gov><br>
Subject: Re: [3dem] Help! Plastic films on my holey grids are KILLING ME</p>
<p class="MsoPlainText"><o:p> </o:p></p>
<p class="MsoPlainText">It was my understanding that Quantifoil solved this problem quite a while back, but nonetheless we kept receiving plastic-contaminated grids from one US supplier for some time after. When I contacted Quantifoil, they said that removing
the plastic after the factory was near impossible, and when I told them the serial number of the grid boxes, they disavowed knowledge of them. My dark suspicion is that sending them back to the supplier just put them in the pipeline for someone else to receive,
but that would be rank speculation. However, buying directly from Quantifoil has resulted in near perfect grids for over 5 years now. I suggest sending the bad batches of grids back for a refund, and if you are not already dealing directly with Quantifoil,
try doing so or with a factory-recommended local supplier. If these grids are from Quantifoil, then certainly complain, send them back - it shouldn't be your time and money to fix up the grids. In my experience C-flats behave differently and (in my hands)
inconsistently, but I understand there was a period of manufacturing issues that are now resolved and I look forward to trying them again.<o:p></o:p></p>
<p class="MsoPlainText"><o:p> </o:p></p>
<p class="MsoPlainText">James Conway<o:p></o:p></p>
<p class="MsoPlainText">----------------------------------------------------------------------<o:p></o:p></p>
<p class="MsoPlainText">James Conway, PhD.,<o:p></o:p></p>
<p class="MsoPlainText">Professor, Department of Structural Biology Director, Molecular Biophysics and Structural Biology Graduate Program University of Pittsburgh School of Medicine Biomedical Science Tower 3, Room 2047<o:p></o:p></p>
<p class="MsoPlainText">3501 5th Ave<o:p></o:p></p>
<p class="MsoPlainText">Pittsburgh, PA 15213<o:p></o:p></p>
<p class="MsoPlainText">U.S.A.<o:p></o:p></p>
<p class="MsoPlainText">Phone: +1-412-383-9847<o:p></o:p></p>
<p class="MsoPlainText">Fax: +1-412-648-8998<o:p></o:p></p>
<p class="MsoPlainText">Email: <a href="mailto:jxc100@pitt.edu"><span style="color:windowtext;text-decoration:none">jxc100@pitt.edu</span></a><o:p></o:p></p>
<p class="MsoPlainText">Web: <a href="http://www.structbio.pitt.edu/index.php/12-faculty/18-james-conway">
<span style="color:windowtext;text-decoration:none">http://www.structbio.pitt.edu/index.php/12-faculty/18-james-conway</span></a>
<o:p></o:p></p>
<p class="MsoPlainText">----------------------------------------------------------------------<o:p></o:p></p>
<p class="MsoPlainText"><o:p> </o:p></p>
<p class="MsoPlainText"><o:p> </o:p></p>
<p class="MsoPlainText"><o:p> </o:p></p>
<p class="MsoPlainText"><o:p> </o:p></p>
<p class="MsoPlainText"><o:p> </o:p></p>
<p class="MsoPlainText"><o:p> </o:p></p>
<p class="MsoPlainText"><o:p> </o:p></p>
</div>
</body>
</html>