|
William L. Klein answers a
few questions about this month's fast breaking paper in the field of
Neuroscience & Behavior.
From
•>>February 2006
Field:
Neuroscience & Behavior
Article Title: Nanoparticle-based detection in cerebral spinal fluid of a soluble pathogenic biomarker for
Alzheimer's disease
Authors: Georganopoulou, DG;Chang, L;Nam, JM;Thaxton, CS;Mufson,
EJ;Klein,
WL;Mirkin, CA
Journal: PROC NAT ACAD SCI USA
Volume: 102
Issue: 7
Page: 2273-2276
Year: FEB 15 2005
* Northwestern Univ, Dept Neurobiol & Physiol, 2145 Sheridan Rd, Evanston, IL 60208 USA.
* Northwestern Univ, Dept Neurobiol & Physiol, Evanston, IL 60208 USA.
* Northwestern Univ, Dept Chem, Evanston, IL 60208 USA.
* Northwestern Univ, Inst Nanotechnol, Evanston, IL 60208 USA.
* Rush Univ, Med Ctr, Dept Neurol Sci, Chicago, IL 60612
USA.
|
Why
do you think your paper is highly cited?
|

“Right now, AD is diagnosed by clinical interviews and the diagnosis accuracy is less than 90%.”
|
|
Our paper is about Alzheimer’s disease (AD), and there's
tremendous interest in this subject. The story in our paper is
very novel and very significant, which is why both the National
Science Foundation and the Proceedings of the National Academy
of Sciences promoted it—and why the media coverage was high.
We offer hope of a lab test for AD—there’s none currently
available—but, with continued effort, our work potentially
could rectify that.
Does
it describe a new discovery or a new methodology that's useful to
others?
Both. Our findings establish that spinal fluid (CSF) contains
"ADDLs" (amyloid-derived diffusible ligands), which
are a new type of neurotoxin that we previously discovered and
found in brain tissue affected by Alzheimer’s. It seems
increasingly likely that ADDLs, cause AD memory loss. The new
findings show that ADDLs in CSF show a striking AD-dependence.
This suggests that ADDLs might provide, for the first time, a
real biomarker for the disease.
The methology is incredible! Our measurements depended
entirely on a novel nanotechnology invented in Chad Mirkin’s
laboratory. His "Biobarcode™" is orders of magnitude
more sensitive than the best ELISAs (Enzyme linked immunosorbent
assays) and it retains the specificity of immunassays. It can be
adapted to other diseases and applications and is a real
breakthrough. NSF has been a real force in helping to develop
this technology through its support of Northwestern’s
Nanoscale Science and Engineering Center.
Could
you summarize the significance of your paper in layman's terms?
The conclusions are exciting because they lay the foundation
for lab tests that could provide a definitive diagnosis for AD.
Right now, AD is diagnosed by clinical interviews and the
diagnosis accuracy is less than 90%.
How
did you become involved in this research, and were there successes
or failures along the way?
We discovered ADDLs a number of years ago in biochemical
experiments. When we found that ADDLs could inhibit memory
mechanisms experimentally, it became crucial to determine
whether they actually occurred in AD brain tissue. Assessment of
CSF was part of the effort. However, prior to the Biobarcode™,
we couldn't measure levels of CSF-ADDLs.
If
applicable, what are the social or political implications of your
research?
Given our aging population and the incredible financial
burden of AD, it’s going to be important to find an effective
AD treatment. As of now, none exists. We're hopeful that our
findings and methods will accelerate drug discovery by providing
reliable assessments of the disease, in addition to validating
our concepts concerning disease mechanisms.
William L. Klein
Professor of Neurobiology & Physiology
Cognitive Neurology and Alzheimer's Disease Center
Northwestern University Institute for Neuroscience
Northwestern University
Evanston, IL, USA
|
ESI Special Topics,
February 2006
Citing URL - http://www.esi-topics.com/fbp/2006/february06-WilliamLKlein.html
|
|