Evaluating protein cross-linking as a therapeutic strategy to stabilize SOD1 variants in a mouse model of familial ALS.

Mutations in the gene encoding Cu-Zn superoxide dismutase 1 (SOD1) cause a subset of familial amyotrophic lateral sclerosis (fALS) cases. A shared effect of these mutations is that SOD1, which is normally a stable dimer, dissociates into toxic monomers that seed toxic aggregates. Considerable resear...

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Main Authors: Md Amin Hossain, Richa Sarin, Daniel P Donnelly, Brandon C Miller, Alexandra Weiss, Luke McAlary, Svetlana V Antonyuk, Joseph P Salisbury, Jakal Amin, Jeremy B Conway, Samantha S Watson, Jenifer N Winters, Yu Xu, Novera Alam, Rutali R Brahme, Haneyeh Shahbazian, Durgalakshmi Sivasankar, Swathi Padmakumar, Aziza Sattarova, Aparna C Ponmudiyan, Tanvi Gawde, David E Verrill, Wensheng Yang, Sunanda Kannapadi, Leigh D Plant, Jared R Auclair, Lee Makowski, Gregory A Petsko, Dagmar Ringe, Nathalie Y R Agar, David J Greenblatt, Mary Jo Ondrechen, Yunqiu Chen, Justin J Yerbury, Roman Manetsch, S Samar Hasnain, Robert H Brown, Jeffrey N Agar
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2024-01-01
Series:PLoS Biology
Online Access:https://journals.plos.org/plosbiology/article/file?id=10.1371/journal.pbio.3002462&type=printable
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author Md Amin Hossain
Richa Sarin
Daniel P Donnelly
Brandon C Miller
Alexandra Weiss
Luke McAlary
Svetlana V Antonyuk
Joseph P Salisbury
Jakal Amin
Jeremy B Conway
Samantha S Watson
Jenifer N Winters
Yu Xu
Novera Alam
Rutali R Brahme
Haneyeh Shahbazian
Durgalakshmi Sivasankar
Swathi Padmakumar
Aziza Sattarova
Aparna C Ponmudiyan
Tanvi Gawde
David E Verrill
Wensheng Yang
Sunanda Kannapadi
Leigh D Plant
Jared R Auclair
Lee Makowski
Gregory A Petsko
Dagmar Ringe
Nathalie Y R Agar
David J Greenblatt
Mary Jo Ondrechen
Yunqiu Chen
Justin J Yerbury
Roman Manetsch
S Samar Hasnain
Robert H Brown
Jeffrey N Agar
author_facet Md Amin Hossain
Richa Sarin
Daniel P Donnelly
Brandon C Miller
Alexandra Weiss
Luke McAlary
Svetlana V Antonyuk
Joseph P Salisbury
Jakal Amin
Jeremy B Conway
Samantha S Watson
Jenifer N Winters
Yu Xu
Novera Alam
Rutali R Brahme
Haneyeh Shahbazian
Durgalakshmi Sivasankar
Swathi Padmakumar
Aziza Sattarova
Aparna C Ponmudiyan
Tanvi Gawde
David E Verrill
Wensheng Yang
Sunanda Kannapadi
Leigh D Plant
Jared R Auclair
Lee Makowski
Gregory A Petsko
Dagmar Ringe
Nathalie Y R Agar
David J Greenblatt
Mary Jo Ondrechen
Yunqiu Chen
Justin J Yerbury
Roman Manetsch
S Samar Hasnain
Robert H Brown
Jeffrey N Agar
author_sort Md Amin Hossain
collection DOAJ
description Mutations in the gene encoding Cu-Zn superoxide dismutase 1 (SOD1) cause a subset of familial amyotrophic lateral sclerosis (fALS) cases. A shared effect of these mutations is that SOD1, which is normally a stable dimer, dissociates into toxic monomers that seed toxic aggregates. Considerable research effort has been devoted to developing compounds that stabilize the dimer of fALS SOD1 variants, but unfortunately, this has not yet resulted in a treatment. We hypothesized that cyclic thiosulfinate cross-linkers, which selectively target a rare, 2 cysteine-containing motif, can stabilize fALS-causing SOD1 variants in vivo. We created a library of chemically diverse cyclic thiosulfinates and determined structure-cross-linking-activity relationships. A pre-lead compound, "S-XL6," was selected based upon its cross-linking rate and drug-like properties. Co-crystallographic structure clearly establishes the binding of S-XL6 at Cys 111 bridging the monomers and stabilizing the SOD1 dimer. Biophysical studies reveal that the degree of stabilization afforded by S-XL6 (up to 24°C) is unprecedented for fALS, and to our knowledge, for any protein target of any kinetic stabilizer. Gene silencing and protein degrading therapeutic approaches require careful dose titration to balance the benefit of diminished fALS SOD1 expression with the toxic loss-of-enzymatic function. We show that S-XL6 does not share this liability because it rescues the activity of fALS SOD1 variants. No pharmacological agent has been proven to bind to SOD1 in vivo. Here, using a fALS mouse model, we demonstrate oral bioavailability; rapid engagement of SOD1G93A by S-XL6 that increases SOD1G93A's in vivo half-life; and that S-XL6 crosses the blood-brain barrier. S-XL6 demonstrated a degree of selectivity by avoiding off-target binding to plasma proteins. Taken together, our results indicate that cyclic thiosulfinate-mediated SOD1 stabilization should receive further attention as a potential therapeutic approach for fALS.
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spelling doaj-art-ae0b075acaa84b09a950667731983ac12025-08-20T02:49:50ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852024-01-01221e300246210.1371/journal.pbio.3002462Evaluating protein cross-linking as a therapeutic strategy to stabilize SOD1 variants in a mouse model of familial ALS.Md Amin HossainRicha SarinDaniel P DonnellyBrandon C MillerAlexandra WeissLuke McAlarySvetlana V AntonyukJoseph P SalisburyJakal AminJeremy B ConwaySamantha S WatsonJenifer N WintersYu XuNovera AlamRutali R BrahmeHaneyeh ShahbazianDurgalakshmi SivasankarSwathi PadmakumarAziza SattarovaAparna C PonmudiyanTanvi GawdeDavid E VerrillWensheng YangSunanda KannapadiLeigh D PlantJared R AuclairLee MakowskiGregory A PetskoDagmar RingeNathalie Y R AgarDavid J GreenblattMary Jo OndrechenYunqiu ChenJustin J YerburyRoman ManetschS Samar HasnainRobert H BrownJeffrey N AgarMutations in the gene encoding Cu-Zn superoxide dismutase 1 (SOD1) cause a subset of familial amyotrophic lateral sclerosis (fALS) cases. A shared effect of these mutations is that SOD1, which is normally a stable dimer, dissociates into toxic monomers that seed toxic aggregates. Considerable research effort has been devoted to developing compounds that stabilize the dimer of fALS SOD1 variants, but unfortunately, this has not yet resulted in a treatment. We hypothesized that cyclic thiosulfinate cross-linkers, which selectively target a rare, 2 cysteine-containing motif, can stabilize fALS-causing SOD1 variants in vivo. We created a library of chemically diverse cyclic thiosulfinates and determined structure-cross-linking-activity relationships. A pre-lead compound, "S-XL6," was selected based upon its cross-linking rate and drug-like properties. Co-crystallographic structure clearly establishes the binding of S-XL6 at Cys 111 bridging the monomers and stabilizing the SOD1 dimer. Biophysical studies reveal that the degree of stabilization afforded by S-XL6 (up to 24°C) is unprecedented for fALS, and to our knowledge, for any protein target of any kinetic stabilizer. Gene silencing and protein degrading therapeutic approaches require careful dose titration to balance the benefit of diminished fALS SOD1 expression with the toxic loss-of-enzymatic function. We show that S-XL6 does not share this liability because it rescues the activity of fALS SOD1 variants. No pharmacological agent has been proven to bind to SOD1 in vivo. Here, using a fALS mouse model, we demonstrate oral bioavailability; rapid engagement of SOD1G93A by S-XL6 that increases SOD1G93A's in vivo half-life; and that S-XL6 crosses the blood-brain barrier. S-XL6 demonstrated a degree of selectivity by avoiding off-target binding to plasma proteins. Taken together, our results indicate that cyclic thiosulfinate-mediated SOD1 stabilization should receive further attention as a potential therapeutic approach for fALS.https://journals.plos.org/plosbiology/article/file?id=10.1371/journal.pbio.3002462&type=printable
spellingShingle Md Amin Hossain
Richa Sarin
Daniel P Donnelly
Brandon C Miller
Alexandra Weiss
Luke McAlary
Svetlana V Antonyuk
Joseph P Salisbury
Jakal Amin
Jeremy B Conway
Samantha S Watson
Jenifer N Winters
Yu Xu
Novera Alam
Rutali R Brahme
Haneyeh Shahbazian
Durgalakshmi Sivasankar
Swathi Padmakumar
Aziza Sattarova
Aparna C Ponmudiyan
Tanvi Gawde
David E Verrill
Wensheng Yang
Sunanda Kannapadi
Leigh D Plant
Jared R Auclair
Lee Makowski
Gregory A Petsko
Dagmar Ringe
Nathalie Y R Agar
David J Greenblatt
Mary Jo Ondrechen
Yunqiu Chen
Justin J Yerbury
Roman Manetsch
S Samar Hasnain
Robert H Brown
Jeffrey N Agar
Evaluating protein cross-linking as a therapeutic strategy to stabilize SOD1 variants in a mouse model of familial ALS.
PLoS Biology
title Evaluating protein cross-linking as a therapeutic strategy to stabilize SOD1 variants in a mouse model of familial ALS.
title_full Evaluating protein cross-linking as a therapeutic strategy to stabilize SOD1 variants in a mouse model of familial ALS.
title_fullStr Evaluating protein cross-linking as a therapeutic strategy to stabilize SOD1 variants in a mouse model of familial ALS.
title_full_unstemmed Evaluating protein cross-linking as a therapeutic strategy to stabilize SOD1 variants in a mouse model of familial ALS.
title_short Evaluating protein cross-linking as a therapeutic strategy to stabilize SOD1 variants in a mouse model of familial ALS.
title_sort evaluating protein cross linking as a therapeutic strategy to stabilize sod1 variants in a mouse model of familial als
url https://journals.plos.org/plosbiology/article/file?id=10.1371/journal.pbio.3002462&type=printable
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