Another publication in Nature describing the first de novo designed proteins with anti-cancer activity

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Message 90202 - Posted: 14 Jan 2019, 22:58:59 UTC



A report was published in Nature last week describing the first de novo designed proteins with anti-cancer activity.

These compact molecules were designed to stimulate the same receptors as IL-2, a powerful immunotherapeutic drug, while avoiding unwanted off-target receptor interactions. We believe this is just the first of many computer-generated cancer drugs with enhanced specificity and potency.

R@h participants provided computing for forward folding experiments used in this study which helped validate designs. We'd like to congratulate and thank all R@h volunteers who contributed to this work! Thank you!

Read the full article here: https://www.nature.com/articles/s41586-018-0830-7 (PDF)
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Message 90406 - Posted: 22 Feb 2019, 10:54:39 UTC - in response to Message 90202.  

Congratulations! Unfortunately I'd have to pay for the article to read it but based on the abstract, it sounds very cool.
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Message 90408 - Posted: 22 Feb 2019, 14:08:54 UTC - in response to Message 90406.  

Congratulations! Unfortunately I'd have to pay for the article to read it but based on the abstract, it sounds very cool.


In the news there is the link to complete pdf...
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Message 90811 - Posted: 31 May 2019, 11:26:17 UTC - in response to Message 90202.  


R@h participants provided computing for forward folding experiments used in this study which helped validate designs. We'd like to congratulate and thank all R@h volunteers who contributed to this work! Thank you!

I read through the acknowledgement section in the paper and searched for "home" in the article but failed to find any pointers to R@H. Did I not look carefully enough? I think this would be important for the project and for BOINC at large in many ways.
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Message 91097 - Posted: 7 Sep 2019, 20:00:58 UTC

This is fantastic research. I have read many articles about promising drug discoveries. It seems that many wonderful discoveries are published in esteemed journals all over the world but then and nothing seems to happen. I have lost family and friends who have been treated with drugs found 50 years ago, drugs which I gather would not now pass drug safety testing but is all we have. I have recently seen a Ted lecture by an oncologist who says that despite the many billions of dollars spent world-wide on cancer research there has been no real progress in that 50 years. As is shown by the passion of the R@h community to help, we want to support you to make a fantastic paradigm shift from stone-age medicine, but how how quickly will this fantastic work be translated into therapies at the bedside? For those poor souls at the end of their treatment line there is no time to wait!
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Message 91099 - Posted: 8 Sep 2019, 16:21:49 UTC - in response to Message 91097.  

I have recently seen a Ted lecture by an oncologist who says that despite the many billions of dollars spent world-wide on cancer research there has been no real progress in that 50 years.


I don't know who is this oncologist, but he said a lie.
Childhood tumors, for example, now have 5ys survival rate over 80%, when 30 years ago was less than 30%
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Message 91171 - Posted: 28 Sep 2019, 20:35:39 UTC

It’s good to see folding really makes difference. Hope to see more anti cancer discoveries from rah.
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Message 91617 - Posted: 26 Jan 2020, 9:04:27 UTC

It would be nice to announce this promising new in the new widget of the Rosseta@Home landing page, https://boinc.bakerlab.org/rosetta. The last published new is «The Audacious Project», 16 Jul 2019, 22:18:18 UTC.

Have a nice day, and happy crunching!
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Message 93102 - Posted: 2 Apr 2020, 18:49:46 UTC - in response to Message 90811.  

Dear steffen_moller: What a massive oversight from me! This is Daniel-Adriano Silva, author in the paper.

You are entirely right. I spend a long time in disbelief looking for the Rosetta@Home acknowledgment in the article (it should have been there), and it is missing. I am sorry, please accept my apology and let me elaborate:

In figure #1 panel "e", the bottom panel shows the use of "Forward Folding" and ("Fast Forward Folding", also known as biased Forward Folding, see Marcos et. al., https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219906/) to filter/evaluate the computational designs. We executed many of these simulations for thousands of computational designs, and many of these run on BIONC's Rosetta@Home.

The legend of Fig.1 should (instead) read as:
... e) Top: Rosetta flexible backbone sequence design; Bottom: Forward Folding simulations for filtering computational-models with smooth folding funnels (see Methods)...

The methods and/or acknowledgments do mention the use of multiple computational resources. However, they should have also included R@H, but it seems that we/I accidentally miss it. I apologize.

I hope this clarifies that R@H did contribute to this development. Please receive my acknowledgments, and know that we value your important contribution that helps us bring de novo protein to solve real-world problems.

Best,
Daniel
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Message 93103 - Posted: 2 Apr 2020, 19:10:06 UTC - in response to Message 93102.  

Dear steffen_moller: What a massive oversight from me! This is Daniel-Adriano Silva, author in the paper.

You are entirely right. I spend a long time in disbelief looking for the Rosetta@Home acknowledgment in the article (it should have been there), and it is missing. I am sorry, please accept my apology and let me elaborate:

In figure #1 panel "e", the bottom panel shows the use of "Forward Folding" and ("Fast Forward Folding", also known as biased Forward Folding, see Marcos et. al., https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219906/) to filter/evaluate the computational designs. We executed many of these simulations for thousands of computational designs, and many of these run on BIONC's Rosetta@Home.

The legend of Fig.1 should (instead) read as:
... e) Top: Rosetta flexible backbone sequence design; Bottom: Forward Folding simulations for filtering computational-models with smooth folding funnels (see Methods)...

The methods and/or acknowledgments do mention the use of multiple computational resources. However, they should have also included R@H, but it seems that we/I accidentally miss it. I apologize.

I hope this clarifies that R@H did contribute to this development. Please receive my acknowledgments, and know that we value your important contribution that helps us bring de novo protein to solve real-world problems.

Best,
Daniel


Just have to say, Daniel - wow. It takes a large amount of guts and morals to admit a wrong - especially when you could've easily ignored this and let it slide.
Thank you for your hard work, and thank you for taking the time to share this with us. You're not just working for a university or this project - you're working for humanity - and I just need to say that I genuinely appreciate it.

Keep up the good work.
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Message 99050 - Posted: 19 Sep 2020, 19:14:48 UTC
Last modified: 19 Sep 2020, 19:15:55 UTC

Read this thread, especially the links:

https://boinc.bakerlab.org/rosetta/forum_thread.php?id=14222

Neoleukin-2/15 will be entering human clinical trials either in late 2020 or mid-2021.
Hopefully, Rosetta@home will publish an update on this.
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Message 99986 - Posted: 10 Dec 2020, 21:23:15 UTC

Neoleukin Therapeutics Announces Submission of Investigational New Drug Application for NL-201 De Novo Protein Immunotherapy Candidate for Cancer

"SEATTLE, Dec. 10, 2020 (GLOBE NEWSWIRE) -- Neoleukin Therapeutics, Inc., “Neoleukin” (NASDAQ:NLTX), a biopharmaceutical company utilizing sophisticated computational methods to design de novo protein therapeutics, today announced the submission of an Investigational New Drug (IND) Application with the U.S. Food and Drug Administration to begin a Phase 1 clinical program of its lead immunotherapeutic candidate, NL-201. NL-201 is a computationally designed de novo protein that is a mimetic of natural cytokines IL-2 and IL-15."

"The Phase 1 study is expected to enroll up to 120 patients with relapsed or refractory solid tumors. Patients will receive intravenous monotherapy with NL-201 in order to assess safety, pharmacokinetics, pharmacodynamics, and antitumor activity. When the recommended dose and schedule are determined, indication-specific expansion cohorts will be enrolled to estimate safety and antitumor activity. In addition to the IND application, Neoleukin has submitted a Clinical Trial Notification (CTN) application for NL-201 in Australia."
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Message 100063 - Posted: 18 Dec 2020, 11:26:01 UTC

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Message boards : News : Another publication in Nature describing the first de novo designed proteins with anti-cancer activity



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