Thermodynamic and fibril formation studies of full length immunoglobulin light chain AL-09 and its germline protein using scan rate dependent thermal unfolding

Biophys Chem. 2015 Dec:207:13-20. doi: 10.1016/j.bpc.2015.07.005. Epub 2015 Aug 4.

Abstract

Light chain (AL) amyloidosis is a fatal disease where monoclonal immunoglobulin light chains deposit as insoluble amyloid fibrils. For many years it has been considered that AL amyloid deposits are formed primarily by the variable domain, while its constant domain has been considered not to be amyloidogenic. However recent studies identify full length (FL) light chains as part of the amyloid deposits. In this report, we compare the stabilities and amyloidogenic properties of two light chains, an amyloid-associated protein AL-09 FL, and its germline protein κ I O18/O8 FL (IGKV 1-33). We demonstrate that the thermal unfolding for both proteins is irreversible and scan rate dependent, with similar stability parameters compared to their VL counterparts. In addition, the constant domain seems to modulate their amyloidogenic properties and affect the morphology of the amyloid fibrils. These results allow us to understand the role of the kappa constant domain in AL amyloidosis.

Keywords: Amyloid fibril formation; Irreversible thermal unfolding; Kinetic stability; Light chain amyloidosis; Protein aggregation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Circular Dichroism
  • Hydrogen-Ion Concentration
  • Immunoglobulin Light Chains / chemistry*
  • Immunoglobulin Light Chains / metabolism
  • Kinetics
  • Microscopy, Electron
  • Protein Unfolding
  • Spectrophotometry, Ultraviolet
  • Temperature
  • Thermodynamics

Substances

  • Immunoglobulin Light Chains