A novel substitution of proline (P32L) destabilises β2-microglobulin inducing hereditary systemic amyloidosis-Reference-Cited by-同舟云学术

A novel substitution of proline (P32L) destabilises β2-microglobulin inducing hereditary systemic amyloidosis

Published:2022-05-14 Issue:4 Volume:29 Page:255-262
ISSN:1350-6129
Container-title:Amyloid
language:en
Short-container-title:Amyloid

Author:

Prokaeva Tatiana¹,Joshi Tracy¹,Klimtchuk Elena S.¹,Gibson Victoria M.¹,Spencer Brian¹,Siddiqi Omar¹^ORCID,Nedelkov Dobrin²,Hu Yueming²,Berk John L.¹^ORCID,Cuddy Sarah A. M.³,Dasari Surendra⁴,Chiu April⁵,Choate Lauren A.⁵,McPhail Ellen D.⁵^ORCID,Cui Haili¹⁶,Chen Hui⁶,Burks Eric J.⁶,Sanchorawala Vaishali¹^ORCID,Connors Lawreen H.¹⁶^ORCID

Affiliation:

1. Amyloidosis Center, Boston University School of Medicine, Boston, MA, USA

2. Isoformix Inc., Phoenix, AZ, USA

3. Amyloidosis Program, Department of Medicine, Brigham and Women’s Hospital, Boston, MA, USA

4. Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA

5. Department of Laboratory of Medicine and Pathology, Mayo Clinic, Rochester, MN, USA

6. Department of Pathology and Laboratory Medicine, Boston University School of Medicine, Boston, MA, USA

Funder

Wildflower Foundation

Boston University Amyloid Research Fund

Young Family Amyloid Research Fund

Publisher

Informa UK Limited

Subject

Internal Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/13506129.2022.2072199

Reference21 articles.

1. Amyloid nomenclature 2020: update and recommendations by the International Society of Amyloidosis (ISA) nomenclature committee

2. Hereditary Systemic Amyloidosis Due to Asp76Asn Variant β2-Microglobulin

3. In vitro formation of amyloid fibrils from intact β2-microglobulin

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