A simple method for mapping the location of cross-β-forming regions within protein domains of low sequence complexity

J Jinge Gu (Department of Biochemistry, University of Texas Southwestern Medical Center) X Xiaoming Zhou (School of Life Sciences) L Lillian Sutherland (Department of Biochemistry, University of Texas Southwestern Medical Center) G Glen Liszczak (Department of Biochemistry, University of Texas Southwestern Medical Center) S Steven L. McKnight (Department of Biochemistry, University of Texas Southwestern Medical Center)

Abstract

Protein domains of low sequence complexity are unable to fold into stable, three-dimensional structures. In test tube studies, these unusual polypeptide regions can self-associate in a manner causing phase separation from aqueous solution. This form of protein:protein interaction has been implicated in numerous examples of dynamic morphological organization within eukaryotic cells. In several cases, the basis for low complexity domain (LCD) self-association and phase separation has been traced to the formation of labile cross-β structures. The primary energetic force favoring formation of these transient and reversible structures is enabled by polypeptide backbone interactions. Short, contiguous networks of peptide backbone amino groups and carbonyl oxygens are zippered together intermolecularly by hydrogen bonding as described by Linus Pauling seven decades ago. Here, we describe a simple, molecular biological method useful for the identification of localized, self-associating regions within larger protein domains of low sequence complexity.

Article Details

Volume / Issue Vol. 122, Issue 17
Published April 29, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (5)

J

Jinge Gu

Department of Biochemistry, University of Texas Southwestern Medical Center

X

Xiaoming Zhou

School of Life Sciences

L

Lillian Sutherland

Department of Biochemistry, University of Texas Southwestern Medical Center

G

Glen Liszczak

Department of Biochemistry, University of Texas Southwestern Medical Center

S

Steven L. McKnight

Department of Biochemistry, University of Texas Southwestern Medical Center